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Phenotypic Abnormality (PA): Truncal ataxia

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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)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + 4:   Abnormality of nervous system physiology [HP:0012638] <26>(101|119) (112|81|39)
+ + + 3:   Abnormality of central motor function [HP:0011442] <10>(22|26) (30|16|7)
+ + 2:   Abnormality of coordination [HP:0011443] <5>(2|3) (7|5|2)
+ 1:   Ataxia [HP:0001251] <11>(2|2) (7|4|2)
0:   Truncal ataxia [HP:0002078] <1>(0|0) (3|2|1)
- 1:   Progressive truncal ataxia [HP:0007221](0|0) (0|0|0)


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Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Metal cation-transporting ATPase, ATP-binding domain N0.0008436Direct
Calcium ATPase, transduction domain A0.0008436Direct
Calcium ATPase, transmembrane domain M0.0008436Direct

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
81660,56784
  • 81660 - Metal cation-transporting ATPase, ATP-binding domain N
  • 56784 - HAD-like
  • 0.0008436Direct
    56784,81665
  • 56784 - HAD-like
  • 81665 - Calcium ATPase, transmembrane domain M
  • 0.0008436Direct

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    81660,56784,81665
  • 81660 - Metal cation-transporting ATPase, ATP-binding domain N
  • 56784 - HAD-like
  • 81665 - Calcium ATPase, transmembrane domain M
  • 0.0008436Direct


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