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Mammalian Phenotype (MP): abnormal skin development

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

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)
+ + + 3:   mammalian phenotype [MP:0000001] <29>
+ + 2:   integument phenotype [MP:0010771] <5>(46|64) (53|34|18)
+ 1:   abnormal skin morphology [MP:0002060] <16>(19|26) (24|13|8)
0:   abnormal skin development [MP:0003941] <4>(0|1) (1|0|0)
- 1:   abnormal epidermal stem cell morphology [MP:0011004] <2>(0|0) (0|0|0)
- 1:   abnormal dermatome morphology [MP:0003940] <1>(0|0) (0|0|0)
- 1:   delayed skin barrier formation [MP:0009441](0|0) (0|0|0)
- 1:   fetal bleb [MP:0008856](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)
VWC domain0.0005561Direct


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)
FnI-like domain0.0007264Direct


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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