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Mammalian Phenotype (MP): abnormal esophageal smooth muscle 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)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   digestive/alimentary phenotype [MP:0005381] <2>(38|46) (40|19|9)
+ + + 3:   muscle phenotype [MP:0005369] <2>(49|57) (54|37|28)
+ + 2:   abnormal digestive system morphology [MP:0000462] <21>(30|38) (31|13|3)
+ + 2:   abnormal muscle morphology [MP:0002108] <16>(28|31) (31|22|21)
+ 1:   abnormal esophagus morphology [MP:0000467] <14>(2|2) (2|1|0)
+ 1:   abnormal smooth muscle morphology [MP:0000767] <13>(6|6) (6|1|0)
0:   abnormal esophageal smooth muscle morphology [MP:0003159](1|1) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
"Winged helix" DNA-binding domain0.0009582Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Forkhead DNA-binding domain0.00007753Direct


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)
"Winged helix" DNA-binding domain0.0005219Direct


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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