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Mammalian Phenotype (MP): nervous system phenotype
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Phenotype Ontology
Like Gene Ontology (GO), phenotypy ontology classifies and organizes gene-mutant/null phenotypic information from the very general at the top to more specific terms in the directed acyclic graph (DAG) by viewing an individual term as a node and its relations to parental terms (allowing for multiple parents) as directed edges. To navigate this hierarchy, we display all parental phenotypic terms to the current phenotypic term of interest ordered by their shortest distances to the current term. Also, only direct children phenotypic terms of the current phenotypic term are listed. Phenotype ontologies we have incorporated are as follows:
- Disease Ontology (DO) Ontology (DO) DO semantically integrates disease and medical vocabularies through extensive cross mapping of DO terms to MeSH, ICD, NCI thesaurus, SNOMED and OMIM.
- Human Phenotype (HP) Ontology (HP) HP captures phenotypic abnormalities that are described in OMIM, along with the corresponding disease-causing genes. It includes three complementary biological concepts: Mode_of_Inheritance (MI), ONset_and_clinical_course (ON), and Phenotypic_Abnormality (PA).
- Mouse Phenotype (MP) Ontology (MP) MP describes phenotypes of the mouse after a specific gene is genetically disrupted. Using it, Mouse Genome Informatics (MGI) provides high-coverate gene-level phenotypes for the mouse.
- Worm Phenotype (WP) Ontology (WP) WP classifies and organizes phenotype descriptions for C. elegans and other nematodes. Using it, WormBase provides primary resource for phenotype annotations for C. elegans.
- Yeast Phenotype (YP) Ontology (YP) Based on YP which is the major contributor to the Ascomycete phenotype ontology, Saccharomyces Genome Database (SGD) provides single mutant phenotypes for every gene in the yeast genome.
- Fly Phenotype (FP) Ontology (FP) FP refers to FlyBase controlled vocabulary. Specifically, a structured controlled vocabulary is used for the annotation of alleles (for their mutagen etc) in FlyBase.
- Fly Anatomy (FA) Ontology (FA) FA is a structured controlled vocabulary of the anatomy of Drosophila melanogaster, used for the description of phenotypes and where a gene is expressed.
- Zebrafish Anatomy (ZA) Ontology (ZA) ZA displays anatomical terms of the zebrafish using standard anatomical nomenclature, together with affected genes.
- Xenopus Anatomy (XA) Ontology (XA) XA represents the lineage of tissues and the timing of development for frogs (Xenopus laevis and Xenopus tropicalis). It is used to annotate Xenopus gene expression patterns and mutant and morphant phenotypes.
- Arabidopsis Plant Ontology (AP) Ontology (AP) As a major contributor to Plant Ontology which describes plant anatomical and morphological structures (AN) and growth and developmental stages (DE), the Arabidopsis Information Resource (TAIR) provides arabidopsis plant ontology annotations for the model higher plant Arabidopsis thaliana.
- Enzyme Commission (EC) Ontology (EC) Each enzyme is allocated a four-digit EC number, the first three digits of which define the reaction catalysed and the fourth of which is a unique identifier (serial number). Each enzyme is also assigned a systematic name that uniquely defines the reaction catalysed.
- DrugBank ATC (DB) Ontology (DB) In the Anatomical Therapeutic Chemical (ATC) classification system, drugs are classified in groups at five different levels according to the organ or system (1st level, anatomical main group) on which they act and their therapeutic (2nd level, therapeutic subgroup), pharmacological (3rd level, pharmacological subgroup) and chemical properties (4th level, chemical subgroup; 5th level, chemical substance). Only drugs in DrugBank are considered.
- UniProtKB KeyWords (KW) Ontology (KW) Keywords in UniProtKB are controlled vocabulary, providing a summary of the entry content and are used to index UniProtKB/Swiss-Prot entries based on 10 categories (the category "Technical term" being excluded here). Each keyword is attributed manually to UniProtKB/Swiss-Prot entries and automatically to UniProtKB/TrEMBL entries (according to specific annotation rules).
- UniProtKB UniPathway (UP) Ontology (UP) UP is a fully manually curated resource for the representation and annotation of metabolic pathways, being used as controlled vocabulary for pathway annotation in UniProtKB.
Structural Domain Phenotype Ontology and its Annotations
Structural Classification of Proteins (SCOP) classifies evolutionary-related domains into Superfamily level and Family level. Using the phenotype ontologies above, we have generated the domain-centric phenotype annotations, and further identified those phenotype terms which are the most informative to annotate SCOP domains. Promisingly, domain-centric phenotypic annotations can serve as an alternative starting point to explore genotype-phenotype relationships. We provide several relevant files for the download, including the annotation and the corresponding ontology for each phenotype ontology.
- Structural Domain Disease Ontology (DO) Ontology (SDDO) and its Annotations: For details, please visit Document: PO annotation for SCOP domains, wherein Data Availability contains parsable flat files (the annotation:Domain2DO.txt, and the corresponding ontology:SDDO.txt) and mysql tables (Domain2PO.sql.gz).
- Structural Domain Human Phenotype (HP) Ontology (SDHP) and its Annotations: For details, please visit Document: PO annotation for SCOP domains, wherein Data Availability contains parsable flat files (the annotation:Domain2HP.txt, and the corresponding ontology:SDHP.txt) and mysql tables (Domain2PO.sql.gz).
- Structural Domain Mouse Phenotype (MP) Ontology (SDMP) and its Annotations: For details, please visit Document: PO annotation for SCOP domains, wherein Data Availability contains parsable flat files (the annotation:Domain2MP.txt, and the corresponding ontology:SDMP.txt) and mysql tables (Domain2PO.sql.gz).
- Structural Domain Worm Phenotype (WP) Ontology (SDWP) and its Annotations: For details, please visit Document: PO annotation for SCOP domains, wherein Data Availability contains parsable flat files (the annotation:Domain2WP.txt, and the corresponding ontology:SDWP.txt) and mysql tables (Domain2PO.sql.gz).
- Structural Domain Yeast Phenotype (YP) Ontology (SDYP) and its Annotations: For details, please visit Document: PO annotation for SCOP domains, wherein Data Availability contains parsable flat files (the annotation:Domain2YP.txt, and the corresponding ontology:SDYP.txt) and mysql tables (Domain2PO.sql.gz).
- Structural Domain Fly Phenotype (FP) Ontology (SDFP) and its Annotations: For details, please visit Document: PO annotation for SCOP domains, wherein Data Availability contains parsable flat files (the annotation:Domain2FP.txt, and the corresponding ontology:SDFP.txt) and mysql tables (Domain2PO.sql.gz).
- Structural Domain Fly Anatomy (FA) Ontology (SDFA) and its Annotations: For details, please visit Document: PO annotation for SCOP domains, wherein Data Availability contains parsable flat files (the annotation:Domain2FA.txt, and the corresponding ontology:SDFA.txt) and mysql tables (Domain2PO.sql.gz).
- Structural Domain Zebrafish Anatomy (ZA) Ontology (SDZA) and its Annotations: For details, please visit Document: PO annotation for SCOP domains, wherein Data Availability contains parsable flat files (the annotation:Domain2ZA.txt, and the corresponding ontology:SDZA.txt) and mysql tables (Domain2PO.sql.gz).
- Structural Domain Xenopus Anatomy (XA) Ontology (SDXA) and its Annotations: For details, please visit Document: PO annotation for SCOP domains, wherein Data Availability contains parsable flat files (the annotation:Domain2XA.txt, and the corresponding ontology:SDXA.txt) and mysql tables (Domain2PO.sql.gz).
- Structural Domain Arabidopsis Plant Ontology (AP) Ontology (SDAP) and its Annotations: For details, please visit Document: PO annotation for SCOP domains, wherein Data Availability contains parsable flat files (the annotation:Domain2AP.txt, and the corresponding ontology:SDAP.txt) and mysql tables (Domain2PO.sql.gz).
- Structural Domain Enzyme Commission (EC) Ontology (SDEC) and its Annotations: For details, please visit Document: PO annotation for SCOP domains, wherein Data Availability contains parsable flat files (the annotation:Domain2EC.txt, and the corresponding ontology:SDEC.txt) and mysql tables (Domain2PO.sql.gz).
- Structural Domain DrugBank ATC (DB) Ontology (SDDB) and its Annotations: For details, please visit Document: PO annotation for SCOP domains, wherein Data Availability contains parsable flat files (the annotation:Domain2DB.txt, and the corresponding ontology:SDDB.txt) and mysql tables (Domain2PO.sql.gz).
- Structural Domain UniProtKB KeyWords (KW) Ontology (SDKW) and its Annotations: For details, please visit Document: PO annotation for SCOP domains, wherein Data Availability contains parsable flat files (the annotation:Domain2KW.txt, and the corresponding ontology:SDKW.txt) and mysql tables (Domain2PO.sql.gz).
- Structural Domain UniProtKB UniPathway (UP) Ontology (SDUP) and its Annotations: For details, please visit Document: PO annotation for SCOP domains, wherein Data Availability contains parsable flat files (the annotation:Domain2UP.txt, and the corresponding ontology:SDUP.txt) and mysql tables (Domain2PO.sql.gz).
Supra-domain Phenotype Ontology and its Annotations
Although domain-centric annotations hold great promise in describing phenotypic nature of independent domains, most domains themselves may not just work alone. In multi-domain proteins, they may be combined together to form distinct domain architectures. The recombination of the existing domains is considered as one of major driving forces for phenotypic diversificaation. As an extension, we have also generated supra-domain phenotype ontology and its annotations. Compared to domain-centric phenotype ontology and annotations (SCOP domains at the Superfamily level and Family level), this version focuses on supra-domains and individual SCOP domains ONLY at the Superfamily level. Besides, in terms of individual superfamilies, their annotations from the domain-centric version may be different from those from supra-domains version. Depending on your focus, the former should be used for the consideration of both the Superfamily level and Family level, otherwise the latter should be used if you are interested in domain combinations. Also, we provide several relevant files for the download, including the annotation and the corresponding ontology for each phenotype ontology.
- Supra-domain Domain Disease Ontology (DO) Ontology (SPDO) and its Annotations: For details, please visit Document: PO annotation for Supra-domains, wherein Data Availability contains parsable flat files (the annotation:SP2DO.txt, and the corresponding ontology:SPDO.txt) and mysql tables (SP2PO.sql.gz).
- Supra-domain Domain Human Phenotype (HP) Ontology (SPHO) and its Annotations: For details, please visit Document: PO annotation for Supra-domains, wherein Data Availability contains parsable flat files (the annotation:SP2HP.txt, and the corresponding ontology:SPHO.txt) and mysql tables (SP2PO.sql.gz).
- Supra-domain Domain Mouse Phenotype (MP) Ontology (SPMP) and its Annotations: For details, please visit Document: PO annotation for Supra-domains, wherein Data Availability contains parsable flat files (the annotation:SP2MP.txt, and the corresponding ontology:SPMP.txt) and mysql tables (SP2PO.sql.gz).
- Supra-domain Domain Worm Phenotype (WP) Ontology (SPWP) and its Annotations: For details, please visit Document: PO annotation for Supra-domains, wherein Data Availability contains parsable flat files (the annotation:SP2WP.txt, and the corresponding ontology:SPWP.txt) and mysql tables (SP2PO.sql.gz).
- Supra-domain Domain Yeast Phenotype (YP) Ontology (SPYP) and its Annotations: For details, please visit Document: PO annotation for Supra-domains, wherein Data Availability contains parsable flat files (the annotation:SP2YP.txt, and the corresponding ontology:SPYP.txt) and mysql tables (SP2PO.sql.gz).
- Supra-domain Domain Fly Phenotype (FP) Ontology (SPFP) and its Annotations: For details, please visit Document: PO annotation for Supra-domains, wherein Data Availability contains parsable flat files (the annotation:SP2FP.txt, and the corresponding ontology:SPFP.txt) and mysql tables (SP2PO.sql.gz).
- Supra-domain Domain Fly Anatomy (FA) Ontology (SPFA) and its Annotations: For details, please visit Document: PO annotation for Supra-domains, wherein Data Availability contains parsable flat files (the annotation:SP2FA.txt, and the corresponding ontology:SPFA.txt) and mysql tables (SP2PO.sql.gz).
- Supra-domain Domain Zebrafish Anatomy (ZA) Ontology (SPZA) and its Annotations: For details, please visit Document: PO annotation for Supra-domains, wherein Data Availability contains parsable flat files (the annotation:SP2ZA.txt, and the corresponding ontology:SPZA.txt) and mysql tables (SP2PO.sql.gz).
- Supra-domain Domain Xenopus Anatomy (XA) Ontology (SPXA) and its Annotations: For details, please visit Document: PO annotation for Supra-domains, wherein Data Availability contains parsable flat files (the annotation:SP2XA.txt, and the corresponding ontology:SPXA.txt) and mysql tables (SP2PO.sql.gz).
- Supra-domain Domain Arabidopsis Plant Ontology (AP) Ontology (SPAP) and its Annotations: For details, please visit Document: PO annotation for Supra-domains, wherein Data Availability contains parsable flat files (the annotation:SP2AP.txt, and the corresponding ontology:SPAP.txt) and mysql tables (SP2PO.sql.gz).
- Supra-domain Domain Enzyme Commission (EC) Ontology (SPEC) and its Annotations: For details, please visit Document: PO annotation for Supra-domains, wherein Data Availability contains parsable flat files (the annotation:SP2EC.txt, and the corresponding ontology:SPEC.txt) and mysql tables (SP2PO.sql.gz).
- Supra-domain Domain DrugBank ATC (DB) Ontology (SPDB) and its Annotations: For details, please visit Document: PO annotation for Supra-domains, wherein Data Availability contains parsable flat files (the annotation:SP2DB.txt, and the corresponding ontology:SPDB.txt) and mysql tables (SP2PO.sql.gz).
- Supra-domain Domain UniProtKB KeyWords (KW) Ontology (SPKW) and its Annotations: For details, please visit Document: PO annotation for Supra-domains, wherein Data Availability contains parsable flat files (the annotation:SP2KW.txt, and the corresponding ontology:SPKW.txt) and mysql tables (SP2PO.sql.gz).
- Supra-domain Domain UniProtKB UniPathway (UP) Ontology (SPUP) and its Annotations: For details, please visit Document: PO annotation for Supra-domains, wherein Data Availability contains parsable flat files (the annotation:SP2UP.txt, and the corresponding ontology:SPUP.txt) and mysql tables (SP2PO.sql.gz).
Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]
Root: MP Hierarchy (mammalian/mouse phenotype from MGI_4.41)
Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]
Superfamily(show details)
Superfamily domains annotated to this MP term (SDMP level: Least Informative)
Highlighted in gray are those with FDR_all>0.001
SCOP term | FDR (all) | Annotation (direct or inherited) |
Composite domain of metallo-dependent hydrolases | 0 | DIRECT |
Metallothionein | 0 | DIRECT |
Nitric oxide (NO) synthase oxygenase domain | 0 | DIRECT |
Proton glutamate symport protein | 0 | DIRECT |
Tubby C-terminal domain-like | 0 | DIRECT |
E2F-DP heterodimerization region | 0 | DIRECT |
Vasodilator-stimulated phosphoprotein, VASP, tetramerisation domain | 0 | DIRECT |
Synuclein | 0 | DIRECT |
Hedgehog/DD-peptidase | 0 | DIRECT |
Hedgehog/intein (Hint) domain | 0 | DIRECT |
Lamin A/C globular tail domain | 0 | DIRECT |
Oligoxyloglucan reducing end-specific cellobiohydrolase | 0 | DIRECT |
Notch domain | 0 | DIRECT |
Homeodomain-like | 0.0000000000008705 | DIRECT |
Neurotransmitter-gated ion-channel transmembrane pore | 0.0000000003588 | DIRECT |
Nicotinic receptor ligand binding domain-like | 0.0000000003588 | DIRECT |
Periplasmic binding protein-like I | 0.00000002852 | DIRECT |
PDZ domain-like | 0.00000341 | DIRECT |
HLH, helix-loop-helix DNA-binding domain | 0.00002439 | DIRECT |
Voltage-gated potassium channels | 0.00003887 | DIRECT |
Spectrin repeat | 0.0001248 | DIRECT |
Periplasmic binding protein-like II | 0.0001259 | DIRECT |
Nuclear receptor ligand-binding domain | 0.0002279 | DIRECT |
NHL repeat | 0.0003405 | DIRECT |
Sema domain | 0.0003676 | DIRECT |
Frizzled cysteine-rich domain | 0.0005281 | DIRECT |
Plexin repeat | 0.0005589 | DIRECT |
Galactose-binding domain-like | 0.001578 | INHERITED FROM: abnormal axon guidance || abnormal brain white matter morphology || abnormal spinal cord dorsal column morphology || abnormal nervous system tract morphology |
L27 domain | 0.001741 | INHERITED FROM: abnormal excitatory postsynaptic currents |
Glucocorticoid receptor-like (DNA-binding domain) | 0.005392 | INHERITED FROM: decreased gonadotroph cell number || abnormal optic disc morphology || abnormal Rathke's pouch development |
Family A G protein-coupled receptor-like | 0.005558 | INHERITED FROM: abnormal olfactory bulb development || abnormal dopamine level || abnormal olfactory neuron innervation pattern || abnormal olfactory sensory neuron morphology |
Fibronectin type III | 0.00753 | INHERITED FROM: abnormal axon guidance |
Orange domain-like | 0.00832 | INHERITED FROM: increased neuron number || increased sensory neuron number |
Caspase-like | 0.01072 | INHERITED FROM: abnormal neuron physiology || abnormal neuron apoptosis |
YWTD domain | 0.0132 | INHERITED FROM: abnormal cerebellum morphology || amyloid beta deposits |
GAF domain-like | 0.01752 | INHERITED FROM: abnormal retinal photoreceptor morphology || decreased retinal photoreceptor cell number || decreased sensory neuron number || retinal photoreceptor degeneration || neuron degeneration |
EGF/Laminin | 0.02282 | INHERITED FROM: abnormal spinal cord ventral commissure morphology || abnormal Schwann cell morphology || abnormal spinal cord commissure morphology || fused dorsal root ganglion || increased cochlear inner hair cell number || abnormal rostral migratory stream morphology |
Concanavalin A-like lectins/glucanases | 0.02393 | INHERITED FROM: abnormal spinal cord ventral commissure morphology || abnormal paired-pulse inhibition || decreased CNS synapse formation |
C2 domain (Calcium/lipid-binding domain, CaLB) | 0.02473 | INHERITED FROM: abnormal synaptic vesicle number || abnormal synaptic vesicle morphology |
p53-like transcription factors | 0.027 | INHERITED FROM: abnormal spinal cord dorsal column morphology |
SMAD MH1 domain | 0.02868 | INHERITED FROM: abnormal nervous system development |
Cupredoxins | 0.04282 | INHERITED FROM: abnormal thalamus morphology |
SNF-like | 0.04282 | INHERITED FROM: abnormal sensorimotor gating || abnormal CNS synaptic transmission |
Doublecortin (DC) | 0.05372 | INHERITED FROM: abnormal hippocampus layer morphology || abnormal dentate gyrus morphology |
HCP-like | 0.05372 | INHERITED FROM: abnormal neural tube morphology |
SH3-domain | 0.05965 | INHERITED FROM: abnormal hippocampus pyramidal cell layer || short cochlear hair cell stereocilia || decreased excitatory postsynaptic current amplitude || abnormal synaptic vesicle recycling |
Metallo-dependent hydrolases | 0.06746 | INHERITED FROM: abnormal hippocampus layer morphology || abnormal hippocampus pyramidal cell layer || abnormal hippocampus pyramidal cell morphology || abnormal dendrite morphology |
Riboflavin synthase domain-like | 0.06746 | INHERITED FROM: decreased susceptibility to ischemic brain injury || decreased cerebral infarction size || reduced long term potentiation || abnormal blood-brain barrier function |
Ferredoxin reductase-like, C-terminal NADP-linked domain | 0.06746 | INHERITED FROM: decreased susceptibility to ischemic brain injury || decreased cerebral infarction size || reduced long term potentiation || abnormal blood-brain barrier function |
SRF-like | 0.07335 | INHERITED FROM: enhanced paired-pulse facilitation || decreased brain size || abnormal long term potentiation || abnormal neuron physiology || abnormal brain size || abnormal CNS synaptic transmission || abnormal paired-pulse facilitation |
GDNF receptor-like | 0.07335 | INHERITED FROM: abnormal somatic sensory system morphology || abnormal autonomic nervous system morphology |
HMA, heavy metal-associated domain | 0.07335 | INHERITED FROM: abnormal brain copper level |
Growth factor receptor domain | 0.08636 | INHERITED FROM: abnormal cochlear inner hair cell number || abnormal nervous system development || abnormal rostral migratory stream morphology |
lambda repressor-like DNA-binding domains | 0.08697 | INHERITED FROM: cochlear outer hair cell degeneration || abnormal neocortex morphology |
Heat shock protein 70kD (HSP70), C-terminal subdomain | 0.1066 | INHERITED FROM: altered response to CNS ischemic injury |
Clc chloride channel | 0.1066 | INHERITED FROM: abnormal retinal photoreceptor morphology || abnormal photoreceptor outer segment morphology || abnormal photoreceptor inner segment morphology |
GTPase activation domain, GAP | 0.1177 | INHERITED FROM: abnormal cerebellar granule cell morphology || ectopic cerebellar granule cells |
TIMP-like | 0.1295 | INHERITED FROM: craniorachischisis || amyloid beta deposits |
PH domain-like | 0.1546 | INHERITED FROM: abnormal brain pia mater morphology || abnormal meninges morphology |
Cysteine-rich domain | 0.1666 | INHERITED FROM: reduced long term potentiation |
Kringle-like | 0.1679 | INHERITED FROM: altered response to CNS ischemic injury |
Cystine-knot cytokines | 0.1682 | INHERITED FROM: abnormal petrosal ganglion morphology || small petrosal ganglion || small nodose ganglion || small geniculate ganglion || abnormal autonomic nervous system morphology || abnormal L4 dorsal root ganglion morphology || abnormal paravertebral ganglion morphology || small trigeminal ganglion || abnormal superior cervical ganglion morphology |
L domain-like | 0.1702 | INHERITED FROM: abnormal spinal cord ventral commissure morphology || abnormal nervous system regeneration || abnormal spinal cord lateral column morphology |
Bcl-2 inhibitors of programmed cell death | 0.1727 | INHERITED FROM: abnormal autonomic nervous system morphology |
Cap-Gly domain | 0.1749 | INHERITED FROM: abnormal motor neuron morphology || abnormal spinal cord grey matter morphology |
Flavoproteins | 0.1749 | INHERITED FROM: abnormal seizure response to inducing agent |
Cadherin-like | 0.1898 | INHERITED FROM: abnormal outer hair cell stereociliary bundle morphology || abnormal orientation of cochlear hair cell stereociliary bundles || abnormal cochlear hair cell stereociliary bundle morphology || abnormal orientation of outer hair cell stereociliary bundles || abnormal cochlear outer hair cell morphology |
SNARE fusion complex | 0.1911 | INHERITED FROM: enhanced paired-pulse facilitation || abnormal neurotransmitter secretion || abnormal axon extension |
cAMP-binding domain-like | 0.1947 | INHERITED FROM: abnormal olfactory bulb glomerular layer morphology |
4-helical cytokines | 0.237 | INHERITED FROM: increased pituitary gland tumor incidence || abnormal glial cell physiology |
Cyclin-like | 0.239 | INHERITED FROM: abnormal cerebellar Purkinje cell layer || small cerebellum || decreased retinal ganglion cell number || absent Purkinje cell layer || abnormal cerebellar layer morphology |
Zn-dependent exopeptidases | 0.2599 | INHERITED FROM: abnormal prepulse inhibition || decreased prepulse inhibition |
Immunoglobulin | 0.2599 | INHERITED FROM: abnormal innervation |
Formate/glycerate dehydrogenase catalytic domain-like | 0.2766 | INHERITED FROM: abnormal embryonic neuroepithelium morphology |
CBS-domain pair | 0.3016 | INHERITED FROM: abnormal photoreceptor outer segment morphology || increased astrocyte number || abnormal astrocyte number || abnormal photoreceptor inner segment morphology |
Second domain of FERM | 0.3119 | INHERITED FROM: abnormal inner hair cell stereociliary bundle morphology || short cochlear hair cell stereocilia |
Integrin domains | 0.4386 | INHERITED FROM: abnormal sciatic nerve morphology |
SAM/Pointed domain | 0.4815 | INHERITED FROM: abnormal axon pruning |
Spermadhesin, CUB domain | 0.4875 | INHERITED FROM: short excitatory postsynaptic current rise time || abnormal excitatory postsynaptic currents || biphasic excitatory postsynaptic current amplitude || decreased excitatory postsynaptic current amplitude || abnormal Purkinje cell innervation |
PLP-dependent transferases | 0.5056 | INHERITED FROM: abnormal neurotransmitter level |
MFS general substrate transporter | 0.5266 | INHERITED FROM: abnormal neurotransmitter uptake |
HD-domain/PDEase-like | 0.5442 | INHERITED FROM: decreased retinal photoreceptor cell number || retinal photoreceptor degeneration |
BAR/IMD domain-like | 0.5735 | INHERITED FROM: abnormal synaptic vesicle number || decreased excitatory postsynaptic current amplitude || abnormal synaptic vesicle recycling || abnormal excitatory postsynaptic current amplitude |
HMG-box | 0.6039 | INHERITED FROM: abnormal sympathetic neuron morphology || optic nerve hypoplasia || abnormal paravertebral ganglion morphology || abnormal superior cervical ganglion morphology |
TNF receptor-like | 0.6055 | INHERITED FROM: abnormal nervous system regeneration |
Toll/Interleukin receptor TIR domain | 0.6217 | INHERITED FROM: abnormal glial cell physiology |
Bromodomain | 0.6471 | INHERITED FROM: abnormal neural tube closure |
PreATP-grasp domain | 0.6708 | INHERITED FROM: abnormal synaptic depression || environmentally induced seizures || abnormal brain wave pattern || convulsive seizures || tonic-clonic seizures || increased synaptic depression || abnormal seizure response to inducing agent |
Intermediate filament protein, coiled coil region | 0.7143 | INHERITED FROM: abnormal spinal nerve morphology |
Complement control module/SCR domain | 0.7397 | INHERITED FROM: short excitatory postsynaptic current rise time || biphasic excitatory postsynaptic current amplitude || decreased excitatory postsynaptic current amplitude || abnormal Purkinje cell innervation |
FAD/NAD(P)-binding domain | 0.773 | INHERITED FROM: increased dopamine level |
ABC transporter transmembrane region | 0.8399 | INHERITED FROM: amyloid beta deposits || nervous system inclusion bodies |
Glutathione synthetase ATP-binding domain-like | 0.8774 | INHERITED FROM: environmentally induced seizures || abnormal brain wave pattern || tonic-clonic seizures || increased synaptic depression |
SAP domain | 0.8903 | INHERITED FROM: abnormal striatum morphology || abnormal basal ganglion morphology |
beta-beta-alpha zinc fingers | 0.9352 | INHERITED FROM: abnormal olfactory nerve morphology |
alpha/beta-Hydrolases | 0.9748 | INHERITED FROM: abnormal synaptic bouton morphology || abnormal central pattern generator function || abnormal pre-Botzinger complex physiology |
RNA-binding domain, RBD | 0.9999 | INHERITED FROM: premature neuronal precursor differentiation |
Cysteine proteinases | 1 | INHERITED FROM: axonal dystrophy |
SCOP term | FDR (all) | Annotation (direct or inherited) |
Composite domain of metallo-dependent hydrolases | 0 | Direct |
Metallothionein | 0 | Direct |
Nitric oxide (NO) synthase oxygenase domain | 0 | Direct |
Proton glutamate symport protein | 0 | Direct |
Tubby C-terminal domain-like | 0 | Direct |
E2F-DP heterodimerization region | 0 | Direct |
Vasodilator-stimulated phosphoprotein, VASP, tetramerisation domain | 0 | Direct |
Synuclein | 0 | Direct |
Hedgehog/DD-peptidase | 0 | Direct |
Hedgehog/intein (Hint) domain | 0 | Direct |
Lamin A/C globular tail domain | 0 | Direct |
Oligoxyloglucan reducing end-specific cellobiohydrolase | 0 | Direct |
Notch domain | 0 | Direct |
Homeodomain-like | 0.0000000000008705 | Direct |
Neurotransmitter-gated ion-channel transmembrane pore | 0.0000000003588 | Direct |
Nicotinic receptor ligand binding domain-like | 0.0000000003588 | Direct |
Periplasmic binding protein-like I | 0.00000002852 | Direct |
PDZ domain-like | 0.00000341 | Direct |
HLH, helix-loop-helix DNA-binding domain | 0.00002439 | Direct |
Voltage-gated potassium channels | 0.00003887 | Direct |
Spectrin repeat | 0.0001248 | Direct |
Periplasmic binding protein-like II | 0.0001259 | Direct |
Nuclear receptor ligand-binding domain | 0.0002279 | Direct |
NHL repeat | 0.0003405 | Direct |
Sema domain | 0.0003676 | Direct |
Frizzled cysteine-rich domain | 0.0005281 | Direct |
Plexin repeat | 0.0005589 | Direct |
Galactose-binding domain-like | 0.001578 | Inherited |
L27 domain | 0.001741 | Inherited |
Glucocorticoid receptor-like (DNA-binding domain) | 0.005392 | Inherited |
Family A G protein-coupled receptor-like | 0.005558 | Inherited |
Fibronectin type III | 0.00753 | Inherited |
Orange domain-like | 0.00832 | Inherited |
Caspase-like | 0.01072 | Inherited |
YWTD domain | 0.0132 | Inherited |
GAF domain-like | 0.01752 | Inherited |
EGF/Laminin | 0.02282 | Inherited |
Concanavalin A-like lectins/glucanases | 0.02393 | Inherited |
C2 domain (Calcium/lipid-binding domain, CaLB) | 0.02473 | Inherited |
p53-like transcription factors | 0.027 | Inherited |
SMAD MH1 domain | 0.02868 | Inherited |
Cupredoxins | 0.04282 | Inherited |
SNF-like | 0.04282 | Inherited |
Doublecortin (DC) | 0.05372 | Inherited |
HCP-like | 0.05372 | Inherited |
SH3-domain | 0.05965 | Inherited |
Metallo-dependent hydrolases | 0.06746 | Inherited |
Riboflavin synthase domain-like | 0.06746 | Inherited |
Ferredoxin reductase-like, C-terminal NADP-linked domain | 0.06746 | Inherited |
SRF-like | 0.07335 | Inherited |
GDNF receptor-like | 0.07335 | Inherited |
HMA, heavy metal-associated domain | 0.07335 | Inherited |
