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Phenotypic Abnormality (PA): Abnormal lip morphology

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term (+ for parents, - for children) HP term [HP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + + + + 7:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + 6:   Abnormality of head or neck [HP:0000152] <2>(87|107) (98|59|37)
+ + + + + 5:   Abnormality of the head [HP:0000234] <6>(86|105) (97|58|37)
+ + + + 4:   Abnormality of the face [HP:0000271] <14>(72|88) (83|47|30)
+ + + 3:   Abnormality of the mouth [HP:0000153] <2>(38|55) (44|30|22)
+ + 2:   Abnormal oral morphology [HP:0031816] <6>(36|50) (42|28|21)
+ 1:   Abnormal oral cavity morphology [HP:0000163] <14>(29|42) (35|21|15)
0:   Abnormal lip morphology [HP:0000159] <16>(5|9) (7|3|3)
- 1:   Abnormality of upper lip [HP:0000177] <7>(4|7) (6|2|3)
- 1:   Abnormality of lower lip [HP:0000178] <6>(1|1) (2|1|0)
- 1:   Vascular malformation of the lip [HP:0031486] <4>(0|0) (0|0|0)
- 1:   Abnormal lip pigmentation [HP:0032453] <3>(0|0) (0|0|0)
- 1:   Eclabion [HP:0012472] <2>(0|0) (0|0|0)
- 1:   Lip pit [HP:0100267] <2>(0|0) (0|0|0)
- 1:   Thick vermilion border [HP:0012471] <2>(1|1) (1|0|0)
- 1:   Thin vermilion border [HP:0000233] <2>(0|1) (0|1|0)
- 1:   Cheilitis [HP:0100825] <1>(0|0) (0|0|0)
- 1:   Chapped lip [HP:0040181](0|0) (0|0|0)
- 1:   Fused lips [HP:0100788](0|0) (0|0|0)
- 1:   Lip fissure [HP:0031250](0|0) (0|0|0)
- 1:   Lip freckle [HP:0010798](0|0) (0|0|0)
- 1:   Lip telangiectasia [HP:0000214](0|0) (0|0|0)
- 1:   Neoplasm of the lip [HP:0100604](0|0) (0|0|0)
- 1:   Swollen lip [HP:0031244](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
ARID-like0.0008542Direct
Homeodomain-like0.009478Inherited
Notch domain0.0118Inherited
Bromodomain0.09629Inherited
SMAD/FHA domain0.5046Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Histone deacetylase, HDAC0Direct
ARID domain0.0004922Direct
PHD domain0.0007875Direct
Homeodomain0.003699Inherited
Notch domain0.007964Inherited
Clathrin coat assembly domain0.04855Inherited
Bromodomain0.07457Inherited
Clathrin adaptor core protein0.07728Inherited
SPRY domain0.1292Inherited


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

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
ARID-like0.0004588Direct
Multidrug efflux transporter AcrB transmembrane domain0.001936Inherited
Homeodomain-like0.006157Inherited
Notch domain0.007783Inherited
Bromodomain0.07582Inherited
Glycosyl hydrolase domain0.07769Inherited
SMAD/FHA domain0.4612Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57903,57903
  • 57903 - FYVE/PHD zinc finger
  • 57903 - FYVE/PHD zinc finger
  • 0.0004588Direct
    51445,51011
  • 51445 - (Trans)glycosidases
  • 51011 - Glycosyl hydrolase domain
  • 0.07769Inherited
    57184,57581
  • 57184 - Growth factor receptor domain
  • 57581 - TB module/8-cys domain
  • 0.1299Inherited

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57184,57581,57196
  • 57184 - Growth factor receptor domain
  • 57581 - TB module/8-cys domain
  • 57196 - EGF/Laminin
  • 0.1299Inherited
    57184,57184,57581
  • 57184 - Growth factor receptor domain
  • 57184 - Growth factor receptor domain
  • 57581 - TB module/8-cys domain
  • 0.1299Inherited
    57184,57196,57184
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.1299Inherited


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