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Mammalian Phenotype (MP): abnormal nervous system morphology
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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 (Not in SDMP)
Highlighted in gray are those with FDR_all>0.001
Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]
Family(show details)
Family domains annotated to this MP term (Not in SDMP)
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 |
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 |
Homeodomain | 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 |
Sema domain | 0.00001413 | DIRECT |
Frizzled cysteine-rich domain | 0.00003812 | DIRECT |
Spectrin repeat | 0.00005865 | DIRECT |
Laminin-type module | 0.00009245 | DIRECT |
Ephrin ectodomain | 0.002174 | INHERITED FROM: abnormal neuron morphology || abnormal thalamus morphology || abnormal axon morphology || abnormal olfactory bulb morphology |
Paired domain | 0.003835 | INHERITED FROM: abnormal somatic sensory system morphology || abnormal midbrain morphology || abnormal brain ventricle morphology || abnormal brainstem morphology |
Cell cycle transcription factor e2f-dp | 0.003835 | INHERITED FROM: abnormal retinal bipolar cell morphology || decreased retinal ganglion cell number || decreased sensory neuron number || abnormal retinal ganglion cell morphology |
DIX domain | 0.005619 | INHERITED FROM: abnormal orientation of cochlear hair cell stereociliary bundles || abnormal mechanoreceptor morphology || increased neuron number || abnormal brain morphology || abnormal cochlear hair cell stereociliary bundle morphology || abnormal hair cell morphology || craniorachischisis || abnormal cochlear hair cell morphology || abnormal neural tube closure || abnormal cochlear outer hair cell morphology || increased cochlear hair cell number || abnormal neural tube morphology || abnormal nervous system development || increased sensory neuron number || abnormal cochlear hair cell number || exencephaly |
SMAD MH1 domain | 0.008917 | INHERITED FROM: abnormal brain morphology || abnormal nervous system development |
SMAD domain | 0.008917 | INHERITED FROM: abnormal brain morphology || abnormal nervous system development |
L domain | 0.02 | INHERITED FROM: abnormal somatic nervous system morphology || abnormal somatic sensory system morphology || abnormal spinal cord morphology || abnormal trigeminal nerve morphology || abnormal cerebellar layer morphology || abnormal nervous system development || decreased neuron number |
Doublecortin (DC) | 0.02 | INHERITED FROM: abnormal dentate gyrus morphology || abnormal hippocampus layer morphology |
Forkhead DNA-binding domain | 0.02115 | INHERITED FROM: abnormal radial glial cell morphology || holoprosencephaly |
Laminin G-like module | 0.02808 | INHERITED FROM: abnormal spinal cord ventral commissure morphology || abnormal Schwann cell morphology || abnormal CNS synapse formation || abnormal spinal cord commissure morphology || decreased CNS synapse formation || abnormal spinal cord lateral column morphology |
Plexin repeat | 0.03239 | INHERITED FROM: abnormal neuron morphology || abnormal cerebellar granule cell morphology || ectopic cerebellar granule cells || abnormal telencephalon morphology || ectopic neuron || abnormal cerebellar granule layer morphology || abnormal hippocampal mossy fiber morphology || abnormal amacrine cell morphology || abnormal cerebellar cortex morphology |
Formate/glycerate dehydrogenases, substrate-binding domain | 0.0343 | INHERITED FROM: abnormal embryonic neuroepithelium morphology || abnormal neural tube morphology |
beta-glycanases | 0.0343 | INHERITED FROM: abnormal striatum morphology || abnormal cerebellum morphology || abnormal telencephalon morphology || abnormal cerebral hemisphere morphology || abnormal temporal lobe morphology || abnormal hippocampus morphology || abnormal hindbrain morphology || abnormal basal ganglion morphology || abnormal metencephalon morphology || abnormal limbic system morphology |
GDNF receptor-like | 0.0343 | INHERITED FROM: abnormal somatic sensory system morphology || abnormal autonomic nervous system morphology |
Mib/herc2 domain | 0.0343 | INHERITED FROM: abnormal brain development |
Multidrug efflux transporter AcrB transmembrane domain | 0.0343 | INHERITED FROM: abnormal diencephalon morphology |
SRF-like | 0.0343 | INHERITED FROM: decreased brain size || abnormal brain size |
HMA, heavy metal-associated domain | 0.0343 | INHERITED FROM: abnormal brain copper level |
Ephrin receptor ligand binding domain | 0.03672 | INHERITED FROM: abnormal axon guidance || decreased corpus callosum size || abnormal axon morphology || abnormal brain white matter morphology || abnormal nervous system tract morphology || abnormal innervation || abnormal axon pruning || abnormal optic tract morphology |
Clc chloride channel | 0.04497 | INHERITED FROM: abnormal photoreceptor outer segment morphology || abnormal retinal photoreceptor morphology || abnormal photoreceptor inner segment morphology |
POU-specific domain | 0.05074 | INHERITED FROM: abnormal cerebellar foliation || cochlear outer hair cell degeneration || abnormal retinal ganglion cell morphology || abnormal cerebellum lobule morphology |
Fibronectin type III | 0.05765 | INHERITED FROM: abnormal axon guidance |
Bcl-2 inhibitors of programmed cell death | 0.08084 | INHERITED FROM: abnormal autonomic nervous system morphology || abnormal pons morphology || abnormal metencephalon morphology |
Cap-Gly domain | 0.08794 | INHERITED FROM: abnormal spinal cord grey matter morphology || abnormal motor neuron morphology |
