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Mammalian Phenotype (MP): hypopigmentation

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Root: MP Hierarchy (mammalian/mouse phenotype from MGI_4.41)

Shortest distance to current term (+ for parents, - for children) MP term [MP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + 2:   mammalian phenotype [MP:0000001] <29>
+ 1:   pigmentation phenotype [MP:0001186] <13>(4|5) (6|1|3)
0:   hypopigmentation [MP:0005408] <5>(1|1) (2|0|0)
- 1:   decreased foot pigmentation [MP:0011568] <1>(0|0) (0|0|0)
- 1:   decreased ear pigmentation [MP:0011279](0|0) (0|0|0)
- 1:   decreased eye pigmentation [MP:0005172](0|0) (0|0|0)
- 1:   decreased skin pigmentation [MP:0011627](0|0) (0|0|0)
- 1:   decreased tail pigmentation [MP:0011277](0|0) (1|0|0)


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

Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
HMA, heavy metal-associated domain0.00000006163Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
HMA, heavy metal-associated domain0.000000028Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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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)
HMA, heavy metal-associated domain0.000000024Direct
WD40 repeat-like0.03894Inherited


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