Growth factor receptor domain | 0.08636 | Inherited |
lambda repressor-like DNA-binding domains | 0.08697 | Inherited |
Heat shock protein 70kD (HSP70), C-terminal subdomain | 0.1066 | Inherited |
Clc chloride channel | 0.1066 | Inherited |
GTPase activation domain, GAP | 0.1177 | Inherited |
TIMP-like | 0.1295 | Inherited |
PH domain-like | 0.1546 | Inherited |
Cysteine-rich domain | 0.1666 | Inherited |
Kringle-like | 0.1679 | Inherited |
Cystine-knot cytokines | 0.1682 | Inherited |
L domain-like | 0.1702 | Inherited |
Bcl-2 inhibitors of programmed cell death | 0.1727 | Inherited |
Cap-Gly domain | 0.1749 | Inherited |
Flavoproteins | 0.1749 | Inherited |
Cadherin-like | 0.1898 | Inherited |
SNARE fusion complex | 0.1911 | Inherited |
cAMP-binding domain-like | 0.1947 | Inherited |
4-helical cytokines | 0.237 | Inherited |
Cyclin-like | 0.239 | Inherited |
Zn-dependent exopeptidases | 0.2599 | Inherited |
Immunoglobulin | 0.2599 | Inherited |
Formate/glycerate dehydrogenase catalytic domain-like | 0.2766 | Inherited |
CBS-domain pair | 0.3016 | Inherited |
Second domain of FERM | 0.3119 | Inherited |
Integrin domains | 0.4386 | Inherited |
SAM/Pointed domain | 0.4815 | Inherited |
Spermadhesin, CUB domain | 0.4875 | Inherited |
PLP-dependent transferases | 0.5056 | Inherited |
MFS general substrate transporter | 0.5266 | Inherited |
HD-domain/PDEase-like | 0.5442 | Inherited |
BAR/IMD domain-like | 0.5735 | Inherited |
HMG-box | 0.6039 | Inherited |
TNF receptor-like | 0.6055 | Inherited |
Toll/Interleukin receptor TIR domain | 0.6217 | Inherited |
Bromodomain | 0.6471 | Inherited |
PreATP-grasp domain | 0.6708 | Inherited |
Intermediate filament protein, coiled coil region | 0.7143 | Inherited |
Complement control module/SCR domain | 0.7397 | Inherited |
FAD/NAD(P)-binding domain | 0.773 | Inherited |
ABC transporter transmembrane region | 0.8399 | Inherited |
Glutathione synthetase ATP-binding domain-like | 0.8774 | Inherited |
SAP domain | 0.8903 | Inherited |
beta-beta-alpha zinc fingers | 0.9352 | Inherited |
alpha/beta-Hydrolases | 0.9748 | Inherited |
RNA-binding domain, RBD | 0.9999 | Inherited |
Cysteine proteinases | 1 | Inherited |
Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]
Family(show details)
Family domains annotated to this MP term (SDMP level: Least Informative)
Highlighted in gray are those with FDR_all>0.001
SCOP term | FDR (all) | Annotation (direct or inherited) |
Hedgehog (development protein), N-terminal signaling domain | 0 | DIRECT |
Lamin A/C globular tail domain | 0 | DIRECT |
Proton glutamate symport protein | 0 | DIRECT |
Transcriptional factor tubby, C-terminal domain | 0 | DIRECT |
Vasodilator-stimulated phosphoprotein, VASP, tetramerisation domain | 0 | DIRECT |
Notch domain | 0 | DIRECT |
Nitric oxide (NO) synthase oxygenase domain | 0 | DIRECT |
Hedgehog C-terminal (Hog) autoprocessing domain | 0 | DIRECT |
Other IPT/TIG domains | 0 | DIRECT |
Hydantoinase (dihydropyrimidinase) | 0 | DIRECT |
Synapsin C-terminal domain | 0 | DIRECT |
Neurotrophin | 0 | DIRECT |
Oligoxyloglucan reducing end-specific cellobiohydrolase | 0 | DIRECT |
Hydantoinase (dihydropyrimidinase), catalytic domain | 0 | DIRECT |
Metallothionein | 0 | DIRECT |
E2F dimerization segment | 0 | DIRECT |
Retinoblastoma tumor suppressor domains | 0 | DIRECT |
Synuclein | 0 | DIRECT |
Cytochrome p450 reductase N-terminal domain-like | 0 | DIRECT |
Synapsin domain | 0 | DIRECT |
Homeodomain | 0.000000000002318 | DIRECT |
Nicotinic receptor ligand binding domain-like | 0.0000000004052 | DIRECT |
Neurotransmitter-gated ion-channel transmembrane pore | 0.0000000004052 | DIRECT |
L-arabinose binding protein-like | 0.0000006887 | DIRECT |
Laminin G-like module | 0.000001364 | DIRECT |
Phosphate binding protein-like | 0.00000503 | DIRECT |
PDZ domain | 0.00002349 | DIRECT |
HLH, helix-loop-helix DNA-binding domain | 0.00003363 | DIRECT |
Nuclear receptor | 0.00006464 | DIRECT |
Nuclear receptor ligand-binding domain | 0.0002256 | DIRECT |
Sema domain | 0.0003228 | DIRECT |
Frizzled cysteine-rich domain | 0.0004267 | DIRECT |
Plexin repeat | 0.0005163 | DIRECT |
Spectrin repeat | 0.0007532 | DIRECT |
Laminin-type module | 0.0008421 | DIRECT |
L27 domain | 0.001299 | INHERITED FROM: abnormal excitatory postsynaptic currents |
Hypoxia-inducible factor Hif2a, C-terminal domain | 0.002294 | INHERITED FROM: abnormal forebrain morphology || abnormal brain ventricle size || enlarged brain ventricles |
DEP domain | 0.002919 | INHERITED FROM: increased neuron number || abnormal orientation of cochlear hair cell stereociliary bundles || craniorachischisis || abnormal hair cell morphology || abnormal cochlear hair cell stereociliary bundle morphology || abnormal cochlear hair cell morphology || abnormal cochlear hair cell number || increased sensory neuron number || increased cochlear hair cell number || abnormal cochlear outer hair cell morphology |
Caspase catalytic domain | 0.002919 | INHERITED FROM: abnormal neuron physiology || abnormal neuron apoptosis |
Rhodopsin-like | 0.002932 | INHERITED FROM: abnormal chemoreceptor morphology || increased susceptibility to pharmacologically induced seizures || abnormal olfactory bulb development || abnormal dopamine level || abnormal olfactory neuron innervation pattern || abnormal olfactory sensory neuron morphology || increased thyrotroph cell number |
Voltage-gated potassium channels | 0.004647 | INHERITED FROM: abnormal afterhyperpolarization || abnormal nervous system electrophysiology || abnormal channel response || abnormal olfactory bulb glomerular layer morphology || seizures || increased susceptibility to pharmacologically induced seizures || abnormal nervous system physiology |
Hairy Orange domain | 0.00639 | INHERITED FROM: increased neuron number || increased sensory neuron number |
Ephrin ectodomain | 0.00639 | INHERITED FROM: abnormal neuron morphology || abnormal thalamus morphology || reduced long term potentiation || abnormal axon morphology || abnormal CNS synaptic transmission || abnormal olfactory bulb morphology |
Fibronectin type III | 0.01017 | INHERITED FROM: abnormal axon guidance |
YWTD domain | 0.01098 | INHERITED FROM: abnormal cerebellum morphology || reduced long term potentiation || amyloid beta deposits || abnormal metencephalon morphology |
Paired domain | 0.01197 | INHERITED FROM: abnormal midbrain morphology || abnormal somatic sensory system morphology || abnormal brain ventricle morphology || abnormal brainstem morphology |
Cell cycle transcription factor e2f-dp | 0.01197 | INHERITED FROM: abnormal retinal bipolar cell morphology || decreased retinal ganglion cell number || decreased sensory neuron number || abnormal retinal ganglion cell morphology |
DIX domain | 0.01376 | INHERITED FROM: abnormal brain morphology || increased neuron number || abnormal orientation of cochlear hair cell stereociliary bundles || abnormal mechanoreceptor morphology || craniorachischisis || abnormal hair cell morphology || abnormal cochlear hair cell stereociliary bundle morphology || abnormal neural tube closure || abnormal cochlear hair cell morphology || exencephaly || abnormal cochlear hair cell number || abnormal neural tube morphology || increased sensory neuron number || abnormal nervous system development || increased cochlear hair cell number || abnormal cochlear outer hair cell morphology |
GAF domain | 0.01376 | INHERITED FROM: abnormal retinal photoreceptor morphology || decreased retinal photoreceptor cell number || decreased sensory neuron number || retinal photoreceptor degeneration || neuron degeneration |
I set domains | 0.01609 | INHERITED FROM: abnormal paranode morphology || abnormal innervation |
LDL receptor-like module | 0.02321 | INHERITED FROM: amyloid beta deposits |
SMAD MH1 domain | 0.02339 | INHERITED FROM: abnormal brain morphology || abnormal nervous system development |
SMAD domain | 0.02339 | INHERITED FROM: abnormal brain morphology || abnormal nervous system development |
NADPH-cytochrome p450 reductase-like | 0.02909 | INHERITED FROM: abnormal seizure response to inducing agent |
NADPH-cytochrome p450 reductase FAD-binding domain-like | 0.02909 | INHERITED FROM: abnormal seizure response to inducing agent |
Extracellular domain of cell surface receptors | 0.02986 | INHERITED FROM: abnormal retinal ganglion cell morphology |
Enabled/VASP homology 1 domain (EVH1 domain) | 0.02986 | INHERITED FROM: abnormal radial glial cell morphology || abnormal subarachnoid space morphology || abnormal brain ventricle morphology || absent brain internal capsule || abnormal cortical intermediate zone morphology || abnormal brain ventricle size || abnormal glial cell morphology || abnormal brain pia mater morphology || abnormal brain white matter morphology || ectopic neuron || abnormal brain ventricular system morphology || abnormal brain meninges morphology || enlarged brain ventricles || abnormal cortical plate morphology || ectopic cortical neuron || abnormal meninges morphology || abnormal CNS glial cell morphology || abnormal neurite morphology || hydroencephaly |
SNF-like | 0.03699 | INHERITED FROM: abnormal sensorimotor gating || abnormal CNS synaptic transmission |
cAMP-binding domain | 0.03745 | INHERITED FROM: abnormal olfactory bulb glomerular layer morphology || decreased retinal photoreceptor cell number |
L domain | 0.04467 | INHERITED FROM: abnormal spinal cord morphology || abnormal somatic nervous system morphology || abnormal somatic sensory system morphology || abnormal trigeminal nerve morphology || abnormal myelination || decreased neuron number || abnormal nervous system development || abnormal cerebellar layer morphology |
Doublecortin (DC) | 0.04467 | INHERITED FROM: abnormal hippocampus layer morphology || abnormal dentate gyrus morphology |
Formate/glycerate dehydrogenases, substrate-binding domain | 0.06073 | INHERITED FROM: abnormal embryonic neuroepithelium morphology || abnormal neural tube morphology |
beta-glycanases | 0.06073 | INHERITED FROM: abnormal striatum morphology || abnormal cerebellum morphology || abnormal temporal lobe morphology || abnormal telencephalon morphology || abnormal cerebral hemisphere morphology || abnormal basal ganglion morphology || abnormal hindbrain morphology || abnormal hippocampus morphology || abnormal limbic system morphology || abnormal metencephalon morphology |
GDNF receptor-like | 0.06073 | INHERITED FROM: abnormal somatic sensory system morphology || abnormal autonomic nervous system morphology |
Mib/herc2 domain | 0.06073 | INHERITED FROM: abnormal brain development |
Multidrug efflux transporter AcrB transmembrane domain | 0.06073 | INHERITED FROM: abnormal diencephalon morphology |
SRF-like | 0.06073 | INHERITED FROM: enhanced paired-pulse facilitation || decreased brain size || abnormal long term potentiation || abnormal neuron physiology || abnormal brain size || abnormal CNS synaptic transmission || abnormal paired-pulse facilitation || abnormal synaptic transmission |
HMA, heavy metal-associated domain | 0.06073 | INHERITED FROM: abnormal brain copper level |
SH3-domain | 0.07406 | INHERITED FROM: abnormal hippocampus pyramidal cell layer || short cochlear hair cell stereocilia || decreased excitatory postsynaptic current amplitude || abnormal synaptic vesicle recycling |
Pyridoxal-dependent decarboxylase | 0.08333 | INHERITED FROM: abnormal inhibitory postsynaptic currents || abnormal neurotransmitter level || abnormal synaptic transmission |
Clc chloride channel | 0.0934 | INHERITED FROM: abnormal retinal photoreceptor morphology || abnormal photoreceptor outer segment morphology || abnormal photoreceptor inner segment morphology |
Heat shock protein 70kD (HSP70), C-terminal subdomain | 0.0934 | INHERITED FROM: altered response to CNS ischemic injury |
Ephrin receptor ligand binding domain | 0.09716 | INHERITED FROM: abnormal axon guidance || decreased corpus callosum size || abnormal brain white matter morphology || abnormal axon morphology || abnormal optic tract morphology || abnormal axon pruning || abnormal innervation || abnormal nervous system tract morphology |
NF-kappa-B/REL/DORSAL transcription factors, C-terminal domain | 0.09716 | INHERITED FROM: abnormal sensory neuron innervation pattern || abnormal trigeminal nerve morphology || abnormal spinal cord dorsal column morphology |
Rel/Dorsal transcription factors, DNA-binding domain | 0.09758 | INHERITED FROM: abnormal spinal cord white matter morphology || abnormal sensory neuron innervation pattern || abnormal trigeminal nerve morphology || abnormal spinal cord dorsal column morphology |
Phosphotyrosine-binding domain (PTB) | 0.09873 | INHERITED FROM: abnormal cortical marginal zone morphology || abnormal NMDA-mediated synaptic currents || absent corpus callosum || abnormal postnatal subventricular zone morphology || abnormal rostral migratory stream morphology |
Forkhead DNA-binding domain | 0.1048 | INHERITED FROM: abnormal radial glial cell morphology || holoprosencephaly |
Ngr ectodomain-like | 0.1198 | INHERITED FROM: abnormal olfactory cortex morphology || abnormal spinal cord ventral commissure morphology || abnormal nervous system regeneration || abnormal olfactory tract morphology || abnormal spinal cord commissure morphology || abnormal spinal cord lateral column morphology |
EGF-type module | 0.1275 | INHERITED FROM: abnormal spinal cord ventral commissure morphology || abnormal olfactory tract morphology || abnormal cochlear inner hair cell number || abnormal spinal cord commissure morphology || fused dorsal root ganglion || increased cochlear inner hair cell number || abnormal spinal cord lateral column morphology || increased sensory neuron number |
EF-hand modules in multidomain proteins | 0.1343 | INHERITED FROM: abnormal somatic motor system morphology |
POU-specific domain | 0.1343 | INHERITED FROM: cochlear outer hair cell degeneration || abnormal cerebellar foliation || abnormal cerebellum lobule morphology || abnormal retinal ganglion cell morphology |
Bcl-2 inhibitors of programmed cell death | 0.1566 | INHERITED FROM: abnormal pons morphology || abnormal autonomic nervous system morphology || abnormal metencephalon morphology |
Cap-Gly domain | 0.1571 | INHERITED FROM: abnormal motor neuron morphology || abnormal spinal cord grey matter morphology |
SNARE fusion complex | 0.1808 | INHERITED FROM: enhanced paired-pulse facilitation || abnormal neurotransmitter secretion || abnormal axon extension |
Tetramerization domain of potassium channels | 0.1808 | INHERITED FROM: abnormal channel response || increased susceptibility to pharmacologically induced seizures || increased susceptibility to induction of seizure by inducing agent |
Cadherin | 0.2023 | INHERITED FROM: abnormal outer hair cell stereociliary bundle morphology || abnormal orientation of cochlear hair cell stereociliary bundles || abnormal cochlear hair cell stereociliary bundle morphology || abnormal orientation of outer hair cell stereociliary bundles || abnormal cochlear hair cell morphology || abnormal cochlear outer hair cell morphology |