Cadherin | 0.1009 | INHERITED FROM: abnormal orientation of cochlear hair cell stereociliary bundles || abnormal outer hair cell stereociliary bundle morphology || abnormal cochlear hair cell stereociliary bundle morphology || abnormal cochlear hair cell morphology || abnormal orientation of outer hair cell stereociliary bundles || abnormal cochlear outer hair cell morphology |
HLH, helix-loop-helix DNA-binding domain | 0.1062 | INHERITED FROM: abnormal amacrine cell number || absent choroid plexus || abnormal retinal bipolar cell morphology || increased neuron number || decreased amacrine cell number || pituitary gland hypoplasia || premature neuronal precursor differentiation || abnormal Muller cell morphology || abnormal neuron differentiation || abnormal horizontal cell morphology || abnormal amacrine cell morphology || absent oligodendrocytes || decreased oligodendrocyte number || abnormal nervous system development || increased sensory neuron number || abnormal Cajal-Retzius cell morphology || abnormal neuroendocrine cell morphology || abnormal neurohypophysis morphology |
CBS-domain pair | 0.1102 | INHERITED FROM: abnormal photoreceptor outer segment morphology || abnormal retinal photoreceptor morphology || abnormal astrocyte morphology || abnormal astrocyte number || increased astrocyte number || abnormal photoreceptor inner segment morphology |
Growth factor receptor domain | 0.122 | INHERITED FROM: abnormal cochlear hair cell morphology || abnormal cochlear inner hair cell number || abnormal cochlear outer hair cell morphology || abnormal nervous system development |
SH3-domain | 0.1311 | INHERITED FROM: abnormal hippocampus pyramidal cell layer || short cochlear hair cell stereocilia |
Transforming growth factor (TGF)-beta | 0.158 | INHERITED FROM: abnormal enteric nervous system morphology || abnormal enteric neuron morphology |
Formate/glycerate dehydrogenases, NAD-domain | 0.1643 | INHERITED FROM: abnormal embryonic neuroepithelium morphology |
Acetylcholinesterase-like | 0.1792 | INHERITED FROM: abnormal synaptic bouton morphology || abnormal synapse morphology |
Cyclin | 0.1915 | INHERITED FROM: ectopic Purkinje cell || small cerebellum || abnormal cerebellar foliation || abnormal cerebellum lobule morphology || absent Purkinje cell layer |
FYVE, a phosphatidylinositol-3-phosphate binding domain | 0.2041 | INHERITED FROM: abnormal spinal cord morphology |
I set domains | 0.212 | INHERITED FROM: abnormal paranode morphology || abnormal innervation |
EGF-type module | 0.2224 | INHERITED FROM: abnormal olfactory tract morphology || abnormal spinal cord ventral commissure morphology || fused dorsal root ganglion || abnormal spinal cord commissure morphology || abnormal cochlear inner hair cell number || increased sensory neuron number || increased cochlear inner hair cell number || abnormal spinal cord lateral column morphology |
YWTD domain | 0.2612 | INHERITED FROM: abnormal cerebellum morphology || amyloid beta deposits || abnormal metencephalon morphology |
p120GAP domain-like | 0.2802 | INHERITED FROM: abnormal dendrite morphology |
SAM (sterile alpha motif) domain | 0.297 | INHERITED FROM: abnormal axon guidance || decreased corpus callosum size || abnormal nervous system tract morphology || abnormal axon pruning |
EF-hand modules in multidomain proteins | 0.2993 | INHERITED FROM: abnormal somatic motor system morphology |
Nuclear receptor ligand-binding domain | 0.3072 | INHERITED FROM: abnormal substantia nigra morphology || abnormal optic disc morphology || abnormal optic nerve morphology |
Ngr ectodomain-like | 0.3072 | INHERITED FROM: abnormal olfactory tract morphology || abnormal spinal cord ventral commissure morphology || abnormal olfactory cortex morphology || abnormal spinal cord commissure morphology || abnormal spinal cord lateral column morphology |
Nuclear receptor | 0.3072 | INHERITED FROM: abnormal substantia nigra morphology || abnormal optic disc morphology || abnormal optic nerve morphology |
HMG-box | 0.3102 | INHERITED FROM: abnormal sympathetic neuron morphology || abnormal sympathetic ganglion morphology || optic nerve hypoplasia || abnormal superior cervical ganglion morphology || abnormal paravertebral ganglion morphology |
NF-kappa-B/REL/DORSAL transcription factors, C-terminal domain | 0.3435 | INHERITED FROM: abnormal sensory neuron innervation pattern || abnormal trigeminal nerve morphology || abnormal spinal cord dorsal column morphology |
Integrin alpha N-terminal domain | 0.3782 | INHERITED FROM: axon degeneration |
Bromodomain | 0.3844 | INHERITED FROM: abnormal neural tube closure |
Extracellular domain of cell surface receptors | 0.3923 | INHERITED FROM: abnormal retinal ganglion cell morphology |
Spermadhesin, CUB domain | 0.4231 | INHERITED FROM: abnormal Purkinje cell innervation |
Rel/Dorsal transcription factors, DNA-binding domain | 0.4495 | INHERITED FROM: abnormal spinal cord white matter morphology || abnormal sensory neuron innervation pattern || abnormal trigeminal nerve morphology || abnormal spinal cord dorsal column morphology |
Hairy Orange domain | 0.4495 | INHERITED FROM: increased neuron number || increased sensory neuron number |
LDL receptor-like module | 0.4631 | INHERITED FROM: amyloid beta deposits |
Motor proteins | 0.5068 | INHERITED FROM: short cochlear hair cell stereocilia || decreased outer hair cell stereocilia number || decreased cochlear hair cell stereocilia number || decreased inner hair cell stereocilia number |
GAF domain | 0.5142 | INHERITED FROM: abnormal retinal photoreceptor morphology || decreased sensory neuron number || decreased retinal photoreceptor cell number || neuron degeneration || retinal photoreceptor degeneration |
Hypoxia-inducible factor Hif2a, C-terminal domain | 0.5323 | INHERITED FROM: abnormal forebrain morphology || enlarged brain ventricles || abnormal brain ventricle size |
