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Phenotypic Abnormality (PA): Abnormality of the outer ear

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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)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of the ear [HP:0000598] <2>(18|32) (22|13|10)
+ 1:   Abnormal ear morphology [HP:0031703] <5>(15|26) (18|11|10)
0:   Abnormality of the outer ear [HP:0000356] <14>(6|7) (7|3|1)
- 1:   Abnormality of the pinna [HP:0000377] <28>(3|3) (3|2|0)
- 1:   Abnormal location of ears [HP:0000357] <6>(3|2) (3|1|0)
- 1:   Abnormality of the auditory canal [HP:0000372] <5>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia of the external ear [HP:0008772] <3>(0|0) (0|0|0)
- 1:   Neoplasm of the outer ear [HP:0040095] <3>(0|0) (0|0|0)
- 1:   Abnormality of cartilage of external ear [HP:3000022] <2>(0|0) (0|0|0)
- 1:   Abnormality of the tympanic membrane [HP:0040090](0|0) (0|0|0)
- 1:   Bilateral external ear deformity [HP:0040111](0|0) (0|0|0)
- 1:   External ear malformation [HP:0008572](0|0) (0|0|0)
- 1:   Extra concha fold [HP:0400002](0|0) (0|0|0)
- 1:   Hypertrophic auricular cartilage [HP:0008608](0|0) (0|0|0)
- 1:   Polyotia [HP:0100687](0|0) (0|0|0)
- 1:   Telangiectasia of the ear [HP:0009893](0|0) (0|0|0)
- 1:   Unilateral external ear deformity [HP:0008605](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
RuvA domain 2-like0Direct
Bromodomain0.004095Inherited
GroEL equatorial domain-like0.04204Inherited
Acyl-CoA N-acyltransferases (Nat)0.04204Inherited
SET domain0.07189Inherited
MIR domain0.2298Inherited


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
XPF/Rad1/Mus81 nuclease0Direct
VWC domain0.0001826Direct
ARID domain0.0007405Direct
Histone lysine methyltransferases0.0008925Direct
G proteins0.002093Inherited
Bromodomain0.002381Inherited
MIR domain0.1953Inherited


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)
RuvA domain 2-like0Direct
ARID-like0.000748Direct
Bromodomain0.002486Inherited
GroEL equatorial domain-like0.03067Inherited
Acyl-CoA N-acyltransferases (Nat)0.03067Inherited
SET domain0.05517Inherited
MIR domain0.1953Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
52980,47781
  • 52980 - Restriction endonuclease-like
  • 47781 - RuvA domain 2-like
  • 0Direct
    57903,57903
  • 57903 - FYVE/PHD zinc finger
  • 57903 - FYVE/PHD zinc finger
  • 0.01053Inherited
    53300,53300
  • 53300 - vWA-like
  • 53300 - vWA-like
  • 0.1953Inherited

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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
  • 0Direct


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