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Mammalian Phenotype (MP): abnormal fibroblast migration

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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)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   cellular phenotype [MP:0005384] <6>(96|116) (103|56|31)
+ + 2:   abnormal cell physiology [MP:0005621] <24>(78|96) (84|46|25)
+ 1:   abnormal cell migration [MP:0003091] <14>(13|16) (14|12|6)
0:   abnormal fibroblast migration [MP:0011706] <2>(1|0) (1|0|0)
- 1:   decreased fibroblast cell migration [MP:0011708] <1>(1|0) (1|0|0)
- 1:   increased fibroblast cell migration [MP:0011709](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
BAR/IMD domain-like0.001328Inherited


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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)
BAR/IMD domain-like0.0007379Direct


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