Classic zinc finger, C2H2 | 0.5363 | INHERITED FROM: abnormal olfactory nerve morphology || abnormal brain development |
Intermediate filament protein, coiled coil region | 0.5445 | INHERITED FROM: abnormal spinal nerve morphology |
Integrin domains | 0.5818 | INHERITED FROM: abnormal sciatic nerve morphology |
Proton glutamate symport protein | 0.5887 | INHERITED FROM: abnormal neuron number || decreased neuron number |
Complement control module/SCR domain | 0.6015 | INHERITED FROM: abnormal Purkinje cell innervation |
DEP domain | 0.6342 | INHERITED FROM: abnormal orientation of cochlear hair cell stereociliary bundles || increased neuron number || abnormal cochlear hair cell stereociliary bundle morphology || abnormal hair cell morphology || craniorachischisis || abnormal cochlear hair cell morphology || abnormal cochlear outer hair cell morphology || increased cochlear hair cell number || increased sensory neuron number || abnormal cochlear hair cell number |
Adenylyl and guanylyl cyclase catalytic domain | 0.6342 | INHERITED FROM: abnormal sensory neuron morphology |
Phosphotyrosine-binding domain (PTB) | 0.6793 | INHERITED FROM: abnormal cortical marginal zone morphology || absent corpus callosum || abnormal rostral migratory stream morphology || abnormal postnatal subventricular zone morphology |
BAR domain | 0.7325 | INHERITED FROM: abnormal synaptic vesicle number || abnormal synaptic vesicle morphology |
PDEase | 0.7434 | INHERITED FROM: decreased retinal photoreceptor cell number || retinal photoreceptor degeneration |
Enabled/VASP homology 1 domain (EVH1 domain) | 0.7434 | INHERITED FROM: abnormal radial glial cell morphology || abnormal cortical intermediate zone morphology || absent brain internal capsule || abnormal brain ventricle morphology || abnormal subarachnoid space morphology || enlarged brain ventricles || abnormal cortical plate morphology || abnormal brain meninges morphology || abnormal brain ventricular system morphology || ectopic neuron || abnormal brain white matter morphology || abnormal glial cell morphology || abnormal brain pia mater morphology || abnormal brain ventricle size || hydroencephaly || abnormal neurite morphology || abnormal CNS glial cell morphology || abnormal meninges morphology || ectopic cortical neuron |
SAP domain | 0.7575 | INHERITED FROM: abnormal striatum morphology || abnormal basal ganglion morphology |
PDZ domain | 0.7858 | INHERITED FROM: abnormal cochlear hair cell stereociliary bundle morphology || craniorachischisis || abnormal cochlear outer hair cell morphology |
ABC transporter transmembrane region | 0.8165 | INHERITED FROM: amyloid beta deposits || nervous system inclusion bodies |
PLC-like (P variant) | 0.8181 | INHERITED FROM: abnormal synaptic vesicle number |
ABC transporter ATPase domain-like | 0.8501 | INHERITED FROM: nervous system inclusion bodies |
SNARE fusion complex | 0.8678 | INHERITED FROM: abnormal axon extension |
Calmodulin-like | 0.882 | INHERITED FROM: abnormal retinal cone cell morphology |
Canonical RBD | 0.9756 | INHERITED FROM: premature neuronal precursor differentiation |
cAMP-binding domain | 0.9908 | INHERITED FROM: abnormal olfactory bulb glomerular layer morphology || decreased retinal photoreceptor cell number |
Nicotinic receptor ligand binding domain-like | 1 | INHERITED FROM: abnormal hair cell morphology || abnormal cochlear hair cell morphology || cochlear ganglion degeneration || abnormal innervation || abnormal cochlear inner hair cell morphology || abnormal cochlear outer hair cell morphology || abnormal cochlear OHC efferent innervation pattern |
Synaptotagmin-like (S variant) | 1 | INHERITED FROM: abnormal synaptic vesicle number |
Neurotransmitter-gated ion-channel transmembrane pore | 1 | INHERITED FROM: abnormal hair cell morphology || abnormal cochlear hair cell morphology || cochlear ganglion degeneration || abnormal innervation || abnormal cochlear inner hair cell morphology || abnormal cochlear outer hair cell morphology || abnormal cochlear OHC efferent innervation pattern |
Rhodopsin-like | 1 | INHERITED FROM: abnormal chemoreceptor morphology || abnormal olfactory bulb development || increased thyrotroph cell number || abnormal olfactory sensory neuron morphology || abnormal olfactory neuron innervation pattern |
Voltage-gated potassium channels | 1 | INHERITED FROM: abnormal olfactory bulb glomerular layer morphology |
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 |
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 |
Homeodomain | 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 |
Sema domain | 0.00001413 | Direct |
Frizzled cysteine-rich domain | 0.00003812 | Direct |
Spectrin repeat | 0.00005865 | Direct |
Laminin-type module | 0.00009245 | Direct |
Ephrin ectodomain | 0.002174 | Inherited |
Paired domain | 0.003835 | Inherited |
Cell cycle transcription factor e2f-dp | 0.003835 | Inherited |
DIX domain | 0.005619 | Inherited |
SMAD MH1 domain | 0.008917 | Inherited |
SMAD domain | 0.008917 | Inherited |
L domain | 0.02 | Inherited |
Doublecortin (DC) | 0.02 | Inherited |
Forkhead DNA-binding domain | 0.02115 | Inherited |
Laminin G-like module | 0.02808 | Inherited |
Plexin repeat | 0.03239 | Inherited |
Formate/glycerate dehydrogenases, substrate-binding domain | 0.0343 | Inherited |
beta-glycanases | 0.0343 | Inherited |
GDNF receptor-like | 0.0343 | Inherited |
Mib/herc2 domain | 0.0343 | Inherited |
Multidrug efflux transporter AcrB transmembrane domain | 0.0343 | Inherited |
SRF-like | 0.0343 | Inherited |
HMA, heavy metal-associated domain | 0.0343 | Inherited |
Ephrin receptor ligand binding domain | 0.03672 | Inherited |
Clc chloride channel | 0.04497 | Inherited |
POU-specific domain | 0.05074 | Inherited |
Fibronectin type III | 0.05765 | Inherited |
Bcl-2 inhibitors of programmed cell death | 0.08084 | Inherited |
