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Worm Phenotype (WP): metabolic pathway variant  
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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).
Jump to [ Top · Hierarchy · Annotations ]
Root: WP Hierarchy (worm phenotype from Wormbase Release WS226)
Jump to [ Top · Hierarchy ]
Family( show details)
Highlighted in gray are those with FDR_all>0.001
| SCOP term |
FDR (all) |
Annotation (direct or inherited) |
| Sir2 family of transcriptional regulators | 0 | DIRECT |
| Heme-dependent catalases | 0 | DIRECT |
| Histone deacetylase, HDAC | 0 | DIRECT |
| Integrin domains | 0 | DIRECT |
| Lipovitellin-phosvitin complex, superhelical domain | 0.000001116 | DIRECT |
| Lipovitellin-phosvitin complex; beta-sheet shell regions | 0.000001116 | DIRECT |
| Phoshoinositide 3-kinase (PI3K), catalytic domain | 0.0000541 | DIRECT |
| Cdc48 domain 2-like | 0.000133 | DIRECT |
| Cdc48 N-terminal domain-like | 0.000133 | DIRECT |
| Calpain large subunit, middle domain (domain III) | 0.0001696 | DIRECT |
| Proteasome subunits | 0.0009902 | DIRECT |
| Histone lysine methyltransferases | 0.0009902 | DIRECT |
| Calpain large subunit, catalytic domain (domain II) | 0.001489 | INHERITED FROM: protein degradation variant || protein metabolism variant |
| Group II chaperonin (CCT, TRIC), intermediate domain | 0.00358 | INHERITED FROM: unfolded protein response variant || protein metabolism variant |
| Spectrin repeat | 0.003644 | INHERITED FROM: protein degradation variant || protein metabolism variant |
| Pleckstrin-homology domain (PH domain) | 0.003697 | INHERITED FROM: protein degradation variant || protein phosphorylation reduced |
| Protein kinases, catalytic subunit | 0.004688 | INHERITED FROM: second messenger mediated signaling variant || protein phosphorylation variant || protein modification variant || lipid synthesis increased || protein phosphorylation reduced |
| Canonical RBD | 0.005529 | INHERITED FROM: RNA processing variant || RNA metabolism variant |
| I set domains | 0.008424 | INHERITED FROM: protein degradation variant |
| F1F0 ATP synthase subunit C | 0.01384 | INHERITED FROM: protein metabolism variant || protein transport variant |
| Group II chaperonin (CCT, TRIC), ATPase domain | 0.02115 | INHERITED FROM: unfolded protein response variant || protein metabolism variant |
| Elongation factors | 0.02382 | INHERITED FROM: proteasome core activity variant || protein phosphorylation variant || protein phosphorylation increased |
| Second domain of Mu2 adaptin subunit (ap50) of ap2 adaptor | 0.0329 | INHERITED FROM: protein metabolism variant |
| G proteins | 0.03688 | INHERITED FROM: protein phosphorylation variant || protein metabolism variant |
| Group II chaperonin (CCT, TRIC), apical domain | 0.03809 | INHERITED FROM: unfolded protein response variant || protein metabolism variant |
| LIM domain | 0.06125 | INHERITED FROM: protein degradation variant |
| Voltage-gated potassium channels | 0.07839 | INHERITED FROM: protein degradation variant |
| Cold shock DNA-binding domain-like | 0.2575 | INHERITED FROM: mRNA surveillance defective || RNA metabolism variant |
| Transducin (alpha subunit), insertion domain | 0.3708 | INHERITED FROM: protein phosphorylation variant || protein phosphorylation reduced |
| PHD domain | 0.4094 | INHERITED FROM: protein modification variant || protein methylation variant |
| Adenylyl and guanylyl cyclase catalytic domain | 0.5437 | INHERITED FROM: second messenger mediated signaling variant |
| Cytochrome P450 | 0.7798 | INHERITED FROM: metabolite content decreased |
| SCOP term |
FDR (all) |
Annotation (direct or inherited) |
| Sir2 family of transcriptional regulators | 0 | Direct |
| Heme-dependent catalases | 0 | Direct |
| Histone deacetylase, HDAC | 0 | Direct |
| Integrin domains | 0 | Direct |
| Lipovitellin-phosvitin complex, superhelical domain | 0.000001116 | Direct |
| Lipovitellin-phosvitin complex; beta-sheet shell regions | 0.000001116 | Direct |
| Phoshoinositide 3-kinase (PI3K), catalytic domain | 0.0000541 | Direct |
| Cdc48 domain 2-like | 0.000133 | Direct |
| Cdc48 N-terminal domain-like | 0.000133 | Direct |
| Calpain large subunit, middle domain (domain III) | 0.0001696 | Direct |
| Proteasome subunits | 0.0009902 | Direct |
| Histone lysine methyltransferases | 0.0009902 | Direct |
| Calpain large subunit, catalytic domain (domain II) | 0.001489 | Inherited |
