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Disease Ontology (DO): intestinal disease

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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Root: DO Hierarchy (disease ontology from University of Maryland)

Shortest distance to current term (+ for parents, - for children) DO term [DO ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + 3:   disease [DOID:4] <8>
+ + 2:   disease of anatomical entity [DOID:7] <12>(143|187) (147|103|58)
+ 1:   gastrointestinal system disease [DOID:77] <14>(33|43) (35|18|5)
0:   intestinal disease [DOID:5295] <32>(11|13) (12|7|2)
- 1:   inflammatory bowel disease [DOID:0050589] <30>(8|11) (9|7|2)
- 1:   colonic disease [DOID:5353] <6>(1|1) (1|0|0)
- 1:   intestinal obstruction [DOID:8437] <6>(0|0) (0|0|0)
- 1:   rectal disease [DOID:1285] <6>(0|0) (0|0|0)
- 1:   duodenal disease [DOID:4072] <2>(0|0) (0|0|0)
- 1:   postgastrectomy syndrome [DOID:8439] <2>(0|0) (0|0|0)
- 1:   bowel dysfunction [DOID:9779] <1>(1|1) (1|0|0)
- 1:   cecal disease [DOID:1518] <1>(0|0) (0|0|0)
- 1:   diverticulitis [DOID:7475] <1>(0|0) (0|0|0)
- 1:   intestinal infectious disease [DOID:100] <1>(0|0) (0|0|0)
- 1:   intestinal perforation [DOID:2074] <1>(0|0) (0|0|0)
- 1:   Peutz-Jeghers syndrome [DOID:3852](1|0) (1|0|0)
- 1:   Whipple disease [DOID:8476](0|0) (0|0|0)
- 1:   acute vascular insufficiency of intestine [DOID:8590](0|0) (0|0|0)
- 1:   angiodysplasia of intestine [DOID:10846](0|0) (0|0|0)
- 1:   blind loop syndrome [DOID:10606](0|0) (0|0|0)
- 1:   chronic intestinal vascular insufficiency [DOID:8633](0|0) (0|0|0)
- 1:   duodenitis [DOID:8643](0|0) (0|0|0)
- 1:   endometriosis of intestine [DOID:11428](0|0) (0|0|0)
- 1:   inguinal hernia [DOID:0060320](0|0) (0|0|0)
- 1:   intestinal atresia [DOID:10486](0|0) (0|0|0)
- 1:   intestinal disaccharidase deficiency [DOID:9868](0|0) (0|0|0)
- 1:   mucocele of appendix [DOID:13248](0|0) (0|0|0)
- 1:   neurogenic bowel [DOID:13419](0|0) (0|0|0)
- 1:   pneumatosis cystoides intestinalis [DOID:13249](0|0) (0|0|0)
- 1:   protein-losing enteropathy [DOID:10611](0|0) (0|0|0)
- 1:   short bowel syndrome [DOID:10605](0|0) (0|0|0)
- 1:   sitosterolemia [DOID:0090019](0|0) (0|0|0)
- 1:   small intestine diverticulitis [DOID:11223](0|0) (0|0|0)
- 1:   steatorrhea [DOID:10602](0|0) (0|0|0)
- 1:   tropical sprue [DOID:10607](0|0) (0|0|0)
- 1:   umbilical hernia [DOID:0060321](0|0) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Transcription factor STAT-4 N-domain0.000002631Direct
STAT0.000002631Direct
p53-like transcription factors0.0006925Direct
DEATH domain0.002001Inherited
RNI-like0.003444Inherited
Cystine-knot cytokines0.02041Inherited
Interleukin 8-like chemokines0.05284Inherited
Aquaporin-like0.06448Inherited
4-helical cytokines0.09468Inherited
Toll/Interleukin receptor TIR domain0.1152Inherited
ARM repeat0.5913Inherited


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
STAT0.000001957Direct
Transcription factor STAT-4 N-domain0.000001957Direct
STAT DNA-binding domain0.000001957Direct
Pyrin domain, PYD0.0007087Direct
28-residue LRR0.00136Inherited
Caspase recruitment domain, CARD0.01582Inherited
Interleukin 8-like chemokines0.04041Inherited
Transforming growth factor (TGF)-beta0.0417Inherited
Aquaporin-like0.0501Inherited
Integrin A (or I) domain0.05479Inherited
Toll/Interleukin receptor TIR domain0.0926Inherited
Short-chain cytokines0.157Inherited
TNF receptor-like0.2248Inherited


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

(show details)
Supra-domain (Single) FDR (all) Annotation (direct or inherited)
STAT0.000001397Direct
Transcription factor STAT-4 N-domain0.000001397Direct
p53-like transcription factors0.0004254Direct
DEATH domain0.0013Inherited
RNI-like0.002296Inherited
Cystine-knot cytokines0.01479Inherited
Interleukin 8-like chemokines0.04028Inherited
Aquaporin-like0.04978Inherited
4-helical cytokines0.07498Inherited
Toll/Interleukin receptor TIR domain0.09205Inherited
Flavoproteins0.1028Inherited
ARM repeat0.5251Inherited

(show details)
Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
48092,47655
  • 48092 - Transcription factor STAT-4 N-domain
  • 47655 - STAT
  • 0.000001397Direct
    49417,55550
  • 49417 - p53-like transcription factors
  • 55550 - SH2 domain
  • 0.000001397Direct
    47655,49417
  • 47655 - STAT
  • 49417 - p53-like transcription factors
  • 0.000001397Direct
    49417,81296
  • 49417 - p53-like transcription factors
  • 81296 - E set domains
  • 0.004707Inherited
    57440,57440
  • 57440 - Kringle-like
  • 57440 - Kringle-like
  • 0.1034Inherited
    57586,57586
  • 57586 - TNF receptor-like
  • 57586 - TNF receptor-like
  • 0.1551Inherited
    54452,48726
  • 54452 - MHC antigen-recognition domain
  • 48726 - Immunoglobulin
  • 0.3221Inherited

    (show details)
    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    48092,47655,49417
  • 48092 - Transcription factor STAT-4 N-domain
  • 47655 - STAT
  • 49417 - p53-like transcription factors
  • 0.000001397Direct
    47655,49417,55550
  • 47655 - STAT
  • 49417 - p53-like transcription factors
  • 55550 - SH2 domain
  • 0.000001397Direct


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
    Plot tree as:   Download Newick format tree:
    (show help)