Long-chain cytokines | 0.2046 | INHERITED FROM: abnormal glial cell physiology |
Motor proteins | 0.2086 | INHERITED FROM: decreased cochlear hair cell stereocilia number || decreased outer hair cell stereocilia number || short cochlear hair cell stereocilia || decreased inner hair cell stereocilia number || abnormal cochlear nerve compound action potential |
Protein kinase cysteine-rich domain (cys2, phorbol-binding domain) | 0.2157 | INHERITED FROM: reduced long term potentiation |
CBS-domain pair | 0.2174 | INHERITED FROM: abnormal retinal photoreceptor morphology || abnormal photoreceptor outer segment morphology || abnormal astrocyte morphology || increased astrocyte number || abnormal astrocyte number || abnormal photoreceptor inner segment morphology |
Calmodulin-like | 0.2186 | INHERITED FROM: abnormal retinal cone cell morphology |
Synaptotagmin-like (S variant) | 0.23 | INHERITED FROM: abnormal synaptic vesicle number || abnormal miniature endplate potential |
Fibronectin type II module | 0.2306 | INHERITED FROM: altered response to CNS ischemic injury |
Adenylyl and guanylyl cyclase catalytic domain | 0.2323 | INHERITED FROM: abnormal sensory neuron morphology |
SAM (sterile alpha motif) domain | 0.2377 | INHERITED FROM: abnormal axon guidance || decreased corpus callosum size || reduced long term depression || abnormal axon pruning || abnormal nervous system tract morphology |
Formate/glycerate dehydrogenases, NAD-domain | 0.2559 | INHERITED FROM: abnormal embryonic neuroepithelium morphology |
Leucine zipper domain | 0.2831 | INHERITED FROM: absence seizures |
Transforming growth factor (TGF)-beta | 0.2946 | INHERITED FROM: abnormal enteric neuron morphology || abnormal enteric nervous system morphology |
Acetylcholinesterase-like | 0.3111 | INHERITED FROM: abnormal synaptic bouton morphology || abnormal excitatory postsynaptic currents || abnormal synapse morphology || decreased excitatory postsynaptic current amplitude || abnormal excitatory postsynaptic current amplitude || abnormal inhibitory postsynaptic currents || abnormal miniature inhibitory postsynaptic currents || abnormal central pattern generator function || abnormal pre-Botzinger complex physiology || abnormal autonomic nervous system physiology |
PLC-like (P variant) | 0.3141 | INHERITED FROM: abnormal synaptic vesicle number |
FYVE, a phosphatidylinositol-3-phosphate binding domain | 0.3627 | INHERITED FROM: abnormal spinal cord morphology |
Histone H3 K4-specific methyltransferase SET7/9 N-terminal domain | 0.3666 | INHERITED FROM: abnormal nervous system electrophysiology |
Cyclin | 0.3739 | INHERITED FROM: ectopic Purkinje cell || small cerebellum || abnormal cerebellar foliation || absent Purkinje cell layer || abnormal cerebellum lobule morphology |
Cytoplasmic domain of inward rectifier potassium channel | 0.3941 | INHERITED FROM: tonic-clonic seizures |
Growth factor receptor domain | 0.3946 | INHERITED FROM: abnormal cochlear inner hair cell number || abnormal cochlear hair cell morphology || abnormal nervous system development || abnormal cochlear outer hair cell morphology |
PDEase | 0.4046 | INHERITED FROM: decreased retinal photoreceptor cell number || retinal photoreceptor degeneration |
p120GAP domain-like | 0.4307 | INHERITED FROM: abnormal dendrite morphology |
Integrin domains | 0.4365 | INHERITED FROM: abnormal sciatic nerve morphology |
Actin/HSP70 | 0.4384 | INHERITED FROM: altered response to CNS ischemic injury |
C1 set domains (antibody constant domain-like) | 0.4384 | INHERITED FROM: enhanced paired-pulse facilitation |
Integrin alpha N-terminal domain | 0.4384 | INHERITED FROM: axon degeneration |
Spermadhesin, CUB domain | 0.4969 | INHERITED FROM: short excitatory postsynaptic current rise time || abnormal excitatory postsynaptic currents || biphasic excitatory postsynaptic current amplitude || decreased excitatory postsynaptic current amplitude || abnormal Purkinje cell innervation |
TNF receptor-like | 0.5111 | INHERITED FROM: abnormal nervous system regeneration || altered response to CNS ischemic injury || abnormal myelination |
HMG-box | 0.6139 | INHERITED FROM: abnormal sympathetic neuron morphology || optic nerve hypoplasia || abnormal sympathetic ganglion morphology || abnormal paravertebral ganglion morphology || abnormal superior cervical ganglion morphology |
Bromodomain | 0.6504 | INHERITED FROM: abnormal neural tube closure |
G proteins | 0.6882 | INHERITED FROM: abnormal neurotransmitter secretion |
Toll/Interleukin receptor TIR domain | 0.7126 | INHERITED FROM: abnormal glial cell physiology || decreased neuron apoptosis |
Intermediate filament protein, coiled coil region | 0.7235 | INHERITED FROM: abnormal axonal transport || abnormal spinal nerve morphology |
Complement control module/SCR domain | 0.7462 | INHERITED FROM: short excitatory postsynaptic current rise time || biphasic excitatory postsynaptic current amplitude || decreased excitatory postsynaptic current amplitude || abnormal Purkinje cell innervation |
BAR domain | 0.7468 | INHERITED FROM: abnormal synaptic vesicle number || decreased excitatory postsynaptic current amplitude || abnormal synaptic vesicle recycling || abnormal excitatory postsynaptic current amplitude || abnormal synaptic vesicle morphology || increased synaptic depression |
ABC transporter transmembrane region | 0.8399 | INHERITED FROM: amyloid beta deposits || nervous system inclusion bodies |
MAM domain | 0.8859 | INHERITED FROM: abnormal neuronal migration |
SAP domain | 0.8859 | INHERITED FROM: abnormal striatum morphology || abnormal basal ganglion morphology |
Classic zinc finger, C2H2 | 0.9004 | INHERITED FROM: abnormal olfactory nerve morphology || abnormal brain development |
SH2 domain | 0.9022 | INHERITED FROM: abnormal central pattern generator function |
ABC transporter ATPase domain-like | 0.9153 | INHERITED FROM: nervous system inclusion bodies |
Canonical RBD | 0.9695 | INHERITED FROM: premature neuronal precursor differentiation |
V set domains (antibody variable domain-like) | 1 | INHERITED FROM: brain inflammation || abnormal myelination || CNS inflammation || demyelination |
SCOP term | FDR (all) | Annotation (direct or inherited) |
Hedgehog (development protein), N-terminal signaling domain | 0 | Direct |
Lamin A/C globular tail domain | 0 | Direct |
Proton glutamate symport protein | 0 | Direct |
Transcriptional factor tubby, C-terminal domain | 0 | Direct |
Vasodilator-stimulated phosphoprotein, VASP, tetramerisation domain | 0 | Direct |
Notch domain | 0 | Direct |
Nitric oxide (NO) synthase oxygenase domain | 0 | Direct |
Hedgehog C-terminal (Hog) autoprocessing domain | 0 | Direct |
Other IPT/TIG domains | 0 | Direct |
Hydantoinase (dihydropyrimidinase) | 0 | Direct |
Synapsin C-terminal domain | 0 | Direct |
Neurotrophin | 0 | Direct |
Oligoxyloglucan reducing end-specific cellobiohydrolase | 0 | Direct |
Hydantoinase (dihydropyrimidinase), catalytic domain | 0 | Direct |
Metallothionein | 0 | Direct |
E2F dimerization segment | 0 | Direct |
Retinoblastoma tumor suppressor domains | 0 | Direct |
Synuclein | 0 | Direct |
Cytochrome p450 reductase N-terminal domain-like | 0 | Direct |
Synapsin domain | 0 | Direct |
Homeodomain | 0.000000000002318 | Direct |
Nicotinic receptor ligand binding domain-like | 0.0000000004052 | Direct |
Neurotransmitter-gated ion-channel transmembrane pore | 0.0000000004052 | Direct |
L-arabinose binding protein-like | 0.0000006887 | Direct |
Laminin G-like module | 0.000001364 | Direct |
Phosphate binding protein-like | 0.00000503 | Direct |
PDZ domain | 0.00002349 | Direct |
HLH, helix-loop-helix DNA-binding domain | 0.00003363 | Direct |
Nuclear receptor | 0.00006464 | Direct |
Nuclear receptor ligand-binding domain | 0.0002256 | Direct |
Sema domain | 0.0003228 | Direct |
Frizzled cysteine-rich domain | 0.0004267 | Direct |
Plexin repeat | 0.0005163 | Direct |
Spectrin repeat | 0.0007532 | Direct |
Laminin-type module | 0.0008421 | Direct |
L27 domain | 0.001299 | Inherited |
Hypoxia-inducible factor Hif2a, C-terminal domain | 0.002294 | Inherited |
DEP domain | 0.002919 | Inherited |
Caspase catalytic domain | 0.002919 | Inherited |
Rhodopsin-like | 0.002932 | Inherited |
Voltage-gated potassium channels | 0.004647 | Inherited |
Hairy Orange domain | 0.00639 | Inherited |
Ephrin ectodomain | 0.00639 | Inherited |
Fibronectin type III | 0.01017 | Inherited |
YWTD domain | 0.01098 | Inherited |
Paired domain | 0.01197 | Inherited |
Cell cycle transcription factor e2f-dp | 0.01197 | Inherited |
DIX domain | 0.01376 | Inherited |
GAF domain | 0.01376 | Inherited |
I set domains | 0.01609 | Inherited |
LDL receptor-like module | 0.02321 | Inherited |
SMAD MH1 domain | 0.02339 | Inherited |
SMAD domain | 0.02339 | Inherited |
NADPH-cytochrome p450 reductase-like | 0.02909 | Inherited |
NADPH-cytochrome p450 reductase FAD-binding domain-like | 0.02909 | Inherited |
Extracellular domain of cell surface receptors | 0.02986 | Inherited |
Enabled/VASP homology 1 domain (EVH1 domain) | 0.02986 | Inherited |
SNF-like | 0.03699 | Inherited |
cAMP-binding domain | 0.03745 | Inherited |
L domain | 0.04467 | Inherited |
Doublecortin (DC) | 0.04467 | Inherited |
Formate/glycerate dehydrogenases, substrate-binding domain | 0.06073 | Inherited |
beta-glycanases | 0.06073 | Inherited |
GDNF receptor-like | 0.06073 | Inherited |
Mib/herc2 domain | 0.06073 | Inherited |
Multidrug efflux transporter AcrB transmembrane domain | 0.06073 | Inherited |
SRF-like | 0.06073 | Inherited |
HMA, heavy metal-associated domain | 0.06073 | Inherited |
SH3-domain | 0.07406 | Inherited |
Pyridoxal-dependent decarboxylase | 0.08333 | Inherited |
Clc chloride channel | 0.0934 | Inherited |
Heat shock protein 70kD (HSP70), C-terminal subdomain | 0.0934 | Inherited |
Ephrin receptor ligand binding domain | 0.09716 | Inherited |
NF-kappa-B/REL/DORSAL transcription factors, C-terminal domain | 0.09716 | Inherited |
Rel/Dorsal transcription factors, DNA-binding domain | 0.09758 | Inherited |
Phosphotyrosine-binding domain (PTB) | 0.09873 | Inherited |
Forkhead DNA-binding domain | 0.1048 | Inherited |
Ngr ectodomain-like | 0.1198 | Inherited |
EGF-type module | 0.1275 | Inherited |
EF-hand modules in multidomain proteins | 0.1343 | Inherited |
POU-specific domain | 0.1343 | Inherited |
Bcl-2 inhibitors of programmed cell death | 0.1566 | Inherited |
Cap-Gly domain | 0.1571 | Inherited |
SNARE fusion complex | 0.1808 | Inherited |
Tetramerization domain of potassium channels | 0.1808 | Inherited |
Cadherin | 0.2023 | Inherited |
Long-chain cytokines | 0.2046 | Inherited |
Motor proteins | 0.2086 | Inherited |
Protein kinase cysteine-rich domain (cys2, phorbol-binding domain) | 0.2157 | Inherited |
CBS-domain pair | 0.2174 | Inherited |
Calmodulin-like | 0.2186 | Inherited |
Synaptotagmin-like (S variant) | 0.23 | Inherited |
Fibronectin type II module | 0.2306 | Inherited |
Adenylyl and guanylyl cyclase catalytic domain | 0.2323 | Inherited |
SAM (sterile alpha motif) domain | 0.2377 | Inherited |
Formate/glycerate dehydrogenases, NAD-domain | 0.2559 | Inherited |
Leucine zipper domain | 0.2831 | Inherited |
Transforming growth factor (TGF)-beta | 0.2946 | Inherited |
Acetylcholinesterase-like | 0.3111 | Inherited |
PLC-like (P variant) | 0.3141 | Inherited |
FYVE, a phosphatidylinositol-3-phosphate binding domain | 0.3627 | Inherited |
Histone H3 K4-specific methyltransferase SET7/9 N-terminal domain | 0.3666 | Inherited |
Cyclin | 0.3739 | Inherited |
Cytoplasmic domain of inward rectifier potassium channel | 0.3941 | Inherited |
Growth factor receptor domain | 0.3946 | Inherited |
PDEase | 0.4046 | Inherited |
p120GAP domain-like | 0.4307 | Inherited |
Integrin domains | 0.4365 | Inherited |
Actin/HSP70 | 0.4384 | Inherited |
C1 set domains (antibody constant domain-like) | 0.4384 | Inherited |
Integrin alpha N-terminal domain | 0.4384 | Inherited |
Spermadhesin, CUB domain | 0.4969 | Inherited |
TNF receptor-like | 0.5111 | Inherited |
HMG-box | 0.6139 | Inherited |
Bromodomain | 0.6504 | Inherited |
G proteins | 0.6882 | Inherited |
Toll/Interleukin receptor TIR domain | 0.7126 | Inherited |
Intermediate filament protein, coiled coil region | 0.7235 | Inherited |
Complement control module/SCR domain | 0.7462 | Inherited |
BAR domain | 0.7468 | Inherited |
ABC transporter transmembrane region | 0.8399 | Inherited |
MAM domain | 0.8859 | Inherited |
SAP domain | 0.8859 | Inherited |
Classic zinc finger, C2H2 | 0.9004 | Inherited |
SH2 domain | 0.9022 | Inherited |
ABC transporter ATPase domain-like | 0.9153 | Inherited |
Canonical RBD | 0.9695 | Inherited |
V set domains (antibody variable domain-like) | 1 | Inherited |
Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]
Supra-domain (including individual superfamily)
(show details)
Supra-domains annotated to this MP term (Not in SPMP)
Highlighted in gray are those with FDR>0.001
Supra-domain (Single) |
FDR (all) |
Annotation (direct or inherited) |
Tubby C-terminal domain-like | 0 | DIRECT |
Nitric oxide (NO) synthase oxygenase domain | 0 | DIRECT |
Synuclein | 0 | DIRECT |
Hedgehog/intein (Hint) domain | 0 | DIRECT |
Metallothionein | 0 | DIRECT |
Vasodilator-stimulated phosphoprotein, VASP, tetramerisation domain | 0 | DIRECT |
Oligoxyloglucan reducing end-specific cellobiohydrolase | 0 | DIRECT |
Proton glutamate symport protein | 0 | DIRECT |
Notch domain | 0 | DIRECT |
Hedgehog/DD-peptidase | 0 | DIRECT |
Lamin A/C globular tail domain | 0 | DIRECT |
Composite domain of metallo-dependent hydrolases | 0 | DIRECT |
E2F-DP heterodimerization region | 0 | DIRECT |
Homeodomain-like | 0.0000000000003159 | DIRECT |
Neurotransmitter-gated ion-channel transmembrane pore | 0.0000000001318 | DIRECT |
Nicotinic receptor ligand binding domain-like | 0.0000000001318 | DIRECT |
Periplasmic binding protein-like I | 0.00000001092 | DIRECT |
PDZ domain-like | 0.000001447 | DIRECT |
HLH, helix-loop-helix DNA-binding domain | 0.0000111 | DIRECT |
Voltage-gated potassium channels | 0.00001802 | DIRECT |
Spectrin repeat | 0.00006149 | DIRECT |
Periplasmic binding protein-like II | 0.00006205 | DIRECT |
Nuclear receptor ligand-binding domain | 0.0001155 | DIRECT |
NHL repeat | 0.000177 | DIRECT |
Sema domain | 0.0001913 | DIRECT |
Frizzled cysteine-rich domain | 0.0002799 | DIRECT |
Plexin repeat | 0.0002967 | DIRECT |
Galactose-binding domain-like | 0.0008855 | DIRECT |
L27 domain | 0.0009832 | DIRECT |
Glucocorticoid receptor-like (DNA-binding domain) | 0.00324 | INHERITED FROM: abnormal Rathke's pouch development || absent choroid plexus || abnormal optic disc morphology || abnormal cranial nerve morphology || decreased gonadotroph cell number |
Family A G protein-coupled receptor-like | 0.003344 | INHERITED FROM: abnormal olfactory bulb development || abnormal dopamine level || abnormal olfactory neuron innervation pattern || increased thyrotroph cell number || abnormal chemoreceptor morphology || abnormal olfactory sensory neuron morphology |
