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Mammalian Phenotype (MP): abnormal skeleton morphology  
(show info)
Biomedical Ontology
Like Gene Ontology (GO), biomedical ontology such as phenotype 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. Biomedical ontologies we have incorporated are as follows:
- Disease Ontology (DO) Ontology DO semantically integrates disease and medical vocabularies through extensive cross mapping of DO terms to MeSH, ICD, NCI’s thesaurus, SNOMED and OMIM.
- Human Phenotype (HP) Ontology 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 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 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 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 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 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 displays anatomical terms of the zebrafish using standard anatomical nomenclature, together with affected genes.
- Xenopus Anatomy (XA) Ontology 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 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 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.
- UniProtKB KeyWords (KW) Ontology 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).
- CTD Diseases (CD) Ontology CD is MEDIC disease vocabulary that is modified by CTD from the "Diseases" [C] branch of Medical Subject Headings (MeSH), combined with genetic disorders from the Online Mendelian Inheritance in OMIM database.
- CTD Chemicals (CC) Ontology CC is chemical vocabulary that is adapted by CTD from the "Chemicals and Drugs" category and Supplementary Concept Records of Medical Subject Headings (MeSH, a hierarchical vocabulary used to index articles for MEDLINE/PubMed).
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Root: MP Hierarchy (mammalian/mouse phenotype from MGI_4.41)
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Family( show details)
Highlighted in gray are those with FDR_all>0.001
| SCOP term |
FDR (all) |
Annotation (direct or inherited) |
| p53 DNA-binding domain-like | 0 | DIRECT |
| Nitric oxide (NO) synthase oxygenase domain | 0 | DIRECT |
| Homeodomain | 0 | DIRECT |
| RUNT domain | 0 | DIRECT |
| Clathrin adaptor appendage, alpha and beta chain-specific domain | 0 | DIRECT |
| BTG domain-like | 0 | DIRECT |
| Alpha-adaptin ear subdomain-like | 0 | DIRECT |
| p53 tetramerization domain | 0 | DIRECT |
| Retinoblastoma tumor suppressor domains | 0 | DIRECT |
| Growth factor receptor domain | 0.00004274 | DIRECT |
| VWC domain | 0.0004812 | DIRECT |
| Paired domain | 0.0004868 | DIRECT |
| Transforming growth factor (TGF)-beta | 0.0009347 | DIRECT |
| DIX domain | 0.001149 | INHERITED FROM: rib fusion || abnormal axial skeleton morphology |
| Rel/Dorsal transcription factors, DNA-binding domain | 0.001531 | INHERITED FROM: osteopetrosis || abnormal epiphyseal plate morphology || abnormal craniofacial bone morphology || abnormal jaw morphology || abnormal viscerocranium morphology || abnormal osteoclast cell number || abnormal long bone epiphyseal plate morphology || abnormal cranium morphology |
| T-box | 0.001759 | INHERITED FROM: abnormal vertebral arch morphology || rib fusion || abnormal intervertebral disk morphology || abnormal presacral vertebrae morphology || abnormal cervical atlas morphology || abnormal occipital bone morphology |
| Notch domain | 0.003937 | INHERITED FROM: abnormal axial skeleton morphology |
| Arylsulfatase | 0.00437 | INHERITED FROM: abnormal epiphyseal plate morphology || abnormal craniofacial bone morphology || abnormal long bone epiphyseal plate morphology || abnormal cranium morphology |
| Hect, E3 ligase catalytic domain | 0.009061 | INHERITED FROM: decreased bone mineral content |
| TB module/8-cys domain | 0.01178 | INHERITED FROM: abnormal jaw morphology || abnormal viscerocranium morphology || abnormal appendicular skeleton morphology || abnormal presacral vertebrae morphology || abnormal incisor morphology |
| beta-glycanases | 0.0128 | INHERITED FROM: abnormal bone structure || abnormal skeleton development |
