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Mammalian Phenotype (MP): abnormal rostral-caudal axis patterning

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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:   embryo phenotype [MP:0005380] <7>(40|54) (46|28|19)
+ + 2:   abnormal embryo development [MP:0001672] <5>(9|15) (11|11|5)
+ 1:   abnormal developmental patterning [MP:0002084] <7>(7|12) (9|9|3)
0:   abnormal rostral-caudal axis patterning [MP:0005221] <5>(1|5) (1|1|0)
- 1:   abnormal rostral-caudal patterning of the somites [MP:0008530](0|0) (0|0|0)
- 1:   caudal body truncation [MP:0004073](0|0) (0|0|0)
- 1:   rostral body truncation [MP:0012157](0|0) (0|0|0)
- 1:   rostral-caudal axis duplication [MP:0012156](0|1) (0|0|0)
- 1:   short rostral-caudal axis [MP:0012173](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
SMAD MH1 domain0.00000002767Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
SMAD domain0.00000001861Direct
SMAD MH1 domain0.00000001861Direct
DIX domain0.00002191Direct
Linker histone H1/H50.0001355Direct
Extracellular domain of cell surface receptors0.0002083Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
SMAD MH1 domain0.00000001056Direct

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
63501,50242
  • 63501 - Frizzled cysteine-rich domain
  • 50242 - TIMP-like
  • 0.000005749Direct


    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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