Fibronectin type III | 0.004617 | INHERITED FROM: abnormal axon guidance |
Orange domain-like | 0.005136 | INHERITED FROM: increased neuron number || increased sensory neuron number |
Caspase-like | 0.00673 | INHERITED FROM: abnormal neuron apoptosis || abnormal neuron physiology |
YWTD domain | 0.008399 | INHERITED FROM: abnormal metencephalon morphology || abnormal cerebellum morphology || reduced long term potentiation || amyloid beta deposits || nervous system inclusion bodies |
GAF domain-like | 0.0114 | INHERITED FROM: retinal photoreceptor degeneration || decreased retinal photoreceptor cell number || neuron degeneration || decreased neuron number || abnormal retinal photoreceptor morphology || decreased sensory neuron number |
EGF/Laminin | 0.01513 | INHERITED FROM: decreased cerebral infarction size || abnormal rostral migratory stream morphology || abnormal Schwann cell morphology || abnormal spinal cord white matter morphology || abnormal spinal cord commissure morphology || abnormal spinal cord ventral commissure morphology || abnormal orientation of cochlear hair cell stereociliary bundles || abnormal cochlear inner hair cell number || increased cochlear inner hair cell number || fused dorsal root ganglion |
Concanavalin A-like lectins/glucanases | 0.01593 | INHERITED FROM: abnormal NMDA-mediated synaptic currents || abnormal spinal cord commissure morphology || abnormal paired-pulse inhibition || abnormal spinal cord ventral commissure morphology || decreased CNS synapse formation || reduced AMPA-mediated synaptic currents |
C2 domain (Calcium/lipid-binding domain, CaLB) | 0.01651 | INHERITED FROM: abnormal synaptic vesicle number || abnormal synaptic vesicle morphology |
LDL receptor-like module | 0.01653 | INHERITED FROM: amyloid beta deposits |
p53-like transcription factors | 0.01815 | INHERITED FROM: abnormal spinal cord dorsal column morphology |
SMAD MH1 domain | 0.0194 | INHERITED FROM: abnormal brain morphology || abnormal nervous system development |
SNF-like | 0.02989 | INHERITED FROM: abnormal CNS synaptic transmission || abnormal sensorimotor gating |
Cupredoxins | 0.02989 | INHERITED FROM: reduced long term potentiation || abnormal thalamus morphology |
Doublecortin (DC) | 0.03817 | INHERITED FROM: abnormal hippocampus layer morphology || abnormal temporal lobe morphology || abnormal dentate gyrus morphology || abnormal hippocampus morphology |
HCP-like | 0.03817 | INHERITED FROM: abnormal neural tube morphology |
E set domains | 0.04255 | INHERITED FROM: abnormal hippocampal mossy fiber morphology |
SH3-domain | 0.04292 | INHERITED FROM: short cochlear hair cell stereocilia || decreased excitatory postsynaptic current amplitude || abnormal hippocampus pyramidal cell layer || abnormal synaptic vesicle recycling |
Metallo-dependent hydrolases | 0.04914 | INHERITED FROM: abnormal dendrite morphology || abnormal hippocampus pyramidal cell morphology || abnormal hippocampus layer morphology || abnormal hippocampus pyramidal cell layer |
Riboflavin synthase domain-like | 0.04914 | INHERITED FROM: decreased cerebral infarction size || abnormal seizure response to inducing agent || reduced long term potentiation || altered response to CNS ischemic injury || decreased susceptibility to ischemic brain injury || abnormal blood-brain barrier function |
Ferredoxin reductase-like, C-terminal NADP-linked domain | 0.04914 | INHERITED FROM: decreased cerebral infarction size || abnormal seizure response to inducing agent || reduced long term potentiation || altered response to CNS ischemic injury || decreased susceptibility to ischemic brain injury || abnormal blood-brain barrier function |
SRF-like | 0.05384 | INHERITED FROM: abnormal long term potentiation || abnormal paired-pulse facilitation || abnormal CNS synaptic transmission || abnormal neuron physiology || abnormal synaptic transmission || abnormal brain size || enhanced paired-pulse facilitation || decreased brain size |
HMA, heavy metal-associated domain | 0.05384 | INHERITED FROM: abnormal brain copper level |
GDNF receptor-like | 0.05384 | INHERITED FROM: abnormal autonomic nervous system morphology || abnormal somatic sensory system morphology |
Mib/herc2 domain-like | 0.05384 | INHERITED FROM: abnormal brain development |
Growth factor receptor domain | 0.06426 | INHERITED FROM: abnormal rostral migratory stream morphology || decreased Schwann cell number || abnormal cochlear inner hair cell number || abnormal nervous system development |
lambda repressor-like DNA-binding domains | 0.06474 | INHERITED FROM: abnormal embryonic/fetal subventricular zone morphology || cochlear outer hair cell degeneration || abnormal neocortex morphology |
Glutamine synthetase/guanido kinase | 0.07313 | INHERITED FROM: abnormal limbic system morphology |
Multidrug efflux transporter AcrB transmembrane domain | 0.08107 | INHERITED FROM: abnormal diencephalon morphology |
Heat shock protein 70kD (HSP70), C-terminal subdomain | 0.08107 | INHERITED FROM: altered response to CNS ischemic injury |
Clc chloride channel | 0.08107 | INHERITED FROM: abnormal photoreceptor inner segment morphology || abnormal photoreceptor outer segment morphology || abnormal retinal photoreceptor morphology |
GTPase activation domain, GAP | 0.09063 | INHERITED FROM: abnormal cerebellar granule cell morphology || abnormal astrocyte physiology || ectopic cerebellar granule cells || abnormal cerebral hemisphere morphology |
TIMP-like | 0.1007 | INHERITED FROM: spina bifida || craniorachischisis || amyloid beta deposits |
PH domain-like | 0.1229 | INHERITED FROM: abnormal brain pia mater morphology || abnormal meninges morphology |
Cysteine-rich domain | 0.1332 | INHERITED FROM: reduced long term potentiation |
Kringle-like | 0.1343 | INHERITED FROM: altered response to CNS ischemic injury |
Cystine-knot cytokines | 0.1345 | INHERITED FROM: abnormal paravertebral ganglion morphology || abnormal autonomic nervous system morphology || abnormal petrosal ganglion morphology || small geniculate ganglion || abnormal superior cervical ganglion morphology || small petrosal ganglion || abnormal L4 dorsal root ganglion morphology || small nodose ganglion || small trigeminal ganglion |
L domain-like | 0.1363 | INHERITED FROM: abnormal spinal cord lateral column morphology || abnormal petrosal ganglion morphology || abnormal spinal cord ventral commissure morphology || abnormal nervous system regeneration || abnormal sensory neuron innervation pattern || abnormal olfactory tract morphology |
Bcl-2 inhibitors of programmed cell death | 0.1386 | INHERITED FROM: abnormal metencephalon morphology || abnormal autonomic nervous system morphology || abnormal pons morphology |
Cap-Gly domain | 0.1405 | INHERITED FROM: abnormal spinal cord grey matter morphology || abnormal motor neuron morphology |
Flavoproteins | 0.1405 | INHERITED FROM: abnormal seizure response to inducing agent |
Cadherin-like | 0.1541 | INHERITED FROM: abnormal orientation of outer hair cell stereociliary bundles || abnormal cochlear outer hair cell morphology || abnormal outer hair cell stereociliary bundle morphology || abnormal orientation of cochlear hair cell stereociliary bundles || abnormal cochlear hair cell stereociliary bundle morphology |
SNARE fusion complex | 0.1553 | INHERITED FROM: abnormal neurotransmitter secretion || abnormal axon extension || enhanced paired-pulse facilitation |
cAMP-binding domain-like | 0.1585 | INHERITED FROM: abnormal olfactory bulb glomerular layer morphology |
BRCT domain | 0.1727 | INHERITED FROM: decreased brain size |
4-helical cytokines | 0.1976 | INHERITED FROM: increased pituitary adenoma incidence || increased pituitary gland tumor incidence || increased nervous system tumor incidence || CNS inflammation || abnormal glial cell physiology |
Cyclin-like | 0.1995 | INHERITED FROM: abnormal cerebellar layer morphology || abnormal cerebellar Purkinje cell layer || absent Purkinje cell layer || abnormal cerebellar cortex morphology || decreased retinal photoreceptor cell number || decreased retinal ganglion cell number || ectopic Purkinje cell || ectopic neuron || small cerebellum |
Nucleotide cyclase | 0.2021 | INHERITED FROM: abnormal sensory neuron morphology |
Zn-dependent exopeptidases | 0.2189 | INHERITED FROM: decreased prepulse inhibition || abnormal prepulse inhibition || abnormal astrocyte number |
Immunoglobulin | 0.2189 | INHERITED FROM: abnormal innervation |
Leucine zipper domain | 0.2332 | INHERITED FROM: decreased neuron apoptosis || absence seizures |
Formate/glycerate dehydrogenase catalytic domain-like | 0.2347 | INHERITED FROM: abnormal embryonic neuroepithelium morphology |
CBS-domain pair | 0.2583 | INHERITED FROM: abnormal photoreceptor inner segment morphology || abnormal photoreceptor outer segment morphology || increased astrocyte number || abnormal astrocyte number || abnormal retinal photoreceptor morphology |
Second domain of FERM | 0.2681 | INHERITED FROM: short cochlear hair cell stereocilia || abnormal outer hair cell stereociliary bundle morphology || abnormal inner hair cell stereociliary bundle morphology |
"Winged helix" DNA-binding domain | 0.303 | INHERITED FROM: increased sensory neuron number |
ARM repeat | 0.3241 | INHERITED FROM: astrocytosis |
Quinoprotein alcohol dehydrogenase-like | 0.3289 | INHERITED FROM: abnormal brain ventricle size || enlarged brain ventricles |
Histone H3 K4-specific methyltransferase SET7/9 N-terminal domain | 0.3399 | INHERITED FROM: abnormal nervous system electrophysiology |
Integrin domains | 0.3911 | INHERITED FROM: abnormal sciatic nerve morphology |
TPR-like | 0.4027 | INHERITED FROM: abnormal neuron specification |
Integrin alpha N-terminal domain | 0.4232 | INHERITED FROM: axon degeneration |
SAM/Pointed domain | 0.4338 | INHERITED FROM: abnormal axon pruning |
Spermadhesin, CUB domain | 0.4399 | INHERITED FROM: short excitatory postsynaptic current rise time || biphasic excitatory postsynaptic current amplitude || abnormal Purkinje cell innervation || decreased excitatory postsynaptic current amplitude || abnormal excitatory postsynaptic currents |
PLP-dependent transferases | 0.458 | INHERITED FROM: abnormal inhibitory postsynaptic currents || abnormal neurotransmitter level |
MFS general substrate transporter | 0.4793 | INHERITED FROM: abnormal neurotransmitter uptake |
HD-domain/PDEase-like | 0.4974 | INHERITED FROM: retinal photoreceptor degeneration || decreased retinal photoreceptor cell number |
BAR/IMD domain-like | 0.5271 | INHERITED FROM: abnormal synaptic vesicle number || abnormal excitatory postsynaptic current amplitude || decreased excitatory postsynaptic current amplitude || abnormal synaptic vesicle recycling |
HMG-box | 0.5583 | INHERITED FROM: abnormal paravertebral ganglion morphology || abnormal sympathetic ganglion morphology || abnormal superior cervical ganglion morphology || optic nerve hypoplasia || abnormal sympathetic neuron morphology |
TNF receptor-like | 0.5601 | INHERITED FROM: altered response to CNS ischemic injury || abnormal nervous system regeneration |
Toll/Interleukin receptor TIR domain | 0.5768 | INHERITED FROM: abnormal glial cell physiology |
Bromodomain | 0.6036 | INHERITED FROM: abnormal neural tube closure |
PreATP-grasp domain | 0.6285 | INHERITED FROM: abnormal synaptic depression || convulsive seizures || abnormal seizure response to inducing agent || tonic-clonic seizures || environmentally induced seizures || abnormal brain wave pattern || increased synaptic depression |
Intermediate filament protein, coiled coil region | 0.6744 | INHERITED FROM: abnormal spinal nerve morphology || abnormal axonal transport |
Complement control module/SCR domain | 0.7011 | INHERITED FROM: short excitatory postsynaptic current rise time || biphasic excitatory postsynaptic current amplitude || abnormal Purkinje cell innervation || decreased excitatory postsynaptic current amplitude |
FAD/NAD(P)-binding domain | 0.736 | INHERITED FROM: increased dopamine level |
ABC transporter transmembrane region | 0.808 | INHERITED FROM: amyloid beta deposits || nervous system inclusion bodies |
Glutathione synthetase ATP-binding domain-like | 0.8486 | INHERITED FROM: tonic-clonic seizures || environmentally induced seizures || abnormal brain wave pattern || increased synaptic depression |
SH2 domain | 0.8523 | INHERITED FROM: abnormal spinal cord dorsal column morphology || abnormal central pattern generator function |
SAP domain | 0.8626 | INHERITED FROM: abnormal striatum morphology || abnormal basal ganglion morphology |
beta-beta-alpha zinc fingers | 0.9119 | INHERITED FROM: abnormal olfactory nerve morphology |
alpha/beta-Hydrolases | 0.9567 | INHERITED FROM: decreased excitatory postsynaptic current amplitude || abnormal pre-Botzinger complex physiology || abnormal synaptic bouton morphology || abnormal autonomic nervous system physiology || abnormal central pattern generator function |
RNA-binding domain, RBD | 0.987 | INHERITED FROM: premature neuronal precursor differentiation |
Cysteine proteinases | 1 | INHERITED FROM: axonal dystrophy |
Supra-domain (Single) |
FDR (all) |
Annotation (direct or inherited) |
Tubby C-terminal domain-like | 0 | Direct |
Nitric oxide (NO) synthase oxygenase domain | 0 | Direct |
Synuclein | 0 | Direct |
Hedgehog/intein (Hint) domain | 0 | Direct |
Metallothionein | 0 | Direct |
Vasodilator-stimulated phosphoprotein, VASP, tetramerisation domain | 0 | Direct |
Oligoxyloglucan reducing end-specific cellobiohydrolase | 0 | Direct |
Proton glutamate symport protein | 0 | Direct |
Notch domain | 0 | Direct |
Hedgehog/DD-peptidase | 0 | Direct |
Lamin A/C globular tail domain | 0 | Direct |
Composite domain of metallo-dependent hydrolases | 0 | Direct |
E2F-DP heterodimerization region | 0 | Direct |
Homeodomain-like | 0.0000000000003159 | Direct |
Neurotransmitter-gated ion-channel transmembrane pore | 0.0000000001318 | Direct |
Nicotinic receptor ligand binding domain-like | 0.0000000001318 | Direct |
Periplasmic binding protein-like I | 0.00000001092 | Direct |
PDZ domain-like | 0.000001447 | Direct |
HLH, helix-loop-helix DNA-binding domain | 0.0000111 | Direct |
Voltage-gated potassium channels | 0.00001802 | Direct |
Spectrin repeat | 0.00006149 | Direct |
Periplasmic binding protein-like II | 0.00006205 | Direct |
Nuclear receptor ligand-binding domain | 0.0001155 | Direct |
NHL repeat | 0.000177 | Direct |
Sema domain | 0.0001913 | Direct |
Frizzled cysteine-rich domain | 0.0002799 | Direct |
Plexin repeat | 0.0002967 | Direct |
Galactose-binding domain-like | 0.0008855 | Direct |
L27 domain | 0.0009832 | Direct |
Glucocorticoid receptor-like (DNA-binding domain) | 0.00324 | Inherited |
Family A G protein-coupled receptor-like | 0.003344 | Inherited |
Fibronectin type III | 0.004617 | Inherited |
Orange domain-like | 0.005136 | Inherited |
Caspase-like | 0.00673 | Inherited |
YWTD domain | 0.008399 | Inherited |
