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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>(86|104) (97|58|38)
+ + + + + 5:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + 4:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + + 3:   Abnormality of the mouth [HP:0000153] <2>(37|57) (46|32|22)
+ + 2:   Abnormal oral morphology [HP:0031816] <6>(35|53) (44|30|21)
+ 1:   Abnormal oral cavity morphology [HP:0000163] <14>(28|43) (36|21|15)
0:   Abnormal lip morphology [HP:0000159] <16>(5|9) (7|3|3)
- 1:   Abnormality of upper lip [HP:0000177] <7>(4|6) (5|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-like0.0009727Direct
Homeodomain-like0.007001Inherited
Notch domain0.01277Inherited
Bromodomain0.1013Inherited
SMAD/FHA domain0.5168Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Histone deacetylase, HDAC0Direct
ARID domain0.000541Direct
PHD domain0.0008314Direct
Homeodomain0.002113Inherited
Notch domain0.008429Inherited
Clathrin coat assembly domain0.05093Inherited
Bromodomain0.07631Inherited
Clathrin adaptor core protein0.07864Inherited
SPRY domain0.1304Inherited


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-like0.000516Direct
Multidrug efflux transporter AcrB transmembrane domain0.002132Inherited
Homeodomain-like0.004384Inherited
Notch domain0.008371Inherited
Bromodomain0.07967Inherited
Glycosyl hydrolase domain0.08027Inherited
SMAD/FHA domain0.4724Inherited

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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
  • 0.000516Direct
    51445,51011
  • 51445 - (Trans)glycosidases
  • 51011 - Glycosyl hydrolase domain
  • 0.08027Inherited
    57184,57581
  • 57184 - Growth factor receptor domain
  • 57581 - TB module/8-cys domain
  • 0.1333Inherited

    (show details)
    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
  • 0.1333Inherited
    57184,57184,57581
  • 57184 - Growth factor receptor domain
  • 57184 - Growth factor receptor domain
  • 57581 - TB module/8-cys domain
  • 0.1333Inherited
    57184,57196,57184
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.1333Inherited


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