Cap-Gly domain | 0.08794 | Inherited |
Cadherin | 0.1009 | Inherited |
HLH, helix-loop-helix DNA-binding domain | 0.1062 | Inherited |
CBS-domain pair | 0.1102 | Inherited |
Growth factor receptor domain | 0.122 | Inherited |
SH3-domain | 0.1311 | Inherited |
Transforming growth factor (TGF)-beta | 0.158 | Inherited |
Formate/glycerate dehydrogenases, NAD-domain | 0.1643 | Inherited |
Acetylcholinesterase-like | 0.1792 | Inherited |
Cyclin | 0.1915 | Inherited |
FYVE, a phosphatidylinositol-3-phosphate binding domain | 0.2041 | Inherited |
I set domains | 0.212 | Inherited |
EGF-type module | 0.2224 | Inherited |
YWTD domain | 0.2612 | Inherited |
p120GAP domain-like | 0.2802 | Inherited |
SAM (sterile alpha motif) domain | 0.297 | Inherited |
EF-hand modules in multidomain proteins | 0.2993 | Inherited |
Nuclear receptor ligand-binding domain | 0.3072 | Inherited |
Ngr ectodomain-like | 0.3072 | Inherited |
Nuclear receptor | 0.3072 | Inherited |
HMG-box | 0.3102 | Inherited |
NF-kappa-B/REL/DORSAL transcription factors, C-terminal domain | 0.3435 | Inherited |
Integrin alpha N-terminal domain | 0.3782 | Inherited |
Bromodomain | 0.3844 | Inherited |
Extracellular domain of cell surface receptors | 0.3923 | Inherited |
Spermadhesin, CUB domain | 0.4231 | Inherited |
Rel/Dorsal transcription factors, DNA-binding domain | 0.4495 | Inherited |
Hairy Orange domain | 0.4495 | Inherited |
LDL receptor-like module | 0.4631 | Inherited |
Motor proteins | 0.5068 | Inherited |
GAF domain | 0.5142 | Inherited |
Hypoxia-inducible factor Hif2a, C-terminal domain | 0.5323 | Inherited |
Classic zinc finger, C2H2 | 0.5363 | Inherited |
Intermediate filament protein, coiled coil region | 0.5445 | Inherited |
Integrin domains | 0.5818 | Inherited |
Proton glutamate symport protein | 0.5887 | Inherited |
Complement control module/SCR domain | 0.6015 | Inherited |
DEP domain | 0.6342 | Inherited |
Adenylyl and guanylyl cyclase catalytic domain | 0.6342 | Inherited |
Phosphotyrosine-binding domain (PTB) | 0.6793 | Inherited |
BAR domain | 0.7325 | Inherited |
PDEase | 0.7434 | Inherited |
Enabled/VASP homology 1 domain (EVH1 domain) | 0.7434 | Inherited |
SAP domain | 0.7575 | Inherited |
PDZ domain | 0.7858 | Inherited |
ABC transporter transmembrane region | 0.8165 | Inherited |
PLC-like (P variant) | 0.8181 | Inherited |
ABC transporter ATPase domain-like | 0.8501 | Inherited |
SNARE fusion complex | 0.8678 | Inherited |
Calmodulin-like | 0.882 | Inherited |
Canonical RBD | 0.9756 | Inherited |
cAMP-binding domain | 0.9908 | Inherited |
Nicotinic receptor ligand binding domain-like | 1 | Inherited |
Synaptotagmin-like (S variant) | 1 | Inherited |
Neurotransmitter-gated ion-channel transmembrane pore | 1 | Inherited |
Rhodopsin-like | 1 | Inherited |
Voltage-gated potassium channels | 1 | Inherited |
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A presence/absence matrix is generated using protein domain
architecture data for all genomes in SUPERFAMILY. The PAUP
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
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]
Supra-domain (including individual superfamily)
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Supra-domains annotated to this MP term (SPMP level: Least Informative)
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 |
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 |
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 |
49899,57196 49899 - Concanavalin A-like lectins/glucanases 57196 - EGF/Laminin | 0.0000009232 | DIRECT |
49899,49899 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases | 0.000006599 | DIRECT |
101912,103575 101912 - Sema domain 103575 - Plexin repeat | 0.000007322 | DIRECT |
46966,46966 46966 - Spectrin repeat 46966 - Spectrin repeat | 0.00002309 | DIRECT |
57424,57424 57424 - LDL receptor-like module 57424 - LDL receptor-like module | 0.001966 | INHERITED FROM: amyloid beta deposits || abnormal cerebellum morphology |
57196,63825 57196 - EGF/Laminin 63825 - YWTD domain | 0.004575 | INHERITED FROM: abnormal cerebellum morphology |
57184,49265 57184 - Growth factor receptor domain 49265 - Fibronectin type III | 0.01185 | INHERITED FROM: abnormal sensory neuron morphology || abnormal innervation || abnormal sensory neuron innervation pattern |
63501,50242 63501 - Frizzled cysteine-rich domain 50242 - TIMP-like | 0.01185 | INHERITED FROM: open neural tube || craniorachischisis || spina bifida || abnormal neural tube morphology || abnormal neural tube closure |
57196,57184 57196 - EGF/Laminin 57184 - Growth factor receptor domain | 0.01289 | INHERITED FROM: abnormal cochlear hair cell number || abnormal cochlear inner hair cell number || increased cochlear inner hair cell number || abnormal cochlear inner hair cell morphology || increased neuron number || increased sensory neuron number || abnormal cochlear outer hair cell morphology || abnormal cochlear outer hair cell number || abnormal cochlear hair cell morphology |
57184,63825 57184 - Growth factor receptor domain 63825 - YWTD domain | 0.01669 | INHERITED FROM: abnormal cerebral hemisphere morphology || abnormal cerebellar cortex morphology |
52058,57184 52058 - L domain-like 57184 - Growth factor receptor domain | 0.01669 | INHERITED FROM: decreased neuron number || abnormal trigeminal nerve morphology || abnormal nervous system development || abnormal spinal cord morphology || abnormal cerebellar layer morphology || abnormal somatic sensory system morphology || abnormal cerebellar cortex morphology || abnormal somatic nervous system morphology |