| Cytochrome p450 reductase N-terminal domain-like | 0.0128 | INHERITED FROM: abnormal bone structure || abnormal bone mineral density || abnormal trabecular bone morphology || abnormal osteoclast cell number || increased bone mineral density || increased osteoclast cell number || abnormal osteoclast morphology || abnormal skeleton development |
| MBT repeat | 0.01355 | INHERITED FROM: abnormal vertebral column morphology || abnormal presacral vertebrae morphology || abnormal vertebrae morphology |
| TNF receptor-like | 0.01553 | INHERITED FROM: abnormal bone structure || abnormal jaw morphology |
| Fibroblast growth factors (FGF) | 0.0178 | INHERITED FROM: abnormal limb long bone morphology |
| NF-kappa-B/REL/DORSAL transcription factors, C-terminal domain | 0.02122 | INHERITED FROM: osteopetrosis || abnormal jaw morphology || abnormal viscerocranium morphology || abnormal osteoclast cell number |
| Laminin G-like module | 0.02289 | INHERITED FROM: abnormal spine curvature |
| Bromodomain | 0.02371 | INHERITED FROM: short nasal bone || decreased vertebrae number || small nasal bone |
| Transducin (alpha subunit), insertion domain | 0.03191 | INHERITED FROM: domed cranium || abnormal sternocostal joint morphology || lumbar vertebral fusion || vertebral fusion || abnormal rib morphology |
| Laminin-type module | 0.03325 | INHERITED FROM: abnormal jaw morphology || abnormal cranium morphology |
| NADPH-cytochrome p450 reductase-like | 0.0371 | INHERITED FROM: abnormal bone mineral density || abnormal trabecular bone morphology || abnormal osteoclast cell number || increased bone mineral density || increased osteoclast cell number || abnormal osteoclast morphology || abnormal skeleton development |
| NADPH-cytochrome p450 reductase FAD-binding domain-like | 0.0371 | INHERITED FROM: abnormal bone mineral density || abnormal trabecular bone morphology || abnormal osteoclast cell number || increased bone mineral density || increased osteoclast cell number || abnormal osteoclast morphology || abnormal skeleton development |
| HMG-box | 0.05161 | INHERITED FROM: abnormal sternum morphology || absent cartilage || chondrodystrophy |
| Clc chloride channel | 0.05368 | INHERITED FROM: kyphosis |
| Forkhead DNA-binding domain | 0.05561 | INHERITED FROM: abnormal jaw morphology || abnormal cranium morphology |
| YWTD domain | 0.06295 | INHERITED FROM: abnormal metacarpal bone morphology |
| Classic zinc finger, C2H2 | 0.06867 | INHERITED FROM: small clavicle || clavicle hypoplasia |
| Neutral endopeptidase (neprilysin) | 0.1168 | INHERITED FROM: small mandible || abnormal mandible morphology |
| HLH, helix-loop-helix DNA-binding domain | 0.2114 | INHERITED FROM: rib bifurcation || small clavicle || clavicle hypoplasia |
| Long-chain cytokines | 0.3011 | INHERITED FROM: abnormal osteoclast differentiation |
| Ngr ectodomain-like | 0.3377 | INHERITED FROM: osteophytes || decreased trabecular bone mass || abnormal articular cartilage morphology || abnormal tendon morphology || decreased compact bone mass |
| EF-hand modules in multidomain proteins | 0.4497 | INHERITED FROM: kyphosis |
| SAM (sterile alpha motif) domain | 0.4558 | INHERITED FROM: cervical vertebral fusion || cervical vertebral transformation |
| Nuclear receptor ligand-binding domain | 0.4625 | INHERITED FROM: abnormal basioccipital bone morphology || abnormal incus morphology || abnormal stapes morphology || split cervical axis || fusion of atlas and occipital bones || abnormal squamosal bone morphology || decreased compact bone area || increased trabecular bone volume || abnormal stapedial artery morphology || abnormal cricoid cartilage morphology || osteoporosis || fusion of vertebral arches || cervical vertebral transformation || fusion of atlas and odontoid process || abnormal odontoid process morphology || abnormal laryngeal cartilage morphology || increased bone volume || split cervical atlas |
| Nuclear receptor | 0.4625 | INHERITED FROM: abnormal basioccipital bone morphology || abnormal incus morphology || abnormal stapes morphology || split cervical axis || fusion of atlas and occipital bones || abnormal squamosal bone morphology || decreased compact bone area || abnormal cervical axis morphology || increased trabecular bone volume || abnormal stapedial artery morphology || abnormal cricoid cartilage morphology || osteoporosis || fusion of vertebral arches || cervical vertebral transformation || fusion of atlas and odontoid process || abnormal odontoid process morphology || abnormal laryngeal cartilage morphology || increased bone volume || split cervical atlas |
