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Mammalian Phenotype (MP): abnormal parietal bone morphology

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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)
+ + + + + + + 7:   mammalian phenotype [MP:0000001] <29>
+ + + + + + 6:   skeleton phenotype [MP:0005390] <2>(46|63) (50|41|26)
+ + + + + 5:   abnormal skeleton morphology [MP:0005508] <15>(41|59) (47|38|25)
+ + + + + 5:   craniofacial phenotype [MP:0005382] <1>(20|36) (24|17|10)
+ + + + 4:   abnormal axial skeleton morphology [MP:0002114] <4>(24|40) (25|21|14)
+ + + + 4:   abnormal craniofacial morphology [MP:0000428] <5>(20|36) (24|17|10)
+ + + 3:   abnormal craniofacial bone morphology [MP:0002116] <3>(16|25) (16|13|7)
+ + 2:   abnormal cranium morphology [MP:0000438] <11>(16|25) (16|13|7)
+ 1:   abnormal neurocranium morphology [MP:0000074] <11>(5|5) (5|3|0)
0:   abnormal parietal bone morphology [MP:0000109] <3>(0|0) (0|1|0)
- 1:   small parietal bone [MP:0004418] <1>(0|0) (0|0|0)
- 1:   absent parietal bone [MP:0004419](0|0) (0|0|0)
- 1:   enlarged parietal bone [MP:0004421](0|0) (0|0|0)


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Supra-domain (including individual superfamily)

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57184,57196
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 0.0002412Direct