57184,52058 57184 - Growth factor receptor domain 52058 - L domain-like | 0.01669 | INHERITED FROM: decreased neuron number || abnormal trigeminal nerve morphology || abnormal nervous system development || abnormal spinal cord morphology || abnormal cerebellar layer morphology || abnormal somatic sensory system morphology || abnormal cerebellar cortex morphology || abnormal somatic nervous system morphology |
89837,89837 89837 - Doublecortin (DC) 89837 - Doublecortin (DC) | 0.01669 | INHERITED FROM: abnormal dentate gyrus morphology || abnormal temporal lobe morphology || abnormal hippocampus morphology || abnormal hippocampus layer morphology |
57196,49899 57196 - EGF/Laminin 49899 - Concanavalin A-like lectins/glucanases | 0.01669 | INHERITED FROM: abnormal axon guidance || abnormal embryonic/fetal subventricular zone morphology |
103575,48726 103575 - Plexin repeat 48726 - Immunoglobulin | 0.01821 | INHERITED FROM: abnormal olfactory lobe morphology |
47413,46689 47413 - lambda repressor-like DNA-binding domains 46689 - Homeodomain-like | 0.02063 | INHERITED FROM: cochlear outer hair cell degeneration || abnormal cerebellar foliation || abnormal retinal ganglion cell morphology |
56112,47769 56112 - Protein kinase-like (PK-like) 47769 - SAM/Pointed domain | 0.02997 | INHERITED FROM: abnormal axon pruning || abnormal brain white matter morphology || abnormal innervation || abnormal axon guidance || decreased corpus callosum size || abnormal optic tract morphology || abnormal axon morphology || abnormal nervous system tract morphology |
48452,81901 48452 - TPR-like 81901 - HCP-like | 0.0301 | INHERITED FROM: abnormal telencephalon morphology || abnormal neural tube morphology |
57535,49854 57535 - Complement control module/SCR domain 49854 - Spermadhesin, CUB domain | 0.0301 | INHERITED FROM: abnormal innervation || abnormal Purkinje cell innervation |
48726,48726 48726 - Immunoglobulin 48726 - Immunoglobulin | 0.06317 | INHERITED FROM: abnormal innervation |
56112,55073 56112 - Protein kinase-like (PK-like) 55073 - Nucleotide cyclase | 0.07736 | INHERITED FROM: abnormal sensory neuron morphology || abnormal somatic sensory system morphology |
49562,48350 49562 - C2 domain (Calcium/lipid-binding domain, CaLB) 48350 - GTPase activation domain, GAP | 0.07736 | INHERITED FROM: abnormal hindbrain morphology || abnormal cerebellar layer morphology || abnormal cerebellar cortex morphology |
57196,57196 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.08244 | INHERITED FROM: short photoreceptor inner segment || abnormal cochlear hair cell number || abnormal cochlear inner hair cell number || abnormal spinal cord ventral commissure morphology || increased cochlear inner hair cell number || abnormal Muller cell morphology || abnormal Schwann cell morphology || abnormal rostral migratory stream morphology || abnormal olfactory lobe morphology || abnormal Bergmann glial cell morphology || abnormal cochlear outer hair cell number || abnormal spinal cord commissure morphology |
52058,48726 52058 - L domain-like 48726 - Immunoglobulin | 0.09527 | INHERITED FROM: abnormal telencephalon development || abnormal dorsal root ganglion morphology |
49313,49313 49313 - Cadherin-like 49313 - Cadherin-like | 0.1103 | INHERITED FROM: 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 || abnormal cochlear hair cell morphology || abnormal outer hair cell stereociliary bundle morphology |
52283,51735 52283 - Formate/glycerate dehydrogenase catalytic domain-like 51735 - NAD(P)-binding Rossmann-fold domains | 0.1489 | INHERITED FROM: abnormal embryonic neuroepithelium morphology |
81296,81296 81296 - E set domains 81296 - E set domains | 0.2208 | INHERITED FROM: ectopic cerebellar granule cells || abnormal hippocampal mossy fiber morphology || abnormal cerebellar granule cell morphology || abnormal cerebellar foliation || abnormal amacrine cell morphology |
57184,57196 57184 - Growth factor receptor domain 57196 - EGF/Laminin | 0.2208 | INHERITED FROM: abnormal cochlear hair cell number || abnormal cochlear inner hair cell number || increased cochlear inner hair cell number || increased sensory neuron number || increased cochlear hair cell number || abnormal cochlear outer hair cell number |
49854,57535 49854 - Spermadhesin, CUB domain 57535 - Complement control module/SCR domain | 0.2257 | INHERITED FROM: abnormal innervation || abnormal Purkinje cell innervation |
57716,57716 57716 - Glucocorticoid receptor-like (DNA-binding domain) 57716 - Glucocorticoid receptor-like (DNA-binding domain) | 0.2362 | INHERITED FROM: abnormal pituitary gland development || abnormal Rathke's pouch development || abnormal pituitary diverticulum morphology |
47473,47473 47473 - EF-hand 47473 - EF-hand | 0.253 | INHERITED FROM: abnormal somatic motor system morphology |
63825,57196 63825 - YWTD domain 57196 - EGF/Laminin | 0.3339 | INHERITED FROM: abnormal cerebellum morphology || abnormal metencephalon morphology || abnormal forebrain morphology |
57716,48508 57716 - Glucocorticoid receptor-like (DNA-binding domain) 48508 - Nuclear receptor ligand-binding domain | 0.3519 | INHERITED FROM: abnormal optic disc morphology || abnormal optic nerve morphology || optic disc coloboma |
69318,69179 69318 - Integrin alpha N-terminal domain 69179 - Integrin domains | 0.3956 | INHERITED FROM: axon degeneration |
69179,69179 69179 - Integrin domains 69179 - Integrin domains | 0.3956 | INHERITED FROM: axon degeneration |
49417,81296 49417 - p53-like transcription factors 81296 - E set domains | 0.44 | INHERITED FROM: abnormal trigeminal nerve morphology || abnormal sensory neuron innervation pattern || abnormal spinal cord dorsal column morphology || abnormal spinal cord white matter morphology |
47459,158457 47459 - HLH, helix-loop-helix DNA-binding domain 158457 - Orange domain-like | 0.44 | INHERITED FROM: increased neuron number || increased sensory neuron number |