GAF domain-like | 0.0114 | Inherited |
EGF/Laminin | 0.01513 | Inherited |
Concanavalin A-like lectins/glucanases | 0.01593 | Inherited |
C2 domain (Calcium/lipid-binding domain, CaLB) | 0.01651 | Inherited |
LDL receptor-like module | 0.01653 | Inherited |
p53-like transcription factors | 0.01815 | Inherited |
SMAD MH1 domain | 0.0194 | Inherited |
SNF-like | 0.02989 | Inherited |
Cupredoxins | 0.02989 | Inherited |
Doublecortin (DC) | 0.03817 | Inherited |
HCP-like | 0.03817 | Inherited |
E set domains | 0.04255 | Inherited |
SH3-domain | 0.04292 | Inherited |
Metallo-dependent hydrolases | 0.04914 | Inherited |
Riboflavin synthase domain-like | 0.04914 | Inherited |
Ferredoxin reductase-like, C-terminal NADP-linked domain | 0.04914 | Inherited |
SRF-like | 0.05384 | Inherited |
HMA, heavy metal-associated domain | 0.05384 | Inherited |
GDNF receptor-like | 0.05384 | Inherited |
Mib/herc2 domain-like | 0.05384 | Inherited |
Growth factor receptor domain | 0.06426 | Inherited |
lambda repressor-like DNA-binding domains | 0.06474 | Inherited |
Glutamine synthetase/guanido kinase | 0.07313 | Inherited |
Multidrug efflux transporter AcrB transmembrane domain | 0.08107 | Inherited |
Heat shock protein 70kD (HSP70), C-terminal subdomain | 0.08107 | Inherited |
Clc chloride channel | 0.08107 | Inherited |
GTPase activation domain, GAP | 0.09063 | Inherited |
TIMP-like | 0.1007 | Inherited |
PH domain-like | 0.1229 | Inherited |
Cysteine-rich domain | 0.1332 | Inherited |
Kringle-like | 0.1343 | Inherited |
Cystine-knot cytokines | 0.1345 | Inherited |
L domain-like | 0.1363 | Inherited |
Bcl-2 inhibitors of programmed cell death | 0.1386 | Inherited |
Cap-Gly domain | 0.1405 | Inherited |
Flavoproteins | 0.1405 | Inherited |
Cadherin-like | 0.1541 | Inherited |
SNARE fusion complex | 0.1553 | Inherited |
cAMP-binding domain-like | 0.1585 | Inherited |
BRCT domain | 0.1727 | Inherited |
4-helical cytokines | 0.1976 | Inherited |
Cyclin-like | 0.1995 | Inherited |
Nucleotide cyclase | 0.2021 | Inherited |
Zn-dependent exopeptidases | 0.2189 | Inherited |
Immunoglobulin | 0.2189 | Inherited |
Leucine zipper domain | 0.2332 | Inherited |
Formate/glycerate dehydrogenase catalytic domain-like | 0.2347 | Inherited |
CBS-domain pair | 0.2583 | Inherited |
Second domain of FERM | 0.2681 | Inherited |
"Winged helix" DNA-binding domain | 0.303 | Inherited |
ARM repeat | 0.3241 | Inherited |
Quinoprotein alcohol dehydrogenase-like | 0.3289 | Inherited |
Histone H3 K4-specific methyltransferase SET7/9 N-terminal domain | 0.3399 | Inherited |
Integrin domains | 0.3911 | Inherited |
TPR-like | 0.4027 | Inherited |
Integrin alpha N-terminal domain | 0.4232 | Inherited |
SAM/Pointed domain | 0.4338 | Inherited |
Spermadhesin, CUB domain | 0.4399 | Inherited |
PLP-dependent transferases | 0.458 | Inherited |
MFS general substrate transporter | 0.4793 | Inherited |
HD-domain/PDEase-like | 0.4974 | Inherited |
BAR/IMD domain-like | 0.5271 | Inherited |
HMG-box | 0.5583 | Inherited |
TNF receptor-like | 0.5601 | Inherited |
Toll/Interleukin receptor TIR domain | 0.5768 | Inherited |
Bromodomain | 0.6036 | Inherited |
PreATP-grasp domain | 0.6285 | Inherited |
Intermediate filament protein, coiled coil region | 0.6744 | Inherited |
Complement control module/SCR domain | 0.7011 | Inherited |
FAD/NAD(P)-binding domain | 0.736 | Inherited |
ABC transporter transmembrane region | 0.808 | Inherited |
Glutathione synthetase ATP-binding domain-like | 0.8486 | Inherited |
SH2 domain | 0.8523 | Inherited |
SAP domain | 0.8626 | Inherited |
beta-beta-alpha zinc fingers | 0.9119 | Inherited |
alpha/beta-Hydrolases | 0.9567 | Inherited |
RNA-binding domain, RBD | 0.987 | Inherited |
Cysteine proteinases | 1 | Inherited |
(show details)
Supra-domains annotated to this MP term (Not in SPMP)
Highlighted in gray are those with FDR>0.001
Supra-domain (Duplex) in N- to C-terminal order |
FDR (all) |
Annotation (direct or inherited) |
55166,51294 55166 - Hedgehog/DD-peptidase 51294 - Hedgehog/intein (Hint) domain | 0 | DIRECT |
57196,90193 57196 - EGF/Laminin 90193 - Notch domain | 0 | DIRECT |
57184,49899 57184 - Growth factor receptor domain 49899 - Concanavalin A-like lectins/glucanases | 0 | DIRECT |
90193,90193 90193 - Notch domain 90193 - Notch domain | 0 | DIRECT |
46785,144074 46785 - "Winged helix" DNA-binding domain 144074 - E2F-DP heterodimerization region | 0 | DIRECT |
50044,50156 50044 - SH3-domain 50156 - PDZ domain-like | 0 | DIRECT |
51556,51338 51556 - Metallo-dependent hydrolases 51338 - Composite domain of metallo-dependent hydrolases | 0 | DIRECT |
57196,56496 57196 - EGF/Laminin 56496 - Fibrinogen C-terminal domain-like | 0 | DIRECT |
57196,57424 57196 - EGF/Laminin 57424 - LDL receptor-like module | 0 | DIRECT |
51338,51556 51338 - Composite domain of metallo-dependent hydrolases 51556 - Metallo-dependent hydrolases | 0 | DIRECT |
81296,101898 81296 - E set domains 101898 - NHL repeat | 0 | DIRECT |
50729,57889 50729 - PH domain-like 57889 - Cysteine-rich domain | 0 | DIRECT |
64593,74853 64593 - Intermediate filament protein, coiled coil region 74853 - Lamin A/C globular tail domain | 0 | DIRECT |
46966,51045 46966 - Spectrin repeat 51045 - WW domain | 0 | DIRECT |
101288,50156 101288 - L27 domain 50156 - PDZ domain-like | 0 | DIRECT |
49562,51045 49562 - C2 domain (Calcium/lipid-binding domain, CaLB) 51045 - WW domain | 0 | DIRECT |
50729,50156 50729 - PH domain-like 50156 - PDZ domain-like | 0 | DIRECT |
81324,53850 81324 - Voltage-gated potassium channels 53850 - Periplasmic binding protein-like II | 0 | DIRECT |
49785,49899 49785 - Galactose-binding domain-like 49899 - Concanavalin A-like lectins/glucanases | 0 | DIRECT |
51045,47473 51045 - WW domain 47473 - EF-hand | 0 | DIRECT |
56496,49899 56496 - Fibrinogen C-terminal domain-like 49899 - Concanavalin A-like lectins/glucanases | 0 | DIRECT |
47473,57850 47473 - EF-hand 57850 - RING/U-box | 0 | DIRECT |
48726,82895 48726 - Immunoglobulin 82895 - TSP-1 type 1 repeat | 0 | DIRECT |
63712,90112 63712 - Nicotinic receptor ligand binding domain-like 90112 - Neurotransmitter-gated ion-channel transmembrane pore | 0.0000000001318 | DIRECT |
49899,57196 49899 - Concanavalin A-like lectins/glucanases 57196 - EGF/Laminin | 0.00001159 | DIRECT |
49899,49899 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases | 0.0001592 | DIRECT |
50156,50156 50156 - PDZ domain-like 50156 - PDZ domain-like | 0.0001913 | DIRECT |
101912,103575 101912 - Sema domain 103575 - Plexin repeat | 0.0001913 | DIRECT |
57716,48508 57716 - Glucocorticoid receptor-like (DNA-binding domain) 48508 - Nuclear receptor ligand-binding domain | 0.000222 | DIRECT |
46966,46966 46966 - Spectrin repeat 46966 - Spectrin repeat | 0.0002799 | DIRECT |
63825,57196 63825 - YWTD domain 57196 - EGF/Laminin | 0.0009832 | DIRECT |
47459,158457 47459 - HLH, helix-loop-helix DNA-binding domain 158457 - Orange domain-like | 0.005136 | INHERITED FROM: increased neuron number || increased sensory neuron number |
57424,57184 57424 - LDL receptor-like module 57184 - Growth factor receptor domain | 0.005136 | INHERITED FROM: abnormal cerebellar cortex morphology || abnormal cerebral hemisphere morphology |
57196,57196 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.006123 | INHERITED FROM: abnormal rostral migratory stream morphology || abnormal olfactory lobe morphology || abnormal Schwann cell morphology || abnormal cochlear outer hair cell number || abnormal Bergmann glial cell morphology || abnormal spinal cord commissure morphology || short photoreceptor inner segment || abnormal spinal cord ventral commissure morphology || abnormal cochlear hair cell number || abnormal cochlear inner hair cell number || increased cochlear inner hair cell number || abnormal Muller cell morphology || intracranial hemorrhage |
57424,57424 57424 - LDL receptor-like module 57424 - LDL receptor-like module | 0.009618 | INHERITED FROM: abnormal cerebellum morphology || amyloid beta deposits |
53822,53850 53822 - Periplasmic binding protein-like I 53850 - Periplasmic binding protein-like II | 0.0114 | INHERITED FROM: abnormal NMDA-mediated synaptic currents || abnormal miniature excitatory postsynaptic currents || abnormal nervous system physiology || reduced long term potentiation || abnormal CNS synaptic transmission || abnormal synaptic transmission || abnormal glutamate-mediated receptor currents |
55781,55781 55781 - GAF domain-like 55781 - GAF domain-like | 0.0114 | INHERITED FROM: retinal photoreceptor degeneration || decreased retinal photoreceptor cell number || neuron degeneration || decreased neuron number || abnormal retinal photoreceptor morphology || decreased sensory neuron number |
55781,109604 55781 - GAF domain-like 109604 - HD-domain/PDEase-like | 0.0114 | INHERITED FROM: retinal photoreceptor degeneration || decreased retinal photoreceptor cell number || neuron degeneration || decreased neuron number || abnormal retinal photoreceptor morphology || decreased sensory neuron number |
47986,52129 47986 - DEATH domain 52129 - Caspase-like | 0.0114 | INHERITED FROM: abnormal neuron physiology |
57196,63825 57196 - EGF/Laminin 63825 - YWTD domain | 0.0114 | INHERITED FROM: abnormal cerebellum morphology |
47473,47473 47473 - EF-hand 47473 - EF-hand | 0.01715 | INHERITED FROM: abnormal somatic motor system morphology |
57440,57440 57440 - Kringle-like 57440 - Kringle-like | 0.0194 | INHERITED FROM: altered response to CNS ischemic injury |
57184,49265 57184 - Growth factor receptor domain 49265 - Fibronectin type III | 0.02511 | INHERITED FROM: abnormal sensory neuron morphology || abnormal innervation || abnormal sensory neuron innervation pattern |
63501,50242 63501 - Frizzled cysteine-rich domain 50242 - TIMP-like | 0.02511 | INHERITED FROM: spina bifida || abnormal neural tube morphology || abnormal neural tube closure || open neural tube || craniorachischisis |
81296,81296 81296 - E set domains 81296 - E set domains | 0.03109 | INHERITED FROM: abnormal cerebellar foliation || abnormal cerebellar granule cell morphology || abnormal amacrine cell morphology || ectopic cerebellar granule cells || abnormal hippocampal mossy fiber morphology |
57184,63825 57184 - Growth factor receptor domain 63825 - YWTD domain | 0.03817 | INHERITED FROM: abnormal cerebellar cortex morphology || abnormal cerebral hemisphere morphology |
52058,57184 52058 - L domain-like 57184 - Growth factor receptor domain | 0.03817 | INHERITED FROM: abnormal cerebellar layer morphology || abnormal cerebellar cortex morphology || abnormal somatic sensory system morphology || abnormal somatic nervous system morphology || decreased neuron number || abnormal trigeminal nerve morphology || abnormal nervous system development || abnormal spinal cord morphology || abnormal myelination |
57184,52058 57184 - Growth factor receptor domain 52058 - L domain-like | 0.03817 | INHERITED FROM: abnormal cerebellar layer morphology || abnormal cerebellar cortex morphology || abnormal somatic sensory system morphology || abnormal somatic nervous system morphology || decreased neuron number || abnormal trigeminal nerve morphology || abnormal nervous system development || abnormal spinal cord morphology || abnormal myelination |
89837,89837 89837 - Doublecortin (DC) 89837 - Doublecortin (DC) | 0.03817 | INHERITED FROM: abnormal hippocampus layer morphology || abnormal temporal lobe morphology || abnormal dentate gyrus morphology || abnormal hippocampus morphology |
57196,49899 57196 - EGF/Laminin 49899 - Concanavalin A-like lectins/glucanases | 0.03817 | INHERITED FROM: abnormal embryonic/fetal subventricular zone morphology || abnormal axon guidance |
57196,57184 57196 - EGF/Laminin 57184 - Growth factor receptor domain | 0.04893 | INHERITED FROM: abnormal cochlear inner hair cell morphology || increased neuron number || increased sensory neuron number || abnormal cochlear outer hair cell number || abnormal cochlear outer hair cell morphology || abnormal cochlear hair cell morphology || abnormal cochlear hair cell number || abnormal cochlear inner hair cell number || increased cochlear inner hair cell number |
103575,48726 103575 - Plexin repeat 48726 - Immunoglobulin | 0.04914 | INHERITED FROM: abnormal olfactory lobe morphology || abnormal neuronal migration |
48452,81901 48452 - TPR-like 81901 - HCP-like | 0.05384 | INHERITED FROM: abnormal telencephalon morphology || abnormal neural tube morphology |
57535,49854 57535 - Complement control module/SCR domain 49854 - Spermadhesin, CUB domain | 0.05384 | INHERITED FROM: short excitatory postsynaptic current rise time || biphasic excitatory postsynaptic current amplitude || abnormal Purkinje cell innervation || abnormal excitatory postsynaptic current amplitude || decreased excitatory postsynaptic current amplitude || abnormal excitatory postsynaptic currents || abnormal CNS synaptic transmission || abnormal innervation || abnormal synaptic transmission |
48726,48726 48726 - Immunoglobulin 48726 - Immunoglobulin | 0.0577 | INHERITED FROM: abnormal innervation |
47413,46689 47413 - lambda repressor-like DNA-binding domains 46689 - Homeodomain-like | 0.07198 | INHERITED FROM: abnormal cerebellar foliation || abnormal retinal ganglion cell morphology || cochlear outer hair cell degeneration |
50044,50044 50044 - SH3-domain 50044 - SH3-domain | 0.07198 | INHERITED FROM: abnormal brain commissure morphology |
81324,81324 81324 - Voltage-gated potassium channels 81324 - Voltage-gated potassium channels | 0.08107 | INHERITED FROM: abnormal action potential |
56112,47769 56112 - Protein kinase-like (PK-like) 47769 - SAM/Pointed domain | 0.08156 | INHERITED FROM: abnormal optic tract morphology || decreased corpus callosum size || abnormal axon morphology || abnormal nervous system tract morphology || abnormal axon pruning || abnormal innervation || abnormal brain white matter morphology || abnormal axon guidance |
49417,81296 49417 - p53-like transcription factors 81296 - E set domains | 0.08374 | INHERITED FROM: abnormal spinal cord dorsal column morphology || abnormal spinal cord white matter morphology || abnormal trigeminal nerve morphology || abnormal sensory neuron innervation pattern |
56112,55073 56112 - Protein kinase-like (PK-like) 55073 - Nucleotide cyclase | 0.1405 | INHERITED FROM: abnormal somatic sensory system morphology || abnormal sensory neuron morphology |
49562,48350 49562 - C2 domain (Calcium/lipid-binding domain, CaLB) 48350 - GTPase activation domain, GAP | 0.1405 | INHERITED FROM: abnormal cerebellar layer morphology || abnormal cerebellar cortex morphology || abnormal hindbrain morphology |
52058,48726 52058 - L domain-like 48726 - Immunoglobulin | 0.1928 | INHERITED FROM: abnormal dorsal root ganglion morphology || abnormal telencephalon development |