| TSP-1 type 1 repeat | 0.5743 | INHERITED FROM: increased compact bone thickness |
| EGF-type module | 0.5816 | INHERITED FROM: increased trabecular bone mass || abnormal tendon morphology || ectopic cartilage |
| Spermadhesin, CUB domain | 0.6001 | INHERITED FROM: abnormal tendon morphology || abnormal bone volume || abnormal osteoblast morphology || abnormal osteoblast cell number |
| DEATH domain, DD | 0.6543 | INHERITED FROM: abnormal tooth morphology |
| Nicotinic receptor ligand binding domain-like | 0.6693 | INHERITED FROM: abnormal ligament morphology || abnormal spiral ligament fibrocyte morphology || abnormal spiral ligament morphology || abnormal type IV spiral ligament fibrocytes |
| Neurotransmitter-gated ion-channel transmembrane pore | 0.6693 | INHERITED FROM: abnormal ligament morphology || abnormal spiral ligament fibrocyte morphology || abnormal spiral ligament morphology || abnormal type IV spiral ligament fibrocytes |
| Hemopexin-like domain | 0.6835 | INHERITED FROM: abnormal trabecular bone morphology || abnormal femur morphology || small maxilla |
| MMP N-terminal domain | 0.7134 | INHERITED FROM: abnormal trabecular bone morphology || abnormal femur morphology || abnormal long bone hypertrophic chondrocyte zone || decreased length of long bones || small maxilla |
| Matrix metalloproteases, catalytic domain | 0.7134 | INHERITED FROM: abnormal trabecular bone morphology || abnormal femur morphology || abnormal long bone hypertrophic chondrocyte zone || decreased length of long bones || small maxilla |
| Extracellular domain of cell surface receptors | 0.7452 | INHERITED FROM: abnormal tooth morphology || abnormal vertebral column morphology |
| G proteins | 0.7782 | INHERITED FROM: domed cranium |
| GLA-domain | 0.7784 | INHERITED FROM: abnormal trabecular bone thickness |
| Kringle modules | 0.9709 | INHERITED FROM: abnormal bone volume |
| I set domains | 1 | INHERITED FROM: axial skeleton hypoplasia |
| SCOP term |
FDR (all) |
Annotation (direct or inherited) |
| p53 DNA-binding domain-like | 0 | Direct |
| Nitric oxide (NO) synthase oxygenase domain | 0 | Direct |
| Homeodomain | 0 | Direct |
| RUNT domain | 0 | Direct |
| Clathrin adaptor appendage, alpha and beta chain-specific domain | 0 | Direct |
| BTG domain-like | 0 | Direct |
| Alpha-adaptin ear subdomain-like | 0 | Direct |
| p53 tetramerization domain | 0 | Direct |
| Retinoblastoma tumor suppressor domains | 0 | Direct |
| Growth factor receptor domain | 0.00004274 | Direct |
| VWC domain | 0.0004812 | Direct |
| Paired domain | 0.0004868 | Direct |
| Transforming growth factor (TGF)-beta | 0.0009347 | Direct |
| DIX domain | 0.001149 | Inherited |
| Rel/Dorsal transcription factors, DNA-binding domain | 0.001531 | Inherited |
| T-box | 0.001759 | Inherited |
| Notch domain | 0.003937 | Inherited |
| Arylsulfatase | 0.00437 | Inherited |
| Hect, E3 ligase catalytic domain | 0.009061 | Inherited |
| TB module/8-cys domain | 0.01178 | Inherited |
| beta-glycanases | 0.0128 | Inherited |
| Cytochrome p450 reductase N-terminal domain-like | 0.0128 | Inherited |
| MBT repeat | 0.01355 | Inherited |
| TNF receptor-like | 0.01553 | Inherited |
| Fibroblast growth factors (FGF) | 0.0178 | Inherited |
| NF-kappa-B/REL/DORSAL transcription factors, C-terminal domain | 0.02122 | Inherited |
| Laminin G-like module | 0.02289 | Inherited |
| Bromodomain | 0.02371 | Inherited |
| Transducin (alpha subunit), insertion domain | 0.03191 | Inherited |
| Laminin-type module | 0.03325 | Inherited |
| NADPH-cytochrome p450 reductase-like | 0.0371 | Inherited |
| NADPH-cytochrome p450 reductase FAD-binding domain-like | 0.0371 | Inherited |
| HMG-box | 0.05161 | Inherited |
| Clc chloride channel | 0.05368 | Inherited |
| Forkhead DNA-binding domain | 0.05561 | Inherited |
| YWTD domain | 0.06295 | Inherited |
| Classic zinc finger, C2H2 | 0.06867 | Inherited |
| Neutral endopeptidase (neprilysin) | 0.1168 | Inherited |