57424,57184 57424 - LDL receptor-like module 57184 - Growth factor receptor domain | 0.44 | INHERITED FROM: abnormal cerebral hemisphere morphology || abnormal cerebellar cortex morphology |
57667,57667 57667 - beta-beta-alpha zinc fingers 57667 - beta-beta-alpha zinc fingers | 0.4572 | INHERITED FROM: abnormal olfactory nerve morphology |
55781,55781 55781 - GAF domain-like 55781 - GAF domain-like | 0.505 | INHERITED FROM: decreased neuron number || abnormal retinal photoreceptor morphology || decreased sensory neuron number || retinal photoreceptor degeneration || neuron degeneration || decreased retinal photoreceptor cell number |
55781,109604 55781 - GAF domain-like 109604 - HD-domain/PDEase-like | 0.505 | INHERITED FROM: decreased neuron number || abnormal retinal photoreceptor morphology || decreased sensory neuron number || retinal photoreceptor degeneration || neuron degeneration || decreased retinal photoreceptor cell number |
50044,50044 50044 - SH3-domain 50044 - SH3-domain | 0.5219 | INHERITED FROM: abnormal brain commissure morphology |
57535,57535 57535 - Complement control module/SCR domain 57535 - Complement control module/SCR domain | 0.5937 | INHERITED FROM: abnormal Purkinje cell innervation |
50156,50156 50156 - PDZ domain-like 50156 - PDZ domain-like | 0.5976 | INHERITED FROM: abnormal cochlear hair cell stereociliary bundle morphology || abnormal cochlear outer hair cell morphology || abnormal outer hair cell stereociliary bundle morphology |
90123,52540 90123 - ABC transporter transmembrane region 52540 - P-loop containing nucleoside triphosphate hydrolases | 0.7625 | INHERITED FROM: amyloid beta deposits || nervous system inclusion bodies |
55550,56112 55550 - SH2 domain 56112 - Protein kinase-like (PK-like) | 0.7757 | INHERITED FROM: delayed neural tube closure |
63712,90112 63712 - Nicotinic receptor ligand binding domain-like 90112 - Neurotransmitter-gated ion-channel transmembrane pore | 0.9999 | INHERITED FROM: abnormal cochlear OHC efferent innervation pattern || abnormal hair cell morphology || cochlear ganglion degeneration || abnormal innervation || abnormal cochlear inner hair cell morphology || abnormal cochlear outer hair cell morphology || abnormal cochlear hair cell 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 |
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 |
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 |
49899,57196 49899 - Concanavalin A-like lectins/glucanases 57196 - EGF/Laminin | 0.0000009232 | Direct |
49899,49899 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases | 0.000006599 | Direct |
101912,103575 101912 - Sema domain 103575 - Plexin repeat | 0.000007322 | Direct |
46966,46966 46966 - Spectrin repeat 46966 - Spectrin repeat | 0.00002309 | Direct |
57424,57424 57424 - LDL receptor-like module 57424 - LDL receptor-like module | 0.001966 | Inherited |
57196,63825 57196 - EGF/Laminin 63825 - YWTD domain | 0.004575 | Inherited |
57184,49265 57184 - Growth factor receptor domain 49265 - Fibronectin type III | 0.01185 | Inherited |
63501,50242 63501 - Frizzled cysteine-rich domain 50242 - TIMP-like | 0.01185 | Inherited |
57196,57184 57196 - EGF/Laminin 57184 - Growth factor receptor domain | 0.01289 | Inherited |
57184,63825 57184 - Growth factor receptor domain 63825 - YWTD domain | 0.01669 | Inherited |
52058,57184 52058 - L domain-like 57184 - Growth factor receptor domain | 0.01669 | Inherited |
57184,52058 57184 - Growth factor receptor domain 52058 - L domain-like | 0.01669 | Inherited |
89837,89837 89837 - Doublecortin (DC) 89837 - Doublecortin (DC) | 0.01669 | Inherited |
57196,49899 57196 - EGF/Laminin 49899 - Concanavalin A-like lectins/glucanases | 0.01669 | Inherited |
103575,48726 103575 - Plexin repeat 48726 - Immunoglobulin | 0.01821 | Inherited |
47413,46689 47413 - lambda repressor-like DNA-binding domains 46689 - Homeodomain-like | 0.02063 | Inherited |
56112,47769 56112 - Protein kinase-like (PK-like) 47769 - SAM/Pointed domain | 0.02997 | Inherited |
48452,81901 48452 - TPR-like 81901 - HCP-like | 0.0301 | Inherited |
57535,49854 57535 - Complement control module/SCR domain 49854 - Spermadhesin, CUB domain | 0.0301 | Inherited |
48726,48726 48726 - Immunoglobulin 48726 - Immunoglobulin | 0.06317 | Inherited |
56112,55073 56112 - Protein kinase-like (PK-like) 55073 - Nucleotide cyclase | 0.07736 | Inherited |
49562,48350 49562 - C2 domain (Calcium/lipid-binding domain, CaLB) 48350 - GTPase activation domain, GAP | 0.07736 | Inherited |
57196,57196 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.08244 | Inherited |
52058,48726 52058 - L domain-like 48726 - Immunoglobulin | 0.09527 | Inherited |
49313,49313 49313 - Cadherin-like 49313 - Cadherin-like | 0.1103 | Inherited |
52283,51735 52283 - Formate/glycerate dehydrogenase catalytic domain-like 51735 - NAD(P)-binding Rossmann-fold domains | 0.1489 | Inherited |
81296,81296 81296 - E set domains 81296 - E set domains | 0.2208 | Inherited |
57184,57196 57184 - Growth factor receptor domain 57196 - EGF/Laminin | 0.2208 | Inherited |
49854,57535 49854 - Spermadhesin, CUB domain 57535 - Complement control module/SCR domain | 0.2257 | Inherited |
57716,57716 57716 - Glucocorticoid receptor-like (DNA-binding domain) 57716 - Glucocorticoid receptor-like (DNA-binding domain) | 0.2362 | Inherited |
47473,47473 47473 - EF-hand 47473 - EF-hand | 0.253 | Inherited |
63825,57196 63825 - YWTD domain 57196 - EGF/Laminin | 0.3339 | Inherited |
57716,48508 57716 - Glucocorticoid receptor-like (DNA-binding domain) 48508 - Nuclear receptor ligand-binding domain | 0.3519 | Inherited |
69318,69179 69318 - Integrin alpha N-terminal domain 69179 - Integrin domains | 0.3956 | Inherited |
69179,69179 69179 - Integrin domains 69179 - Integrin domains | 0.3956 | Inherited |
