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Phenotypic Abnormality (PA): Abnormality of the pinna

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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)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the ear [HP:0000598] <2>(18|32) (22|13|10)
+ + 2:   Abnormal ear morphology [HP:0031703] <5>(15|26) (18|11|10)
+ 1:   Abnormality of the outer ear [HP:0000356] <14>(6|7) (7|3|1)
0:   Abnormality of the pinna [HP:0000377] <28>(3|3) (3|2|0)
- 1:   Abnormality of the helix [HP:0011039] <15>(0|0) (0|0|0)
- 1:   Abnormality of earlobe [HP:0000363] <10>(0|0) (0|0|0)
- 1:   Abnormality of the antihelix [HP:0009738] <9>(0|0) (0|0|0)
- 1:   Abnormality of the antitragus [HP:0009896] <5>(0|0) (0|0|0)
- 1:   Abnormality of the tragus [HP:0009912] <4>(0|0) (0|0|0)
- 1:   Asymmetry of the ears [HP:0010722] <3>(0|0) (0|0|0)
- 1:   Microtia [HP:0008551] <3>(0|0) (0|0|0)
- 1:   Cryptotia [HP:0011252] <2>(0|0) (0|0|0)
- 1:   Macrotia [HP:0000400] <1>(0|0) (0|1|0)
- 1:   Abnormal number of tubercles [HP:0040112](0|0) (0|0|0)
- 1:   Auricular pit [HP:0030025](0|0) (0|0|0)
- 1:   Auricular tag [HP:0030021](0|0) (0|0|0)
- 1:   Calcification of the auricular cartilage [HP:0005103](0|0) (0|0|0)
- 1:   Chondritis of pinna [HP:0200047](0|0) (0|0|0)
- 1:   Crumpled ear [HP:0009901](0|0) (0|0|0)
- 1:   Cupped ear [HP:0000378](0|0) (0|0|0)
- 1:   Cystic lesions of the pinnae [HP:0010723](0|0) (0|0|0)
- 1:   Hypoplasia of the ear cartilage [HP:0100720](0|0) (0|0|0)
- 1:   Long ear [HP:0400004](0|0) (0|0|0)
- 1:   Lop ear [HP:0000394](0|0) (0|0|0)
- 1:   Mozart ear [HP:0030677](0|0) (0|0|0)
- 1:   Protruding ear [HP:0000411](1|1) (1|1|0)
- 1:   Quelprud nodule [HP:0030023](0|0) (0|0|0)
- 1:   Question mark ear [HP:0030022](0|0) (0|0|0)
- 1:   Round ear [HP:0100830](0|0) (0|0|0)
- 1:   Satyr ear [HP:0030676](0|0) (0|0|0)
- 1:   Short ear [HP:0400005](0|0) (0|0|0)
- 1:   Thickened ears [HP:0009894](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Bromodomain0.0001357Direct
SET domain0.0002629Direct
MIR domain0.04121Inherited


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Histone lysine methyltransferases0.00003718Direct
Bromodomain0.00006329Direct
MIR domain0.02918Inherited


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)
Bromodomain0.00006576Direct
SET domain0.0001327Direct
MIR domain0.03Inherited

(show details)
Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
53300,53300
  • 53300 - vWA-like
  • 53300 - vWA-like
  • 0.008045Inherited
    57903,57903
  • 57903 - FYVE/PHD zinc finger
  • 57903 - FYVE/PHD zinc finger
  • 0.2739Inherited


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