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Phenotypic Abnormality (PA): Abnormality of the neck

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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)
+ + 2:   Phenotypic abnormality [HP:0000118] <25>
+ 1:   Abnormality of head or neck [HP:0000152] <2>(87|107) (98|59|37)
0:   Abnormality of the neck [HP:0000464] <15>(4|8) (5|2|1)
- 1:   Abnormal morphology of the musculature of the neck [HP:0011006] <5>(1|1) (1|1|0)
- 1:   Limitation of neck motion [HP:0005986] <5>(1|1) (1|0|0)
- 1:   Branchial anomaly [HP:0009794] <3>(0|0) (0|0|0)
- 1:   Abnormality of neck blood vessel [HP:3000037] <2>(0|0) (0|0|0)
- 1:   Cystic hygroma [HP:0000476] <2>(2|2) (2|1|0)
- 1:   Abnormal lateral cricoarytenoid muscle morphology [HP:3000067](0|0) (0|0|0)
- 1:   Broad neck [HP:0000475](0|0) (0|0|0)
- 1:   Increased adipose tissue around the neck [HP:0000468](0|0) (0|0|0)
- 1:   Long neck [HP:0000472](0|0) (0|0|0)
- 1:   Low posterior hairline [HP:0002162](0|1) (0|0|0)
- 1:   Neck muscle hypoplasia [HP:0008984](0|0) (0|0|0)
- 1:   Redundant neck skin [HP:0005989](0|0) (0|0|0)
- 1:   Short neck [HP:0000470](0|2) (1|1|1)
- 1:   Thickened nuchal skin fold [HP:0000474](0|0) (0|0|0)
- 1:   Webbed neck [HP:0000465](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Myosin rod fragments0.07353Inherited
vWA-like0.0807Inherited
Nicotinic receptor ligand binding domain-like0.1197Inherited
Neurotransmitter-gated ion-channel transmembrane pore0.1197Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
p120GAP domain-like0.0009713Direct
T-box0.008811Inherited
Actin/HSP700.0109Inherited
Integrin A (or I) domain0.04383Inherited
Myosin rod fragments0.05664Inherited
Nicotinic receptor ligand binding domain-like0.0942Inherited
Neurotransmitter-gated ion-channel transmembrane pore0.0942Inherited
Protein kinase cysteine-rich domain (cys2, phorbol-binding domain)0.187Inherited


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)
GroEL equatorial domain-like0.0052Inherited
Myosin rod fragments0.05659Inherited
vWA-like0.06258Inherited
Nicotinic receptor ligand binding domain-like0.09588Inherited
Neurotransmitter-gated ion-channel transmembrane pore0.09588Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
53300,53300
  • 53300 - vWA-like
  • 53300 - vWA-like
  • 0.0052Inherited
    63712,90112
  • 63712 - Nicotinic receptor ligand binding domain-like
  • 90112 - Neurotransmitter-gated ion-channel transmembrane pore
  • 0.09588Inherited

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57184,57196,57184
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.0052Inherited


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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