49417,81296 49417 - p53-like transcription factors 81296 - E set domains | 0.44 | Inherited |
47459,158457 47459 - HLH, helix-loop-helix DNA-binding domain 158457 - Orange domain-like | 0.44 | Inherited |
57424,57184 57424 - LDL receptor-like module 57184 - Growth factor receptor domain | 0.44 | Inherited |
57667,57667 57667 - beta-beta-alpha zinc fingers 57667 - beta-beta-alpha zinc fingers | 0.4572 | Inherited |
55781,55781 55781 - GAF domain-like 55781 - GAF domain-like | 0.505 | Inherited |
55781,109604 55781 - GAF domain-like 109604 - HD-domain/PDEase-like | 0.505 | Inherited |
50044,50044 50044 - SH3-domain 50044 - SH3-domain | 0.5219 | Inherited |
57535,57535 57535 - Complement control module/SCR domain 57535 - Complement control module/SCR domain | 0.5937 | Inherited |
50156,50156 50156 - PDZ domain-like 50156 - PDZ domain-like | 0.5976 | Inherited |
90123,52540 90123 - ABC transporter transmembrane region 52540 - P-loop containing nucleoside triphosphate hydrolases | 0.7625 | Inherited |
55550,56112 55550 - SH2 domain 56112 - Protein kinase-like (PK-like) | 0.7757 | Inherited |
63712,90112 63712 - Nicotinic receptor ligand binding domain-like 90112 - Neurotransmitter-gated ion-channel transmembrane pore | 0.9999 | Inherited |
(show details)
Supra-domains annotated to this MP term (SPMP level: Least Informative)
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 |
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 |
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 |
46966,46966,46966 46966 - Spectrin repeat 46966 - Spectrin repeat 46966 - Spectrin repeat | 0.00006726 | DIRECT |
49899,49899,49899 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases | 0.0004752 | DIRECT |
49899,57196,57196 49899 - Concanavalin A-like lectins/glucanases 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.0006308 | DIRECT |
57196,57196,57184 57196 - EGF/Laminin 57196 - EGF/Laminin 57184 - Growth factor receptor domain | 0.0006764 | DIRECT |
81296,81296,81296 81296 - E set domains 81296 - E set domains 81296 - E set domains | 0.0006764 | DIRECT |
57424,57424,57424 57424 - LDL receptor-like module 57424 - LDL receptor-like module 57424 - LDL receptor-like module | 0.0008181 | DIRECT |
50044,50044,50044 50044 - SH3-domain 50044 - SH3-domain 50044 - SH3-domain | 0.004575 | INHERITED FROM: abnormal brain white matter morphology || abnormal brain commissure morphology || abnormal nervous system tract morphology |
57424,57184,63825 57424 - LDL receptor-like module 57184 - Growth factor receptor domain 63825 - YWTD domain | 0.004575 | INHERITED FROM: abnormal cerebral hemisphere morphology || abnormal cerebellum morphology || abnormal telencephalon morphology || abnormal cerebellar cortex morphology |
57424,57424,57184 57424 - LDL receptor-like module 57424 - LDL receptor-like module 57184 - Growth factor receptor domain | 0.004575 | INHERITED FROM: abnormal cerebral hemisphere morphology || abnormal cerebellum morphology || abnormal telencephalon morphology || abnormal cerebellar cortex morphology |
48065,50729,50044 48065 - DBL homology domain (DH-domain) 50729 - PH domain-like 50044 - SH3-domain | 0.01185 | INHERITED FROM: abnormal nervous system development |
52058,57184,52058 52058 - L domain-like 57184 - Growth factor receptor domain 52058 - L domain-like | 0.01669 | INHERITED FROM: decreased neuron number || abnormal trigeminal nerve morphology || abnormal nervous system development || abnormal spinal cord morphology || abnormal cerebellar layer morphology || abnormal somatic sensory system morphology || abnormal cerebellar cortex morphology || abnormal somatic nervous system morphology |
101912,103575,48726 101912 - Sema domain 103575 - Plexin repeat 48726 - Immunoglobulin | 0.01821 | INHERITED FROM: abnormal olfactory lobe morphology |
57535,49854,57535 57535 - Complement control module/SCR domain 49854 - Spermadhesin, CUB domain 57535 - Complement control module/SCR domain | 0.0301 | INHERITED FROM: abnormal innervation || abnormal Purkinje cell innervation |
49854,57535,49854 49854 - Spermadhesin, CUB domain 57535 - Complement control module/SCR domain 49854 - Spermadhesin, CUB domain | 0.0301 | INHERITED FROM: abnormal innervation || abnormal Purkinje cell innervation |
57196,57196,57196 57196 - EGF/Laminin 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.05414 | INHERITED FROM: short photoreceptor inner segment || abnormal cochlear hair cell number || abnormal cochlear inner hair cell number || abnormal spinal cord ventral commissure morphology || increased cochlear inner hair cell number || abnormal Muller cell morphology || abnormal photoreceptor outer segment morphology || abnormal cochlear outer hair cell number || abnormal somatic nervous system morphology || abnormal cochlear hair cell morphology || abnormal spinal cord commissure morphology |
57196,57184,57196 57196 - EGF/Laminin 57184 - Growth factor receptor domain 57196 - EGF/Laminin | 0.06219 | INHERITED FROM: abnormal cochlear hair cell number || abnormal cochlear inner hair cell number || increased cochlear inner hair cell number || 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 morphology || abnormal cochlear outer hair cell number || abnormal cochlear hair cell morphology |
48726,48726,48726 48726 - Immunoglobulin 48726 - Immunoglobulin 48726 - Immunoglobulin | 0.06478 | INHERITED FROM: abnormal brain ventricle size || enlarged brain ventricles |
48726,48726,49265 48726 - Immunoglobulin 48726 - Immunoglobulin 49265 - Fibronectin type III | 0.1103 | INHERITED FROM: abnormal brain commissure morphology || abnormal metencephalon morphology || abnormal telencephalon morphology || abnormal neuron differentiation |
49854,57535,57535 49854 - Spermadhesin, CUB domain 57535 - Complement control module/SCR domain 57535 - Complement control module/SCR domain | 0.1489 | INHERITED FROM: abnormal innervation || abnormal Purkinje cell innervation |