| HLH, helix-loop-helix DNA-binding domain | 0.2114 | Inherited |
| Long-chain cytokines | 0.3011 | Inherited |
| Ngr ectodomain-like | 0.3377 | Inherited |
| EF-hand modules in multidomain proteins | 0.4497 | Inherited |
| SAM (sterile alpha motif) domain | 0.4558 | Inherited |
| Nuclear receptor ligand-binding domain | 0.4625 | Inherited |
| Nuclear receptor | 0.4625 | Inherited |
| TSP-1 type 1 repeat | 0.5743 | Inherited |
| EGF-type module | 0.5816 | Inherited |
| Spermadhesin, CUB domain | 0.6001 | Inherited |
| DEATH domain, DD | 0.6543 | Inherited |
| Nicotinic receptor ligand binding domain-like | 0.6693 | Inherited |
| Neurotransmitter-gated ion-channel transmembrane pore | 0.6693 | Inherited |
| Hemopexin-like domain | 0.6835 | Inherited |
| MMP N-terminal domain | 0.7134 | Inherited |
| Matrix metalloproteases, catalytic domain | 0.7134 | Inherited |
| Extracellular domain of cell surface receptors | 0.7452 | Inherited |
| G proteins | 0.7782 | Inherited |
| GLA-domain | 0.7784 | Inherited |
| Kringle modules | 0.9709 | Inherited |
| I set domains | 1 | Inherited |
LINKTO: Domain2BO Download and Domain2BO Algorithm
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Supra-domain (Single)( show details)
Highlighted in gray are those with FDR>0.001
LINKTO: Supra-domain2BO Download and Supra-domain2BO Algorithm
Jump to [ Top · Hierarchy ]
Supra-domain (Duplex) in N- to C-terminal order( show details)
Highlighted in gray are those with FDR>0.001
| Supra-domain (Duplex) in N- to C-terminal order |
FDR (all) |
Annotation (direct or inherited) |
49417,47719 49417 - p53-like transcription factors 47719 - p53 tetramerization domain | 0 | DIRECT |
57184,82895 57184 - Growth factor receptor domain 82895 - TSP-1 type 1 repeat | 0 | DIRECT |
57184,57581 57184 - Growth factor receptor domain 57581 - TB module/8-cys domain | 0 | DIRECT |
49265,53300 49265 - Fibronectin type III 53300 - vWA-like | 0 | DIRECT |
57196,57424 57196 - EGF/Laminin 57424 - LDL receptor-like module | 0 | DIRECT |
57184,57184 57184 - Growth factor receptor domain 57184 - Growth factor receptor domain | 0.00003642 | DIRECT |
55550,55550 55550 - SH2 domain 55550 - SH2 domain | 0.00098 | DIRECT |
57184,57196 57184 - Growth factor receptor domain 57196 - EGF/Laminin | 0.0009828 | DIRECT |
57196,57184 57196 - EGF/Laminin 57184 - Growth factor receptor domain | 0.001059 | INHERITED FROM: abnormal phalanx morphology |
49417,81296 49417 - p53-like transcription factors 81296 - E set domains | 0.001269 | INHERITED FROM: abnormal epiphyseal plate morphology || osteopetrosis || abnormal craniofacial bone morphology || abnormal viscerocranium morphology || abnormal long bone epiphyseal plate morphology || abnormal jaw morphology || abnormal osteoclast cell number || abnormal cranium morphology |
63501,50242 63501 - Frizzled cysteine-rich domain 50242 - TIMP-like | 0.003423 | INHERITED FROM: abnormal long bone morphology || abnormal limb long bone morphology |
57603,57603 57603 - FnI-like domain 57603 - FnI-like domain | 0.004036 | INHERITED FROM: abnormal rib morphology || abnormal presacral vertebrae morphology || abnormal craniofacial bone morphology || abnormal cranium morphology || abnormal vertebrae development || abnormal intervertebral disk morphology |
57716,48508 57716 - Glucocorticoid receptor-like (DNA-binding domain) 48508 - Nuclear receptor ligand-binding domain | 0.005621 | INHERITED FROM: abnormal cervical atlas morphology || fusion of atlas and odontoid process || fusion of atlas and occipital bones || abnormal stapes morphology || abnormal odontoid process morphology || thoracic vertebral transformation || increased trabecular bone volume || abnormal incus morphology || abnormal cervical axis morphology || abnormal basioccipital bone morphology || abnormal stapedial artery morphology || abnormal laryngeal cartilage morphology || abnormal squamosal bone morphology || cervical vertebral fusion || fusion of vertebral arches || cricoid and tracheal cartilage fusion || osteoporosis || abnormal cricoid cartilage morphology || split cervical atlas || cervical vertebral transformation || split cervical axis || decreased compact bone area |