| Group II chaperonin (CCT, TRIC), intermediate domain | 0.00358 | Inherited |
| Spectrin repeat | 0.003644 | Inherited |
| Pleckstrin-homology domain (PH domain) | 0.003697 | Inherited |
| Protein kinases, catalytic subunit | 0.004688 | Inherited |
| Canonical RBD | 0.005529 | Inherited |
| I set domains | 0.008424 | Inherited |
| F1F0 ATP synthase subunit C | 0.01384 | Inherited |
| Group II chaperonin (CCT, TRIC), ATPase domain | 0.02115 | Inherited |
| Elongation factors | 0.02382 | Inherited |
| Second domain of Mu2 adaptin subunit (ap50) of ap2 adaptor | 0.0329 | Inherited |
| G proteins | 0.03688 | Inherited |
| Group II chaperonin (CCT, TRIC), apical domain | 0.03809 | Inherited |
| LIM domain | 0.06125 | Inherited |
| Voltage-gated potassium channels | 0.07839 | Inherited |
| Cold shock DNA-binding domain-like | 0.2575 | Inherited |
| Transducin (alpha subunit), insertion domain | 0.3708 | Inherited |
| PHD domain | 0.4094 | Inherited |
| Adenylyl and guanylyl cyclase catalytic domain | 0.5437 | Inherited |
| Cytochrome P450 | 0.7798 | 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) |
50692,54585 50692 - ADC-like 54585 - Cdc48 domain 2-like | 0 | DIRECT |
54585,52540 54585 - Cdc48 domain 2-like 52540 - P-loop containing nucleoside triphosphate hydrolases | 0 | DIRECT |
56968,48431 56968 - Lipovitellin-phosvitin complex; beta-sheet shell regions 48431 - Lipovitellin-phosvitin complex, superhelical domain | 0.0000003774 | DIRECT |
48431,56968 48431 - Lipovitellin-phosvitin complex, superhelical domain 56968 - Lipovitellin-phosvitin complex; beta-sheet shell regions | 0.0000003774 | DIRECT |
54001,49758 54001 - Cysteine proteinases 49758 - Calpain large subunit, middle domain (domain III) | 0.0001477 | DIRECT |
81333,81333 81333 - F1F0 ATP synthase subunit C 81333 - F1F0 ATP synthase subunit C | 0.003327 | INHERITED FROM: protein metabolism variant || protein transport variant |
48592,54849 48592 - GroEL equatorial domain-like 54849 - GroEL-intermediate domain like | 0.005993 | INHERITED FROM: protein metabolism variant || unfolded protein response variant |
54849,52029 54849 - GroEL-intermediate domain like 52029 - GroEL apical domain-like | 0.005993 | INHERITED FROM: protein metabolism variant || unfolded protein response variant |
48065,50729 48065 - DBL homology domain (DH-domain) 50729 - PH domain-like | 0.009014 | INHERITED FROM: protein metabolism variant |
48726,49265 48726 - Immunoglobulin 49265 - Fibronectin type III | 0.01118 | INHERITED FROM: protein degradation variant |
46966,46966 46966 - Spectrin repeat 46966 - Spectrin repeat | 0.01279 | INHERITED FROM: protein degradation variant || protein metabolism variant |
52540,50447 52540 - P-loop containing nucleoside triphosphate hydrolases 50447 - Translation proteins | 0.02097 | INHERITED FROM: proteasome core activity variant || protein phosphorylation increased || protein phosphorylation variant |
48726,48726 48726 - Immunoglobulin 48726 - Immunoglobulin | 0.08633 | INHERITED FROM: protein degradation variant |
47954,47954 47954 - Cyclin-like 47954 - Cyclin-like | 0.1141 | INHERITED FROM: protein phosphorylation variant || protein phosphorylation reduced |
47895,52540 47895 - Transducin (alpha subunit), insertion domain 52540 - P-loop containing nucleoside triphosphate hydrolases | 0.348 | INHERITED FROM: protein phosphorylation variant || protein phosphorylation reduced |
| Supra-domain (Duplex) in N- to C-terminal order |
FDR (all) |
Annotation (direct or inherited) |
50692,54585 50692 - ADC-like 54585 - Cdc48 domain 2-like | 0 | Direct |
54585,52540 54585 - Cdc48 domain 2-like 52540 - P-loop containing nucleoside triphosphate hydrolases | 0 | Direct |
56968,48431 56968 - Lipovitellin-phosvitin complex; beta-sheet shell regions 48431 - Lipovitellin-phosvitin complex, superhelical domain | 0.0000003774 | Direct |
48431,56968 48431 - Lipovitellin-phosvitin complex, superhelical domain 56968 - Lipovitellin-phosvitin complex; beta-sheet shell regions | 0.0000003774 | Direct |
54001,49758 54001 - Cysteine proteinases 49758 - Calpain large subunit, middle domain (domain III) | 0.0001477 | Direct |
81333,81333 81333 - F1F0 ATP synthase subunit C 81333 - F1F0 ATP synthase subunit C | 0.003327 | Inherited |
48592,54849 48592 - GroEL equatorial domain-like 54849 - GroEL-intermediate domain like | 0.005993 | Inherited |
54849,52029 54849 - GroEL-intermediate domain like 52029 - GroEL apical domain-like | 0.005993 | Inherited |
