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Mammalian Phenotype (MP): failure of chorioallantoic fusion

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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)
+ + + + + + 6:   mammalian phenotype [MP:0000001] <29>
+ + + + + 5:   embryo phenotype [MP:0005380] <7>(40|54) (46|28|19)
+ + + + 4:   abnormal extraembryonic tissue physiology [MP:0004264] <10>(1|3) (2|2|1)
+ + + 3:   abnormal placenta physiology [MP:0010038] <5>(1|3) (2|1|0)
+ + 2:   abnormal placenta development [MP:0001712] <2>(1|3) (2|1|0)
+ 1:   abnormal chorioallantoic fusion [MP:0002824] <2>(1|3) (2|1|0)
0:   failure of chorioallantoic fusion [MP:0009657](0|1) (0|1|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Linker histone H1/H50.00001222Direct


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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)
50044,55550
  • 50044 - SH3-domain
  • 55550 - SH2 domain
  • 0.0008708Direct