57603,82895 57603 - FnI-like domain 82895 - TSP-1 type 1 repeat | 0.0114 | INHERITED FROM: abnormal bone structure || abnormal vertebral column morphology |
53300,49265 53300 - vWA-like 49265 - Fibronectin type III | 0.0114 | INHERITED FROM: abnormal bone structure |
57196,57581 57196 - EGF/Laminin 57581 - TB module/8-cys domain | 0.01192 | INHERITED FROM: abnormal appendicular skeleton morphology || abnormal jaw morphology || abnormal bone structure || abnormal long bone morphology |
57581,57196 57581 - TB module/8-cys domain 57196 - EGF/Laminin | 0.01192 | INHERITED FROM: abnormal appendicular skeleton morphology || abnormal jaw morphology || abnormal bone structure || abnormal long bone morphology |
57196,63825 57196 - EGF/Laminin 63825 - YWTD domain | 0.01192 | INHERITED FROM: abnormal limb bone morphology || abnormal metacarpal bone morphology || abnormal craniofacial bone morphology || abnormal jaw morphology || abnormal cranium morphology || abnormal limb long bone morphology |
55785,55785 55785 - PYP-like sensor domain (PAS domain) 55785 - PYP-like sensor domain (PAS domain) | 0.02053 | INHERITED FROM: abnormal bone volume || decreased bone volume |
63825,57196 63825 - YWTD domain 57196 - EGF/Laminin | 0.02053 | INHERITED FROM: abnormal metacarpal bone morphology |
57586,57586 57586 - TNF receptor-like 57586 - TNF receptor-like | 0.02551 | INHERITED FROM: abnormal bone structure |
47473,57850 47473 - EF-hand 57850 - RING/U-box | 0.03379 | INHERITED FROM: abnormal spine curvature || kyphosis |
47895,52540 47895 - Transducin (alpha subunit), insertion domain 52540 - P-loop containing nucleoside triphosphate hydrolases | 0.05615 | INHERITED FROM: vertebral fusion || domed cranium |
49899,57196 49899 - Concanavalin A-like lectins/glucanases 57196 - EGF/Laminin | 0.05615 | INHERITED FROM: abnormal spine curvature |
48726,56436 48726 - Immunoglobulin 56436 - C-type lectin-like | 0.0666 | INHERITED FROM: abnormal limb bone morphology |
57424,57424 57424 - LDL receptor-like module 57424 - LDL receptor-like module | 0.1011 | INHERITED FROM: abnormal metacarpal bone morphology || abnormal long bone hypertrophic chondrocyte zone |
63748,63748 63748 - Tudor/PWWP/MBT 63748 - Tudor/PWWP/MBT | 0.1103 | INHERITED FROM: abnormal presacral vertebrae morphology |
47459,55785 47459 - HLH, helix-loop-helix DNA-binding domain 55785 - PYP-like sensor domain (PAS domain) | 0.1283 | INHERITED FROM: decreased bone volume |
51445,51011 51445 - (Trans)glycosidases 51011 - Glycosyl hydrolase domain | 0.2079 | INHERITED FROM: kyphosis |
47413,46689 47413 - lambda repressor-like DNA-binding domains 46689 - Homeodomain-like | 0.2249 | INHERITED FROM: abnormal temporal bone morphology |
57903,57903 57903 - FYVE/PHD zinc finger 57903 - FYVE/PHD zinc finger | 0.2629 | INHERITED FROM: vertebral transformation || thoracic vertebral transformation || abnormal thoracic vertebrae morphology || abnormal cervical vertebrae morphology |
57196,57196 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.3447 | INHERITED FROM: abnormal jaw morphology || abnormal cranium morphology |
63712,90112 63712 - Nicotinic receptor ligand binding domain-like 90112 - Neurotransmitter-gated ion-channel transmembrane pore | 0.6428 | INHERITED FROM: abnormal spiral ligament morphology || abnormal ligament morphology || abnormal type IV spiral ligament fibrocytes || abnormal spiral ligament fibrocyte morphology |
47090,55486 47090 - PGBD-like 55486 - Metalloproteases ("zincins"), catalytic domain | 0.7245 | INHERITED FROM: abnormal femur morphology || decreased length of long bones || abnormal trabecular bone morphology || small maxilla || abnormal long bone hypertrophic chondrocyte zone |
55486,50923 55486 - Metalloproteases ("zincins"), catalytic domain 50923 - Hemopexin-like domain | 0.7872 | INHERITED FROM: short femur || abnormal long bone hypertrophic chondrocyte zone |
57440,57440 57440 - Kringle-like 57440 - Kringle-like | 0.8548 | INHERITED FROM: abnormal joint morphology |
55550,56112 55550 - SH2 domain 56112 - Protein kinase-like (PK-like) | 0.958 | INHERITED FROM: abnormal bone marrow cavity morphology |
48726,48726 48726 - Immunoglobulin 48726 - Immunoglobulin | 1 | INHERITED FROM: axial skeleton hypoplasia |
| Supra-domain (Duplex) in N- to C-terminal order |
