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Mammalian Phenotype (MP): abnormal muscle cell glucose uptake

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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)
+ + + 3:   cellular phenotype [MP:0005384] <6>(95|116) (103|56|31)
+ + + 3:   mammalian phenotype [MP:0000001] <29>
+ + 2:   muscle phenotype [MP:0005369] <2>(49|57) (54|37|28)
+ + 2:   abnormal cell physiology [MP:0005621] <24>(77|96) (84|46|25)
+ 1:   abnormal cellular glucose import [MP:0003925] <3>(1|1) (1|1|0)
+ 1:   abnormal muscle physiology [MP:0002106] <23>(25|33) (27|16|11)
0:   abnormal muscle cell glucose uptake [MP:0004130] <1>(1|1) (1|0|0)
- 1:   abnormal cardiac cell glucose uptake [MP:0004039](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Lipocalins0.0008387Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Fatty acid binding protein-like0.0001087Direct


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)
Lipocalins0.0004541Direct


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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