49313,49313 49313 - Cadherin-like 49313 - Cadherin-like | 0.2126 | INHERITED FROM: abnormal orientation of outer hair cell stereociliary bundles || abnormal cochlear outer hair cell morphology || abnormal cochlear hair cell morphology || abnormal outer hair cell stereociliary bundle morphology || abnormal orientation of cochlear hair cell stereociliary bundles || abnormal cochlear hair cell stereociliary bundle morphology |
57184,57196 57184 - Growth factor receptor domain 57196 - EGF/Laminin | 0.2156 | INHERITED FROM: increased sensory neuron number || increased cochlear hair cell number || abnormal cochlear outer hair cell number || abnormal cochlear hair cell number || abnormal cochlear inner hair cell number || increased cochlear inner hair cell number |
52283,51735 52283 - Formate/glycerate dehydrogenase catalytic domain-like 51735 - NAD(P)-binding Rossmann-fold domains | 0.2347 | INHERITED FROM: abnormal embryonic neuroepithelium morphology |
50044,55550 50044 - SH3-domain 55550 - SH2 domain | 0.3352 | INHERITED FROM: increased dopamine level |
49854,57535 49854 - Spermadhesin, CUB domain 57535 - Complement control module/SCR domain | 0.3399 | INHERITED FROM: short excitatory postsynaptic current rise time || biphasic excitatory postsynaptic current amplitude || abnormal Purkinje cell innervation || abnormal excitatory postsynaptic current amplitude || decreased excitatory postsynaptic current amplitude || abnormal excitatory postsynaptic currents || abnormal innervation |
57586,57586 57586 - TNF receptor-like 57586 - TNF receptor-like | 0.3608 | INHERITED FROM: decreased neuron apoptosis |
81324,81296 81324 - Voltage-gated potassium channels 81296 - E set domains | 0.3608 | INHERITED FROM: tonic-clonic seizures |
57716,57716 57716 - Glucocorticoid receptor-like (DNA-binding domain) 57716 - Glucocorticoid receptor-like (DNA-binding domain) | 0.3705 | INHERITED FROM: abnormal pituitary diverticulum morphology || abnormal Rathke's pouch development || abnormal pituitary gland development |
69318,69179 69318 - Integrin alpha N-terminal domain 69179 - Integrin domains | 0.4323 | INHERITED FROM: axon degeneration |
69179,69179 69179 - Integrin domains 69179 - Integrin domains | 0.4323 | INHERITED FROM: axon degeneration |
49562,49562 49562 - C2 domain (Calcium/lipid-binding domain, CaLB) 49562 - C2 domain (Calcium/lipid-binding domain, CaLB) | 0.5365 | INHERITED FROM: abnormal miniature excitatory postsynaptic currents |
52440,56059 52440 - PreATP-grasp domain 56059 - Glutathione synthetase ATP-binding domain-like | 0.5406 | INHERITED FROM: abnormal synaptic depression || convulsive seizures || abnormal seizure response to inducing agent || tonic-clonic seizures || environmentally induced seizures || abnormal brain wave pattern || increased synaptic depression |
57535,57535 57535 - Complement control module/SCR domain 57535 - Complement control module/SCR domain | 0.8069 | INHERITED FROM: short excitatory postsynaptic current rise time || biphasic excitatory postsynaptic current amplitude || abnormal Purkinje cell innervation || decreased excitatory postsynaptic current amplitude || abnormal excitatory postsynaptic currents |
90123,52540 90123 - ABC transporter transmembrane region 52540 - P-loop containing nucleoside triphosphate hydrolases | 0.808 | INHERITED FROM: amyloid beta deposits || nervous system inclusion bodies |
55550,56112 55550 - SH2 domain 56112 - Protein kinase-like (PK-like) | 0.8414 | INHERITED FROM: delayed neural tube closure |
57667,57667 57667 - beta-beta-alpha zinc fingers 57667 - beta-beta-alpha zinc fingers | 0.8736 | INHERITED FROM: abnormal olfactory nerve morphology |
Supra-domain (Duplex) in N- to C-terminal order |
FDR (all) |
Annotation (direct or inherited) |
55166,51294 55166 - Hedgehog/DD-peptidase 51294 - Hedgehog/intein (Hint) domain | 0 | Direct |
57196,90193 57196 - EGF/Laminin 90193 - Notch domain | 0 | Direct |
57184,49899 57184 - Growth factor receptor domain 49899 - Concanavalin A-like lectins/glucanases | 0 | Direct |
90193,90193 90193 - Notch domain 90193 - Notch domain | 0 | Direct |
46785,144074 46785 - "Winged helix" DNA-binding domain 144074 - E2F-DP heterodimerization region | 0 | Direct |
50044,50156 50044 - SH3-domain 50156 - PDZ domain-like | 0 | Direct |
51556,51338 51556 - Metallo-dependent hydrolases 51338 - Composite domain of metallo-dependent hydrolases | 0 | Direct |
57196,56496 57196 - EGF/Laminin 56496 - Fibrinogen C-terminal domain-like | 0 | Direct |
57196,57424 57196 - EGF/Laminin 57424 - LDL receptor-like module | 0 | Direct |
51338,51556 51338 - Composite domain of metallo-dependent hydrolases 51556 - Metallo-dependent hydrolases | 0 | Direct |
81296,101898 81296 - E set domains 101898 - NHL repeat | 0 | Direct |
50729,57889 50729 - PH domain-like 57889 - Cysteine-rich domain | 0 | Direct |
64593,74853 64593 - Intermediate filament protein, coiled coil region 74853 - Lamin A/C globular tail domain | 0 | Direct |
46966,51045 46966 - Spectrin repeat 51045 - WW domain | 0 | Direct |
101288,50156 101288 - L27 domain 50156 - PDZ domain-like | 0 | Direct |
49562,51045 49562 - C2 domain (Calcium/lipid-binding domain, CaLB) 51045 - WW domain | 0 | Direct |
50729,50156 50729 - PH domain-like 50156 - PDZ domain-like | 0 | Direct |
81324,53850 81324 - Voltage-gated potassium channels 53850 - Periplasmic binding protein-like II | 0 | Direct |
49785,49899 49785 - Galactose-binding domain-like 49899 - Concanavalin A-like lectins/glucanases | 0 | Direct |
51045,47473 51045 - WW domain 47473 - EF-hand | 0 | Direct |
56496,49899 56496 - Fibrinogen C-terminal domain-like 49899 - Concanavalin A-like lectins/glucanases | 0 | Direct |
47473,57850 47473 - EF-hand 57850 - RING/U-box | 0 | Direct |
48726,82895 48726 - Immunoglobulin 82895 - TSP-1 type 1 repeat | 0 | Direct |
63712,90112 63712 - Nicotinic receptor ligand binding domain-like 90112 - Neurotransmitter-gated ion-channel transmembrane pore | 0.0000000001318 | Direct |
49899,57196 49899 - Concanavalin A-like lectins/glucanases 57196 - EGF/Laminin | 0.00001159 | Direct |
49899,49899 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases | 0.0001592 | Direct |
50156,50156 50156 - PDZ domain-like 50156 - PDZ domain-like | 0.0001913 | Direct |
101912,103575 101912 - Sema domain 103575 - Plexin repeat | 0.0001913 | Direct |
57716,48508 57716 - Glucocorticoid receptor-like (DNA-binding domain) 48508 - Nuclear receptor ligand-binding domain | 0.000222 | Direct |
46966,46966 46966 - Spectrin repeat 46966 - Spectrin repeat | 0.0002799 | Direct |
63825,57196 63825 - YWTD domain 57196 - EGF/Laminin | 0.0009832 | Direct |
47459,158457 47459 - HLH, helix-loop-helix DNA-binding domain 158457 - Orange domain-like | 0.005136 | Inherited |
57424,57184 57424 - LDL receptor-like module 57184 - Growth factor receptor domain | 0.005136 | Inherited |
57196,57196 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.006123 | Inherited |
57424,57424 57424 - LDL receptor-like module 57424 - LDL receptor-like module | 0.009618 | Inherited |
53822,53850 53822 - Periplasmic binding protein-like I 53850 - Periplasmic binding protein-like II | 0.0114 | Inherited |
55781,55781 55781 - GAF domain-like 55781 - GAF domain-like | 0.0114 | Inherited |
55781,109604 55781 - GAF domain-like 109604 - HD-domain/PDEase-like | 0.0114 | Inherited |
47986,52129 47986 - DEATH domain 52129 - Caspase-like | 0.0114 | Inherited |
57196,63825 57196 - EGF/Laminin 63825 - YWTD domain | 0.0114 | Inherited |
47473,47473 47473 - EF-hand 47473 - EF-hand | 0.01715 | Inherited |
57440,57440 57440 - Kringle-like 57440 - Kringle-like | 0.0194 | Inherited |
57184,49265 57184 - Growth factor receptor domain 49265 - Fibronectin type III | 0.02511 | Inherited |
63501,50242 63501 - Frizzled cysteine-rich domain 50242 - TIMP-like | 0.02511 | Inherited |
81296,81296 81296 - E set domains 81296 - E set domains | 0.03109 | Inherited |
57184,63825 57184 - Growth factor receptor domain 63825 - YWTD domain | 0.03817 | Inherited |
52058,57184 52058 - L domain-like 57184 - Growth factor receptor domain | 0.03817 | Inherited |
57184,52058 57184 - Growth factor receptor domain 52058 - L domain-like | 0.03817 | Inherited |
89837,89837 89837 - Doublecortin (DC) 89837 - Doublecortin (DC) | 0.03817 | Inherited |
57196,49899 57196 - EGF/Laminin 49899 - Concanavalin A-like lectins/glucanases | 0.03817 | Inherited |
57196,57184 57196 - EGF/Laminin 57184 - Growth factor receptor domain | 0.04893 | Inherited |
103575,48726 103575 - Plexin repeat 48726 - Immunoglobulin | 0.04914 | Inherited |
48452,81901 48452 - TPR-like 81901 - HCP-like | 0.05384 | Inherited |
57535,49854 57535 - Complement control module/SCR domain 49854 - Spermadhesin, CUB domain | 0.05384 | Inherited |
48726,48726 48726 - Immunoglobulin 48726 - Immunoglobulin | 0.0577 | Inherited |
47413,46689 47413 - lambda repressor-like DNA-binding domains 46689 - Homeodomain-like | 0.07198 | Inherited |
50044,50044 50044 - SH3-domain 50044 - SH3-domain | 0.07198 | Inherited |
81324,81324 81324 - Voltage-gated potassium channels 81324 - Voltage-gated potassium channels | 0.08107 | Inherited |
56112,47769 56112 - Protein kinase-like (PK-like) 47769 - SAM/Pointed domain | 0.08156 | Inherited |
49417,81296 49417 - p53-like transcription factors 81296 - E set domains | 0.08374 | Inherited |
56112,55073 56112 - Protein kinase-like (PK-like) 55073 - Nucleotide cyclase | 0.1405 | Inherited |
49562,48350 49562 - C2 domain (Calcium/lipid-binding domain, CaLB) 48350 - GTPase activation domain, GAP | 0.1405 | Inherited |
52058,48726 52058 - L domain-like 48726 - Immunoglobulin | 0.1928 | Inherited |
49313,49313 49313 - Cadherin-like 49313 - Cadherin-like | 0.2126 | Inherited |
57184,57196 57184 - Growth factor receptor domain 57196 - EGF/Laminin | 0.2156 | Inherited |
52283,51735 52283 - Formate/glycerate dehydrogenase catalytic domain-like 51735 - NAD(P)-binding Rossmann-fold domains | 0.2347 | Inherited |
50044,55550 50044 - SH3-domain 55550 - SH2 domain | 0.3352 | Inherited |
49854,57535 49854 - Spermadhesin, CUB domain 57535 - Complement control module/SCR domain | 0.3399 | Inherited |
57586,57586 57586 - TNF receptor-like 57586 - TNF receptor-like | 0.3608 | Inherited |
81324,81296 81324 - Voltage-gated potassium channels 81296 - E set domains | 0.3608 | Inherited |
57716,57716 57716 - Glucocorticoid receptor-like (DNA-binding domain) 57716 - Glucocorticoid receptor-like (DNA-binding domain) | 0.3705 | Inherited |
69318,69179 69318 - Integrin alpha N-terminal domain 69179 - Integrin domains | 0.4323 | Inherited |
69179,69179 69179 - Integrin domains 69179 - Integrin domains | 0.4323 | Inherited |
49562,49562 49562 - C2 domain (Calcium/lipid-binding domain, CaLB) 49562 - C2 domain (Calcium/lipid-binding domain, CaLB) | 0.5365 | Inherited |
52440,56059 52440 - PreATP-grasp domain 56059 - Glutathione synthetase ATP-binding domain-like | 0.5406 | Inherited |
57535,57535 57535 - Complement control module/SCR domain 57535 - Complement control module/SCR domain | 0.8069 | Inherited |
90123,52540 90123 - ABC transporter transmembrane region 52540 - P-loop containing nucleoside triphosphate hydrolases | 0.808 | Inherited |
55550,56112 55550 - SH2 domain 56112 - Protein kinase-like (PK-like) | 0.8414 | Inherited |
57667,57667 57667 - beta-beta-alpha zinc fingers 57667 - beta-beta-alpha zinc fingers | 0.8736 | Inherited |
(show details)
Supra-domains annotated to this MP term (Not in SPMP)
Highlighted in gray are those with FDR>0.001
Supra-domain (Triple) in N- to C-terminal order |
FDR (all) |
Annotation (direct or inherited) |
63411,63411,63411 63411 - LuxS/MPP-like metallohydrolase 63411 - LuxS/MPP-like metallohydrolase 63411 - LuxS/MPP-like metallohydrolase | 0 | DIRECT |
101288,50156,50044 101288 - L27 domain 50156 - PDZ domain-like 50044 - SH3-domain | 0 | DIRECT |
57184,52058,57184 57184 - Growth factor receptor domain 52058 - L domain-like 57184 - Growth factor receptor domain | 0 | DIRECT |
63825,57196,57424 63825 - YWTD domain 57196 - EGF/Laminin 57424 - LDL receptor-like module | 0 | DIRECT |
56496,49899,49899 56496 - Fibrinogen C-terminal domain-like 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases | 0 | DIRECT |
49785,49899,49899 49785 - Galactose-binding domain-like 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases | 0 | DIRECT |
57196,56496,49899 57196 - EGF/Laminin 56496 - Fibrinogen C-terminal domain-like 49899 - Concanavalin A-like lectins/glucanases | 0 | DIRECT |
57196,57424,57424 57196 - EGF/Laminin 57424 - LDL receptor-like module 57424 - LDL receptor-like module | 0 | DIRECT |
46966,51045,47473 46966 - Spectrin repeat 51045 - WW domain 47473 - EF-hand | 0 | DIRECT |
75399,75399,75399 75399 - Plakin repeat 75399 - Plakin repeat 75399 - Plakin repeat | 0 | DIRECT |
51045,47473,47473 51045 - WW domain 47473 - EF-hand 47473 - EF-hand | 0 | DIRECT |
57196,90193,90193 57196 - EGF/Laminin 90193 - Notch domain 90193 - Notch domain | 0 | DIRECT |
52058,48726,48726 52058 - L domain-like 48726 - Immunoglobulin 48726 - Immunoglobulin | 0 | DIRECT |
48726,82895,82895 48726 - Immunoglobulin 82895 - TSP-1 type 1 repeat 82895 - TSP-1 type 1 repeat | 0 | DIRECT |
51338,51556,51338 51338 - Composite domain of metallo-dependent hydrolases 51556 - Metallo-dependent hydrolases 51338 - Composite domain of metallo-dependent hydrolases | 0 | DIRECT |
49503,49503,49503 49503 - Cupredoxins 49503 - Cupredoxins 49503 - Cupredoxins | 0 | DIRECT |
50729,50156,50156 50729 - PH domain-like 50156 - PDZ domain-like 50156 - PDZ domain-like | 0 | DIRECT |
46966,46966,51045 46966 - Spectrin repeat 46966 - Spectrin repeat 51045 - WW domain | 0 | DIRECT |
57184,49899,49899 57184 - Growth factor receptor domain 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases | 0 | DIRECT |
47473,47473,57850 47473 - EF-hand 47473 - EF-hand 57850 - RING/U-box | 0 | DIRECT |
49899,57196,56496 49899 - Concanavalin A-like lectins/glucanases 57196 - EGF/Laminin 56496 - Fibrinogen C-terminal domain-like | 0 | DIRECT |
48726,48726,82895 48726 - Immunoglobulin 48726 - Immunoglobulin 82895 - TSP-1 type 1 repeat | 0 | DIRECT |
49899,49899,57196 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases 57196 - EGF/Laminin | 0 | DIRECT |
48726,48726,48726 48726 - Immunoglobulin 48726 - Immunoglobulin 48726 - Immunoglobulin | 0.0004072 | DIRECT |
57196,57196,57196 57196 - EGF/Laminin 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.0004139 | DIRECT |
46966,46966,46966 46966 - Spectrin repeat 46966 - Spectrin repeat 46966 - Spectrin repeat | 0.0004661 | DIRECT |
49899,49899,49899 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases | 0.002193 | INHERITED FROM: reduced NMDA-mediated synaptic currents || abnormal synaptic depression || abnormal NMDA-mediated synaptic currents || abnormal excitatory postsynaptic current amplitude || decreased excitatory postsynaptic current amplitude || abnormal GABA-mediated receptor currents || abnormal paired-pulse inhibition || abnormal AMPA-mediated synaptic currents || decreased CNS synapse formation || reduced AMPA-mediated synaptic currents || abnormal glutamate-mediated receptor currents || abnormal CNS synapse formation || abnormal nervous system morphology || decreased neurotransmitter release |
