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Mammalian Phenotype (MP): abnormal vascular regression

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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:   cardiovascular system phenotype [MP:0005385] <2>(67|85) (77|57|35)
+ + + + + 5:   mammalian phenotype [MP:0000001] <29>
+ + + + + 5:   abnormal cardiovascular system morphology [MP:0002127] <7>(48|65) (53|44|33)
+ + + + 4:   cellular phenotype [MP:0005384] <6>(95|116) (103|56|31)
+ + + + 4:   abnormal cardiovascular development [MP:0002925] <10>(16|35) (25|19|9)
+ + + + 4:   abnormal blood vessel morphology [MP:0001614] <29>(31|38) (36|27|24)
+ + + 3:   abnormal vascular development [MP:0000259] <9>(13|24) (18|13|5)
+ + + 3:   abnormal cell physiology [MP:0005621] <24>(77|96) (84|46|25)
+ + 2:   abnormal cell death [MP:0000313] <5>(29|41) (33|15|5)
+ + 2:   abnormal angiogenesis [MP:0000260] <8>(9|15) (12|9|4)
+ 1:   abnormal developmental vascular remodeling [MP:0009577] <1>(1|1) (1|1|0)
+ 1:   abnormal apoptosis [MP:0001648] <30>(27|38) (30|13|5)
0:   abnormal vascular regression [MP:0000364] <2>(1|1) (1|1|0)
- 1:   patent ductus arteriosus [MP:0003139](0|0) (0|0|0)
- 1:   patent ductus venosus [MP:0004004](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
PYP-like sensor domain (PAS domain)0.0008215Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Hypoxia-inducible factor Hif2a, C-terminal domain0.0002811Direct


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Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
PYP-like sensor domain (PAS domain)0.0004443Direct

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
47459,55785
  • 47459 - HLH, helix-loop-helix DNA-binding domain
  • 55785 - PYP-like sensor domain (PAS domain)
  • 0.0002212Direct


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