FDR (all) |
Annotation (direct or inherited) |
49417,47719 49417 - p53-like transcription factors 47719 - p53 tetramerization domain | 0 | Direct |
57184,82895 57184 - Growth factor receptor domain 82895 - TSP-1 type 1 repeat | 0 | Direct |
57184,57581 57184 - Growth factor receptor domain 57581 - TB module/8-cys domain | 0 | Direct |
49265,53300 49265 - Fibronectin type III 53300 - vWA-like | 0 | Direct |
57196,57424 57196 - EGF/Laminin 57424 - LDL receptor-like module | 0 | Direct |
57184,57184 57184 - Growth factor receptor domain 57184 - Growth factor receptor domain | 0.00003642 | Direct |
55550,55550 55550 - SH2 domain 55550 - SH2 domain | 0.00098 | Direct |
57184,57196 57184 - Growth factor receptor domain 57196 - EGF/Laminin | 0.0009828 | Direct |
57196,57184 57196 - EGF/Laminin 57184 - Growth factor receptor domain | 0.001059 | Inherited |
49417,81296 49417 - p53-like transcription factors 81296 - E set domains | 0.001269 | Inherited |
63501,50242 63501 - Frizzled cysteine-rich domain 50242 - TIMP-like | 0.003423 | Inherited |
57603,57603 57603 - FnI-like domain 57603 - FnI-like domain | 0.004036 | Inherited |
57716,48508 57716 - Glucocorticoid receptor-like (DNA-binding domain) 48508 - Nuclear receptor ligand-binding domain | 0.005621 | Inherited |
57603,82895 57603 - FnI-like domain 82895 - TSP-1 type 1 repeat | 0.0114 | Inherited |
53300,49265 53300 - vWA-like 49265 - Fibronectin type III | 0.0114 | Inherited |
57196,57581 57196 - EGF/Laminin 57581 - TB module/8-cys domain | 0.01192 | Inherited |
57581,57196 57581 - TB module/8-cys domain 57196 - EGF/Laminin | 0.01192 | Inherited |
57196,63825 57196 - EGF/Laminin 63825 - YWTD domain | 0.01192 | Inherited |
55785,55785 55785 - PYP-like sensor domain (PAS domain) 55785 - PYP-like sensor domain (PAS domain) | 0.02053 | Inherited |
63825,57196 63825 - YWTD domain 57196 - EGF/Laminin | 0.02053 | Inherited |
57586,57586 57586 - TNF receptor-like 57586 - TNF receptor-like | 0.02551 | Inherited |
47473,57850 47473 - EF-hand 57850 - RING/U-box | 0.03379 | Inherited |
47895,52540 47895 - Transducin (alpha subunit), insertion domain 52540 - P-loop containing nucleoside triphosphate hydrolases | 0.05615 | Inherited |
49899,57196 49899 - Concanavalin A-like lectins/glucanases 57196 - EGF/Laminin | 0.05615 | Inherited |
48726,56436 48726 - Immunoglobulin 56436 - C-type lectin-like | 0.0666 | Inherited |
57424,57424 57424 - LDL receptor-like module 57424 - LDL receptor-like module | 0.1011 | Inherited |
63748,63748 63748 - Tudor/PWWP/MBT 63748 - Tudor/PWWP/MBT | 0.1103 | Inherited |
47459,55785 47459 - HLH, helix-loop-helix DNA-binding domain 55785 - PYP-like sensor domain (PAS domain) | 0.1283 | Inherited |
51445,51011 51445 - (Trans)glycosidases 51011 - Glycosyl hydrolase domain | 0.2079 | Inherited |
47413,46689 47413 - lambda repressor-like DNA-binding domains 46689 - Homeodomain-like | 0.2249 | Inherited |
57903,57903 57903 - FYVE/PHD zinc finger 57903 - FYVE/PHD zinc finger | 0.2629 | Inherited |
57196,57196 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.3447 | Inherited |
63712,90112 63712 - Nicotinic receptor ligand binding domain-like 90112 - Neurotransmitter-gated ion-channel transmembrane pore | 0.6428 | Inherited |
47090,55486 47090 - PGBD-like 55486 - Metalloproteases ("zincins"), catalytic domain | 0.7245 | Inherited |
55486,50923 55486 - Metalloproteases ("zincins"), catalytic domain 50923 - Hemopexin-like domain | 0.7872 | Inherited |
57440,57440 57440 - Kringle-like 57440 - Kringle-like | 0.8548 | Inherited |
55550,56112 55550 - SH2 domain 56112 - Protein kinase-like (PK-like) | 0.958 | Inherited |
48726,48726 48726 - Immunoglobulin 48726 - Immunoglobulin | 1 | Inherited |
LINKTO: Supra-domain2BO Download and Supra-domain2BO Algorithm
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Supra-domain (Triple) in N- to C-terminal order( show details)
Highlighted in gray are those with FDR>0.001
| Supra-domain (Triple) in N- to C-terminal order |
FDR (all) |
Annotation (direct or inherited) |
63825,57196,57424 63825 - YWTD domain 57196 - EGF/Laminin 57424 - LDL receptor-like module | 0 | DIRECT |
49265,49265,53300 49265 - Fibronectin type III 49265 - Fibronectin type III 53300 - vWA-like | 0 | DIRECT |
