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Mammalian Phenotype (MP): abnormal red nucleus 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>
+ + + + + 5:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ + + + 4:   abnormal nervous system morphology [MP:0003632] <17>(76|104) (91|64|47)
+ + + 3:   abnormal brain morphology [MP:0002152] <24>(25|42) (35|24|14)
+ + + 3:   abnormal brainstem morphology [MP:0005277] <6>(2|5) (3|0|0)
+ + 2:   abnormal midbrain morphology [MP:0000897] <10>(2|4) (2|0|0)
+ 1:   abnormal tegmentum morphology [MP:0006100] <3>(1|1) (1|0|0)
0:   abnormal red nucleus morphology [MP:0012267] <1>(1|1) (1|0|0)
- 1:   absent red nucleus [MP:0012268](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Homeodomain-like0.00002418Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Homeodomain0.000004228Direct


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)
Homeodomain-like0.00001099Direct


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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