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Phenotypic Abnormality (PA): Abnormality of globe location

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

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 eye [HP:0000478] <2>(64|78) (69|38|28)
+ 1:   Abnormal eye morphology [HP:0012372] <12>(39|48) (41|29|22)
0:   Abnormality of globe location [HP:0100886] <6>(0|5) (1|1|0)
- 1:   Proptosis [HP:0000520] <1>(0|0) (0|0|0)
- 1:   Cyclopia [HP:0009914](0|0) (0|0|0)
- 1:   Deeply set eye [HP:0000490](0|1) (0|0|0)
- 1:   Hypertelorism [HP:0000316](0|3) (1|0|0)
- 1:   Hypotelorism [HP:0000601](0|0) (0|0|0)
- 1:   Vertical orbital dystopia [HP:0030867](0|0) (0|0|0)


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
Protein serine/threonine phosphatase0Direct
BCR-homology GTPase activation domain (BH-domain)0.01764Inherited
PWWP domain0.01864Inherited
Histone lysine methyltransferases0.03188Inherited


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)
Tudor/PWWP/MBT0.02277Inherited

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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


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