57196,57424,57424 57196 - EGF/Laminin 57424 - LDL receptor-like module 57424 - LDL receptor-like module | 0 | DIRECT |
57184,57184,57581 57184 - Growth factor receptor domain 57184 - Growth factor receptor domain 57581 - TB module/8-cys domain | 0 | DIRECT |
57196,57184,57196 57196 - EGF/Laminin 57184 - Growth factor receptor domain 57196 - EGF/Laminin | 0.0004216 | DIRECT |
63825,57196,63825 63825 - YWTD domain 57196 - EGF/Laminin 63825 - YWTD domain | 0.00098 | DIRECT |
57184,57196,57196 57184 - Growth factor receptor domain 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.002445 | INHERITED FROM: abnormal viscerocranium morphology |
57196,57196,57184 57196 - EGF/Laminin 57196 - EGF/Laminin 57184 - Growth factor receptor domain | 0.002445 | INHERITED FROM: abnormal lumbar vertebrae morphology |
57196,57196,57581 57196 - EGF/Laminin 57196 - EGF/Laminin 57581 - TB module/8-cys domain | 0.003423 | INHERITED FROM: abnormal appendicular skeleton morphology || abnormal viscerocranium morphology || abnormal jaw morphology || abnormal bone structure || abnormal long bone morphology |
57581,57196,57196 57581 - TB module/8-cys domain 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.003423 | INHERITED FROM: abnormal appendicular skeleton morphology || abnormal viscerocranium morphology || abnormal jaw morphology || abnormal bone structure || abnormal long bone morphology |
57184,57184,57184 57184 - Growth factor receptor domain 57184 - Growth factor receptor domain 57184 - Growth factor receptor domain | 0.004036 | INHERITED FROM: abnormal appendicular skeleton morphology |
47459,55785,55785 47459 - HLH, helix-loop-helix DNA-binding domain 55785 - PYP-like sensor domain (PAS domain) 55785 - PYP-like sensor domain (PAS domain) | 0.01026 | INHERITED FROM: abnormal bone volume || decreased bone volume |
57196,57581,57184 57196 - EGF/Laminin 57581 - TB module/8-cys domain 57184 - Growth factor receptor domain | 0.0114 | INHERITED FROM: abnormal appendicular skeleton morphology || abnormal limb bone morphology || abnormal bone structure || abnormal long bone morphology || abnormal limb long bone morphology |
57196,63825,57196 57196 - EGF/Laminin 63825 - YWTD domain 57196 - EGF/Laminin | 0.01192 | INHERITED FROM: abnormal metacarpal bone morphology || abnormal vertebral column morphology || abnormal limb long bone morphology |
57603,57603,57603 57603 - FnI-like domain 57603 - FnI-like domain 57603 - FnI-like domain | 0.01192 | INHERITED FROM: abnormal rib morphology || abnormal thoracic cage morphology |
57196,57196,57196 57196 - EGF/Laminin 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.0259 | INHERITED FROM: abnormal axial skeleton morphology |
47473,47473,57850 47473 - EF-hand 47473 - EF-hand 57850 - RING/U-box | 0.03379 | INHERITED FROM: abnormal spine curvature || kyphosis |
57581,57196,57581 57581 - TB module/8-cys domain 57196 - EGF/Laminin 57581 - TB module/8-cys domain | 0.03379 | INHERITED FROM: abnormal long bone morphology |
52540,52540,52540 52540 - P-loop containing nucleoside triphosphate hydrolases 52540 - P-loop containing nucleoside triphosphate hydrolases 52540 - P-loop containing nucleoside triphosphate hydrolases | 0.04862 | INHERITED FROM: micrognathia |
48726,56436,56436 48726 - Immunoglobulin 56436 - C-type lectin-like 56436 - C-type lectin-like | 0.0666 | INHERITED FROM: abnormal limb bone morphology |
57424,57424,57424 57424 - LDL receptor-like module 57424 - LDL receptor-like module 57424 - LDL receptor-like module | 0.07696 | INHERITED FROM: abnormal metacarpal bone morphology || abnormal long bone hypertrophic chondrocyte zone |
57667,57667,57667 57667 - beta-beta-alpha zinc fingers 57667 - beta-beta-alpha zinc fingers 57667 - beta-beta-alpha zinc fingers | 0.7694 | INHERITED FROM: polyphalangy |
47090,55486,50923 47090 - PGBD-like 55486 - Metalloproteases ("zincins"), catalytic domain 50923 - Hemopexin-like domain | 0.7872 | INHERITED FROM: short femur || abnormal long bone hypertrophic chondrocyte zone |
48726,48726,48726 48726 - Immunoglobulin 48726 - Immunoglobulin 48726 - Immunoglobulin | 0.921 | INHERITED FROM: axial skeleton hypoplasia || abnormal jaw morphology || abnormal cranium morphology || short nasal bone |