49899,57196,57196 49899 - Concanavalin A-like lectins/glucanases 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.002263 | INHERITED FROM: abnormal amacrine cell morphology || abnormal retinal bipolar cell morphology || abnormal nervous system morphology |
57196,57196,57184 57196 - EGF/Laminin 57196 - EGF/Laminin 57184 - Growth factor receptor domain | 0.0034 | INHERITED FROM: abnormal cochlear inner hair cell morphology || increased sensory neuron number || abnormal cochlear outer hair cell number || abnormal cochlear outer hair cell morphology || abnormal somatic sensory system morphology || abnormal cochlear hair cell morphology || increased cochlear outer hair cell number || abnormal cochlear hair cell number || abnormal cochlear inner hair cell number || increased cochlear inner hair cell number || abnormal nervous system morphology |
81296,81296,81296 81296 - E set domains 81296 - E set domains 81296 - E set domains | 0.0034 | INHERITED FROM: abnormal telencephalon morphology || abnormal cerebellar foliation || abnormal cerebellar granule cell morphology || abnormal cerebellar granule layer morphology || abnormal amacrine cell morphology || ectopic cerebellar granule cells || abnormal brain commissure morphology || abnormal cerebral hemisphere morphology || abnormal hippocampal mossy fiber morphology || abnormal nervous system morphology |
48726,48726,49265 48726 - Immunoglobulin 48726 - Immunoglobulin 49265 - Fibronectin type III | 0.003926 | INHERITED FROM: abnormal telencephalon morphology || abnormal metencephalon morphology || abnormal neuron differentiation || abnormal brain commissure morphology |
57424,57424,57424 57424 - LDL receptor-like module 57424 - LDL receptor-like module 57424 - LDL receptor-like module | 0.00442 | INHERITED FROM: abnormal metencephalon morphology || abnormal cerebellum morphology || amyloid beta deposits || abnormal nervous system morphology |
50044,50044,50044 50044 - SH3-domain 50044 - SH3-domain 50044 - SH3-domain | 0.0114 | INHERITED FROM: abnormal nervous system tract morphology || abnormal brain white matter morphology || abnormal brain commissure morphology |
55781,55781,109604 55781 - GAF domain-like 55781 - GAF domain-like 109604 - HD-domain/PDEase-like | 0.0114 | INHERITED FROM: retinal photoreceptor degeneration || decreased retinal photoreceptor cell number || neuron degeneration || decreased neuron number || abnormal retinal photoreceptor morphology || decreased sensory neuron number |
57424,57184,63825 57424 - LDL receptor-like module 57184 - Growth factor receptor domain 63825 - YWTD domain | 0.0114 | INHERITED FROM: abnormal telencephalon morphology || abnormal cerebellum morphology || abnormal cerebellar cortex morphology || abnormal cerebral hemisphere morphology |
57424,57424,57184 57424 - LDL receptor-like module 57424 - LDL receptor-like module 57184 - Growth factor receptor domain | 0.0114 | INHERITED FROM: abnormal telencephalon morphology || abnormal cerebellum morphology || abnormal cerebellar cortex morphology || abnormal cerebral hemisphere morphology |
48065,50729,50044 48065 - DBL homology domain (DH-domain) 50729 - PH domain-like 50044 - SH3-domain | 0.02511 | INHERITED FROM: abnormal nervous system development |
52058,57184,52058 52058 - L domain-like 57184 - Growth factor receptor domain 52058 - L domain-like | 0.03817 | INHERITED FROM: abnormal cerebellar layer morphology || abnormal cerebellar cortex morphology || abnormal somatic sensory system morphology || abnormal somatic nervous system morphology || decreased neuron number || abnormal trigeminal nerve morphology || abnormal nervous system development || abnormal spinal cord morphology || abnormal myelination |
101912,103575,48726 101912 - Sema domain 103575 - Plexin repeat 48726 - Immunoglobulin | 0.04914 | INHERITED FROM: abnormal olfactory lobe morphology || abnormal neuronal migration |
57184,57196,57196 57184 - Growth factor receptor domain 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.0507 | INHERITED FROM: abnormal cochlear inner hair cell morphology || increased cochlear hair cell number || abnormal cochlear outer hair cell number || abnormal cochlear outer hair cell morphology || abnormal cochlear hair cell morphology || abnormal cochlear hair cell number || abnormal cochlear inner hair cell number || increased cochlear inner hair cell number |
57535,49854,57535 57535 - Complement control module/SCR domain 49854 - Spermadhesin, CUB domain 57535 - Complement control module/SCR domain | 0.05384 | INHERITED FROM: short excitatory postsynaptic current rise time || biphasic excitatory postsynaptic current amplitude || abnormal Purkinje cell innervation || abnormal excitatory postsynaptic current amplitude || decreased excitatory postsynaptic current amplitude || abnormal excitatory postsynaptic currents || abnormal CNS synaptic transmission || abnormal innervation || abnormal synaptic transmission |
49854,57535,49854 49854 - Spermadhesin, CUB domain 57535 - Complement control module/SCR domain 49854 - Spermadhesin, CUB domain | 0.05384 | INHERITED FROM: short excitatory postsynaptic current rise time || biphasic excitatory postsynaptic current amplitude || abnormal Purkinje cell innervation || abnormal excitatory postsynaptic current amplitude || decreased excitatory postsynaptic current amplitude || abnormal excitatory postsynaptic currents || abnormal CNS synaptic transmission || abnormal innervation || abnormal synaptic transmission |
57196,57184,57196 57196 - EGF/Laminin 57184 - Growth factor receptor domain 57196 - EGF/Laminin | 0.1337 | INHERITED FROM: abnormal cochlear inner hair cell morphology || increased neuron number || increased sensory neuron number || increased cochlear hair cell number || abnormal mechanoreceptor morphology || abnormal cochlear outer hair cell number || abnormal cochlear outer hair cell morphology || abnormal cochlear hair cell morphology || abnormal cochlear hair cell number || abnormal cochlear inner hair cell number || increased cochlear inner hair cell number |
49854,57535,57535 49854 - Spermadhesin, CUB domain 57535 - Complement control module/SCR domain 57535 - Complement control module/SCR domain | 0.2347 | INHERITED FROM: short excitatory postsynaptic current rise time || biphasic excitatory postsynaptic current amplitude || abnormal Purkinje cell innervation || abnormal excitatory postsynaptic current amplitude || decreased excitatory postsynaptic current amplitude || abnormal excitatory postsynaptic currents || abnormal innervation |
69179,69179,69179 69179 - Integrin domains 69179 - Integrin domains 69179 - Integrin domains | 0.3003 | INHERITED FROM: axon degeneration |
49313,49313,49313 49313 - Cadherin-like 49313 - Cadherin-like 49313 - Cadherin-like | 0.3324 | INHERITED FROM: abnormal orientation of outer hair cell stereociliary bundles || abnormal cochlear outer hair cell morphology || abnormal cochlear hair cell morphology || abnormal outer hair cell stereociliary bundle morphology || abnormal orientation of cochlear hair cell stereociliary bundles || abnormal cochlear hair cell stereociliary bundle morphology |
69318,69179,69179 69318 - Integrin alpha N-terminal domain 69179 - Integrin domains 69179 - Integrin domains | 0.4323 | INHERITED FROM: axon degeneration |
57535,57535,57535 57535 - Complement control module/SCR domain 57535 - Complement control module/SCR domain 57535 - Complement control module/SCR domain | 0.6058 | INHERITED FROM: short excitatory postsynaptic current rise time || biphasic excitatory postsynaptic current amplitude || abnormal Purkinje cell innervation || abnormal excitatory postsynaptic current amplitude || decreased excitatory postsynaptic current amplitude |
50044,55550,56112 50044 - SH3-domain 55550 - SH2 domain 56112 - Protein kinase-like (PK-like) | 0.665 | INHERITED FROM: delayed neural tube closure || ectopic neuron |
57667,57667,57667 57667 - beta-beta-alpha zinc fingers 57667 - beta-beta-alpha zinc fingers 57667 - beta-beta-alpha zinc fingers | 0.972 | INHERITED FROM: abnormal neuron proliferation || absent floor plate |
Supra-domain (Triple) in N- to C-terminal order |
FDR (all) |
Annotation (direct or inherited) |
63411,63411,63411 63411 - LuxS/MPP-like metallohydrolase 63411 - LuxS/MPP-like metallohydrolase 63411 - LuxS/MPP-like metallohydrolase | 0 | Direct |
101288,50156,50044 101288 - L27 domain 50156 - PDZ domain-like 50044 - SH3-domain | 0 | Direct |
57184,52058,57184 57184 - Growth factor receptor domain 52058 - L domain-like 57184 - Growth factor receptor domain | 0 | Direct |
63825,57196,57424 63825 - YWTD domain 57196 - EGF/Laminin 57424 - LDL receptor-like module | 0 | Direct |
56496,49899,49899 56496 - Fibrinogen C-terminal domain-like 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases | 0 | Direct |
49785,49899,49899 49785 - Galactose-binding domain-like 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases | 0 | Direct |
57196,56496,49899 57196 - EGF/Laminin 56496 - Fibrinogen C-terminal domain-like 49899 - Concanavalin A-like lectins/glucanases | 0 | Direct |
57196,57424,57424 57196 - EGF/Laminin 57424 - LDL receptor-like module 57424 - LDL receptor-like module | 0 | Direct |
46966,51045,47473 46966 - Spectrin repeat 51045 - WW domain 47473 - EF-hand | 0 | Direct |
75399,75399,75399 75399 - Plakin repeat 75399 - Plakin repeat 75399 - Plakin repeat | 0 | Direct |
51045,47473,47473 51045 - WW domain 47473 - EF-hand 47473 - EF-hand | 0 | Direct |
57196,90193,90193 57196 - EGF/Laminin 90193 - Notch domain 90193 - Notch domain | 0 | Direct |
52058,48726,48726 52058 - L domain-like 48726 - Immunoglobulin 48726 - Immunoglobulin | 0 | Direct |
48726,82895,82895 48726 - Immunoglobulin 82895 - TSP-1 type 1 repeat 82895 - TSP-1 type 1 repeat | 0 | Direct |
51338,51556,51338 51338 - Composite domain of metallo-dependent hydrolases 51556 - Metallo-dependent hydrolases 51338 - Composite domain of metallo-dependent hydrolases | 0 | Direct |
49503,49503,49503 49503 - Cupredoxins 49503 - Cupredoxins 49503 - Cupredoxins | 0 | Direct |
50729,50156,50156 50729 - PH domain-like 50156 - PDZ domain-like 50156 - PDZ domain-like | 0 | Direct |
46966,46966,51045 46966 - Spectrin repeat 46966 - Spectrin repeat 51045 - WW domain | 0 | Direct |
57184,49899,49899 57184 - Growth factor receptor domain 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases | 0 | Direct |
47473,47473,57850 47473 - EF-hand 47473 - EF-hand 57850 - RING/U-box | 0 | Direct |
49899,57196,56496 49899 - Concanavalin A-like lectins/glucanases 57196 - EGF/Laminin 56496 - Fibrinogen C-terminal domain-like | 0 | Direct |
48726,48726,82895 48726 - Immunoglobulin 48726 - Immunoglobulin 82895 - TSP-1 type 1 repeat | 0 | Direct |
49899,49899,57196 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases 57196 - EGF/Laminin | 0 | Direct |
48726,48726,48726 48726 - Immunoglobulin 48726 - Immunoglobulin 48726 - Immunoglobulin | 0.0004072 | Direct |
57196,57196,57196 57196 - EGF/Laminin 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.0004139 | Direct |
46966,46966,46966 46966 - Spectrin repeat 46966 - Spectrin repeat 46966 - Spectrin repeat | 0.0004661 | Direct |
49899,49899,49899 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases | 0.002193 | Inherited |
49899,57196,57196 49899 - Concanavalin A-like lectins/glucanases 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.002263 | Inherited |
57196,57196,57184 57196 - EGF/Laminin 57196 - EGF/Laminin 57184 - Growth factor receptor domain | 0.0034 | Inherited |
81296,81296,81296 81296 - E set domains 81296 - E set domains 81296 - E set domains | 0.0034 | Inherited |
48726,48726,49265 48726 - Immunoglobulin 48726 - Immunoglobulin 49265 - Fibronectin type III | 0.003926 | Inherited |
57424,57424,57424 57424 - LDL receptor-like module 57424 - LDL receptor-like module 57424 - LDL receptor-like module | 0.00442 | Inherited |
50044,50044,50044 50044 - SH3-domain 50044 - SH3-domain 50044 - SH3-domain | 0.0114 | Inherited |
55781,55781,109604 55781 - GAF domain-like 55781 - GAF domain-like 109604 - HD-domain/PDEase-like | 0.0114 | Inherited |
57424,57184,63825 57424 - LDL receptor-like module 57184 - Growth factor receptor domain 63825 - YWTD domain | 0.0114 | Inherited |
57424,57424,57184 57424 - LDL receptor-like module 57424 - LDL receptor-like module 57184 - Growth factor receptor domain | 0.0114 | Inherited |
48065,50729,50044 48065 - DBL homology domain (DH-domain) 50729 - PH domain-like 50044 - SH3-domain | 0.02511 | Inherited |
52058,57184,52058 52058 - L domain-like 57184 - Growth factor receptor domain 52058 - L domain-like | 0.03817 | Inherited |
101912,103575,48726 101912 - Sema domain 103575 - Plexin repeat 48726 - Immunoglobulin | 0.04914 | Inherited |
57184,57196,57196 57184 - Growth factor receptor domain 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.0507 | Inherited |
57535,49854,57535 57535 - Complement control module/SCR domain 49854 - Spermadhesin, CUB domain 57535 - Complement control module/SCR domain | 0.05384 | Inherited |
49854,57535,49854 49854 - Spermadhesin, CUB domain 57535 - Complement control module/SCR domain 49854 - Spermadhesin, CUB domain | 0.05384 | Inherited |
57196,57184,57196 57196 - EGF/Laminin 57184 - Growth factor receptor domain 57196 - EGF/Laminin | 0.1337 | Inherited |
49854,57535,57535 49854 - Spermadhesin, CUB domain 57535 - Complement control module/SCR domain 57535 - Complement control module/SCR domain | 0.2347 | Inherited |
69179,69179,69179 69179 - Integrin domains 69179 - Integrin domains 69179 - Integrin domains | 0.3003 | Inherited |
49313,49313,49313 49313 - Cadherin-like 49313 - Cadherin-like 49313 - Cadherin-like | 0.3324 | Inherited |
69318,69179,69179 69318 - Integrin alpha N-terminal domain 69179 - Integrin domains 69179 - Integrin domains | 0.4323 | Inherited |
57535,57535,57535 57535 - Complement control module/SCR domain 57535 - Complement control module/SCR domain 57535 - Complement control module/SCR domain | 0.6058 | Inherited |
50044,55550,56112 50044 - SH3-domain 55550 - SH2 domain 56112 - Protein kinase-like (PK-like) | 0.665 | Inherited |
57667,57667,57667 57667 - beta-beta-alpha zinc fingers 57667 - beta-beta-alpha zinc fingers 57667 - beta-beta-alpha zinc fingers | 0.972 | Inherited |
Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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Trees by TreeVector
A presence/absence matrix is generated using protein domains and supradomains
for all genomes in SUPERFAMILY. The RAxML
software is used to produce a single, large tree topology using
heuristic parsimony methods. Genome combinations, or specific clades, can be displayed as
if individual trees had been produced. However, this data is extracted from the single
large tree. This produces a higher quality topology than if the trees had been produced
on their own, and allows the trees to be displayed instantly.
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