49313,49313,49313 49313 - Cadherin-like 49313 - Cadherin-like 49313 - Cadherin-like | 0.2003 | INHERITED FROM: 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 || abnormal cochlear hair cell morphology || abnormal outer hair cell stereociliary bundle morphology |
57184,57196,57196 57184 - Growth factor receptor domain 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.3339 | INHERITED FROM: abnormal cochlear hair cell number || abnormal cochlear inner hair cell number || increased cochlear inner hair cell number || abnormal cochlear inner hair cell morphology || increased cochlear hair cell number || abnormal cochlear outer hair cell morphology || abnormal cochlear outer hair cell number || abnormal cochlear hair cell morphology |
69179,69179,69179 69179 - Integrin domains 69179 - Integrin domains 69179 - Integrin domains | 0.3833 | 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 | 0.3956 | INHERITED FROM: abnormal Purkinje cell innervation |
69318,69179,69179 69318 - Integrin alpha N-terminal domain 69179 - Integrin domains 69179 - Integrin domains | 0.3956 | INHERITED FROM: axon degeneration |
55781,55781,109604 55781 - GAF domain-like 55781 - GAF domain-like 109604 - HD-domain/PDEase-like | 0.505 | INHERITED FROM: decreased neuron number || abnormal retinal photoreceptor morphology || decreased sensory neuron number || retinal photoreceptor degeneration || neuron degeneration || decreased retinal photoreceptor cell number |
50044,55550,56112 50044 - SH3-domain 55550 - SH2 domain 56112 - Protein kinase-like (PK-like) | 0.6285 | INHERITED FROM: ectopic neuron || delayed neural tube closure |
57667,57667,57667 57667 - beta-beta-alpha zinc fingers 57667 - beta-beta-alpha zinc fingers 57667 - beta-beta-alpha zinc fingers | 0.8135 | INHERITED FROM: 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 |
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 |
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 |
46966,46966,46966 46966 - Spectrin repeat 46966 - Spectrin repeat 46966 - Spectrin repeat | 0.00006726 | Direct |
49899,49899,49899 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases 49899 - Concanavalin A-like lectins/glucanases | 0.0004752 | Direct |
49899,57196,57196 49899 - Concanavalin A-like lectins/glucanases 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.0006308 | Direct |
57196,57196,57184 57196 - EGF/Laminin 57196 - EGF/Laminin 57184 - Growth factor receptor domain | 0.0006764 | Direct |
81296,81296,81296 81296 - E set domains 81296 - E set domains 81296 - E set domains | 0.0006764 | Direct |
57424,57424,57424 57424 - LDL receptor-like module 57424 - LDL receptor-like module 57424 - LDL receptor-like module | 0.0008181 | Direct |
50044,50044,50044 50044 - SH3-domain 50044 - SH3-domain 50044 - SH3-domain | 0.004575 | Inherited |
57424,57184,63825 57424 - LDL receptor-like module 57184 - Growth factor receptor domain 63825 - YWTD domain | 0.004575 | Inherited |
57424,57424,57184 57424 - LDL receptor-like module 57424 - LDL receptor-like module 57184 - Growth factor receptor domain | 0.004575 | Inherited |
48065,50729,50044 48065 - DBL homology domain (DH-domain) 50729 - PH domain-like 50044 - SH3-domain | 0.01185 | Inherited |
52058,57184,52058 52058 - L domain-like 57184 - Growth factor receptor domain 52058 - L domain-like | 0.01669 | Inherited |
101912,103575,48726 101912 - Sema domain 103575 - Plexin repeat 48726 - Immunoglobulin | 0.01821 | Inherited |
57535,49854,57535 57535 - Complement control module/SCR domain 49854 - Spermadhesin, CUB domain 57535 - Complement control module/SCR domain | 0.0301 | Inherited |
49854,57535,49854 49854 - Spermadhesin, CUB domain 57535 - Complement control module/SCR domain 49854 - Spermadhesin, CUB domain | 0.0301 | Inherited |
57196,57196,57196 57196 - EGF/Laminin 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.05414 | Inherited |
57196,57184,57196 57196 - EGF/Laminin 57184 - Growth factor receptor domain 57196 - EGF/Laminin | 0.06219 | Inherited |
48726,48726,48726 48726 - Immunoglobulin 48726 - Immunoglobulin 48726 - Immunoglobulin | 0.06478 | Inherited |
48726,48726,49265 48726 - Immunoglobulin 48726 - Immunoglobulin 49265 - Fibronectin type III | 0.1103 | Inherited |
49854,57535,57535 49854 - Spermadhesin, CUB domain 57535 - Complement control module/SCR domain 57535 - Complement control module/SCR domain | 0.1489 | Inherited |
49313,49313,49313 49313 - Cadherin-like 49313 - Cadherin-like 49313 - Cadherin-like | 0.2003 | Inherited |
57184,57196,57196 57184 - Growth factor receptor domain 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.3339 | Inherited |
69179,69179,69179 69179 - Integrin domains 69179 - Integrin domains 69179 - Integrin domains | 0.3833 | Inherited |
57535,57535,57535 57535 - Complement control module/SCR domain 57535 - Complement control module/SCR domain 57535 - Complement control module/SCR domain | 0.3956 | Inherited |
69318,69179,69179 69318 - Integrin alpha N-terminal domain 69179 - Integrin domains 69179 - Integrin domains | 0.3956 | Inherited |
55781,55781,109604 55781 - GAF domain-like 55781 - GAF domain-like 109604 - HD-domain/PDEase-like | 0.505 | Inherited |
50044,55550,56112 50044 - SH3-domain 55550 - SH2 domain 56112 - Protein kinase-like (PK-like) | 0.6285 | Inherited |
57667,57667,57667 57667 - beta-beta-alpha zinc fingers 57667 - beta-beta-alpha zinc fingers 57667 - beta-beta-alpha zinc fingers | 0.8135 | Inherited |
Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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A presence/absence matrix is generated using protein domains and supradomains
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