48726,48726,49265 48726 - Immunoglobulin 48726 - Immunoglobulin 49265 - Fibronectin type III | 0.9328 | INHERITED FROM: micrognathia |
| Supra-domain (Triple) in N- to C-terminal order |
FDR (all) |
Annotation (direct or inherited) |
63825,57196,57424 63825 - YWTD domain 57196 - EGF/Laminin 57424 - LDL receptor-like module | 0 | Direct |
49265,49265,53300 49265 - Fibronectin type III 49265 - Fibronectin type III 53300 - vWA-like | 0 | Direct |
57196,57424,57424 57196 - EGF/Laminin 57424 - LDL receptor-like module 57424 - LDL receptor-like module | 0 | Direct |
57184,57184,57581 57184 - Growth factor receptor domain 57184 - Growth factor receptor domain 57581 - TB module/8-cys domain | 0 | Direct |
57196,57184,57196 57196 - EGF/Laminin 57184 - Growth factor receptor domain 57196 - EGF/Laminin | 0.0004216 | Direct |
63825,57196,63825 63825 - YWTD domain 57196 - EGF/Laminin 63825 - YWTD domain | 0.00098 | Direct |
57184,57196,57196 57184 - Growth factor receptor domain 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.002445 | Inherited |
57196,57196,57184 57196 - EGF/Laminin 57196 - EGF/Laminin 57184 - Growth factor receptor domain | 0.002445 | Inherited |
57196,57196,57581 57196 - EGF/Laminin 57196 - EGF/Laminin 57581 - TB module/8-cys domain | 0.003423 | Inherited |
57581,57196,57196 57581 - TB module/8-cys domain 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.003423 | Inherited |
57184,57184,57184 57184 - Growth factor receptor domain 57184 - Growth factor receptor domain 57184 - Growth factor receptor domain | 0.004036 | Inherited |
47459,55785,55785 47459 - HLH, helix-loop-helix DNA-binding domain 55785 - PYP-like sensor domain (PAS domain) 55785 - PYP-like sensor domain (PAS domain) | 0.01026 | Inherited |
57196,57581,57184 57196 - EGF/Laminin 57581 - TB module/8-cys domain 57184 - Growth factor receptor domain | 0.0114 | Inherited |
57196,63825,57196 57196 - EGF/Laminin 63825 - YWTD domain 57196 - EGF/Laminin | 0.01192 | Inherited |
57603,57603,57603 57603 - FnI-like domain 57603 - FnI-like domain 57603 - FnI-like domain | 0.01192 | Inherited |
57196,57196,57196 57196 - EGF/Laminin 57196 - EGF/Laminin 57196 - EGF/Laminin | 0.0259 | Inherited |
47473,47473,57850 47473 - EF-hand 47473 - EF-hand 57850 - RING/U-box | 0.03379 | Inherited |
57581,57196,57581 57581 - TB module/8-cys domain 57196 - EGF/Laminin 57581 - TB module/8-cys domain | 0.03379 | Inherited |
52540,52540,52540 52540 - P-loop containing nucleoside triphosphate hydrolases 52540 - P-loop containing nucleoside triphosphate hydrolases 52540 - P-loop containing nucleoside triphosphate hydrolases | 0.04862 | Inherited |
48726,56436,56436 48726 - Immunoglobulin 56436 - C-type lectin-like 56436 - C-type lectin-like | 0.0666 | Inherited |
57424,57424,57424 57424 - LDL receptor-like module 57424 - LDL receptor-like module 57424 - LDL receptor-like module | 0.07696 | Inherited |
57667,57667,57667 57667 - beta-beta-alpha zinc fingers 57667 - beta-beta-alpha zinc fingers 57667 - beta-beta-alpha zinc fingers | 0.7694 | Inherited |
47090,55486,50923 47090 - PGBD-like 55486 - Metalloproteases ("zincins"), catalytic domain 50923 - Hemopexin-like domain | 0.7872 | Inherited |
48726,48726,48726 48726 - Immunoglobulin 48726 - Immunoglobulin 48726 - Immunoglobulin | 0.921 | Inherited |
48726,48726,49265 48726 - Immunoglobulin 48726 - Immunoglobulin 49265 - Fibronectin type III | 0.9328 | Inherited |
LINKTO: Supra-domain2BO Download and Supra-domain2BO Algorithm
Plot distribution on species Tree Of Life (sTOL) for Superfamily and/or Family domains annotated by this MP term
 |
Plot tree as:
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Download Newick format tree:
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( show help)
Trees by TreeVector
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
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.
Plot distribution on species Tree Of Life (sTOL) for single supra-domains annotated by this MP term
 |
Plot tree as:
| |
Download Newick format tree:
| |
Browsing in TREE OF LIFE:
|
( show help)
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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