48065,50729 48065 - DBL homology domain (DH-domain) 50729 - PH domain-like | 0.009014 | Inherited |
48726,49265 48726 - Immunoglobulin 49265 - Fibronectin type III | 0.01118 | Inherited |
46966,46966 46966 - Spectrin repeat 46966 - Spectrin repeat | 0.01279 | Inherited |
52540,50447 52540 - P-loop containing nucleoside triphosphate hydrolases 50447 - Translation proteins | 0.02097 | Inherited |
48726,48726 48726 - Immunoglobulin 48726 - Immunoglobulin | 0.08633 | Inherited |
47954,47954 47954 - Cyclin-like 47954 - Cyclin-like | 0.1141 | Inherited |
47895,52540 47895 - Transducin (alpha subunit), insertion domain 52540 - P-loop containing nucleoside triphosphate hydrolases | 0.348 | Inherited |
LINKTO: Supra-domain2BO Download and Supra-domain2BO Algorithm
Jump to [ Top · Hierarchy ]
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) |
54585,52540,52540 54585 - Cdc48 domain 2-like 52540 - P-loop containing nucleoside triphosphate hydrolases 52540 - P-loop containing nucleoside triphosphate hydrolases | 0 | DIRECT |
50692,54585,52540 50692 - ADC-like 54585 - Cdc48 domain 2-like 52540 - P-loop containing nucleoside triphosphate hydrolases | 0 | DIRECT |
48371,48371,48371 48371 - ARM repeat 48371 - ARM repeat 48371 - ARM repeat | 0 | DIRECT |
56968,48431,56968 56968 - Lipovitellin-phosvitin complex; beta-sheet shell regions 48431 - Lipovitellin-phosvitin complex, superhelical domain 56968 - Lipovitellin-phosvitin complex; beta-sheet shell regions | 0.0000003774 | DIRECT |
48592,54849,52029 48592 - GroEL equatorial domain-like 54849 - GroEL-intermediate domain like 52029 - GroEL apical domain-like | 0.005993 | INHERITED FROM: protein metabolism variant || unfolded protein response variant |
46966,46966,46966 46966 - Spectrin repeat 46966 - Spectrin repeat 46966 - Spectrin repeat | 0.01279 | INHERITED FROM: protein degradation variant || protein metabolism variant |
48726,48726,49265 48726 - Immunoglobulin 48726 - Immunoglobulin 49265 - Fibronectin type III | 0.01279 | INHERITED FROM: protein degradation variant |
48726,48726,48726 48726 - Immunoglobulin 48726 - Immunoglobulin 48726 - Immunoglobulin | 0.05271 | INHERITED FROM: protein degradation variant |
57716,57716,57716 57716 - Glucocorticoid receptor-like (DNA-binding domain) 57716 - Glucocorticoid receptor-like (DNA-binding domain) 57716 - Glucocorticoid receptor-like (DNA-binding domain) | 0.09115 | INHERITED FROM: protein degradation variant |
| Supra-domain (Triple) in N- to C-terminal order |
FDR (all) |
Annotation (direct or inherited) |
54585,52540,52540 54585 - Cdc48 domain 2-like 52540 - P-loop containing nucleoside triphosphate hydrolases 52540 - P-loop containing nucleoside triphosphate hydrolases | 0 | Direct |
50692,54585,52540 50692 - ADC-like 54585 - Cdc48 domain 2-like 52540 - P-loop containing nucleoside triphosphate hydrolases | 0 | Direct |
48371,48371,48371 48371 - ARM repeat 48371 - ARM repeat 48371 - ARM repeat | 0 | Direct |
56968,48431,56968 56968 - Lipovitellin-phosvitin complex; beta-sheet shell regions 48431 - Lipovitellin-phosvitin complex, superhelical domain 56968 - Lipovitellin-phosvitin complex; beta-sheet shell regions | 0.0000003774 | Direct |
48592,54849,52029 48592 - GroEL equatorial domain-like 54849 - GroEL-intermediate domain like 52029 - GroEL apical domain-like | 0.005993 | Inherited |
46966,46966,46966 46966 - Spectrin repeat 46966 - Spectrin repeat 46966 - Spectrin repeat | 0.01279 | Inherited |
48726,48726,49265 48726 - Immunoglobulin 48726 - Immunoglobulin 49265 - Fibronectin type III | 0.01279 | Inherited |
48726,48726,48726 48726 - Immunoglobulin 48726 - Immunoglobulin 48726 - Immunoglobulin | 0.05271 | Inherited |
57716,57716,57716 57716 - Glucocorticoid receptor-like (DNA-binding domain) 57716 - Glucocorticoid receptor-like (DNA-binding domain) 57716 - Glucocorticoid receptor-like (DNA-binding domain) | 0.09115 | 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 WP term
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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 WP term
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Plot tree as:
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Download Newick format tree:
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Browsing in TREE OF LIFE:
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( 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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