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Mammalian Phenotype (MP): abnormal vitamin homeostasis

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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:   mammalian phenotype [MP:0000001] <29>
+ + 2:   homeostasis/metabolism phenotype [MP:0005376] <7>(140|174) (149|96|44)
+ 1:   abnormal homeostasis [MP:0001764] <27>(103|129) (113|73|31)
0:   abnormal vitamin homeostasis [MP:0004019] <3>(3|3) (3|0|0)
- 1:   abnormal vitamin level [MP:0005400] <5>(3|3) (3|0|0)
- 1:   abnormal response to vitamins [MP:0003639](0|0) (0|0|0)
- 1:   abnormal vitamin absorption [MP:0001671](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Lipocalins0.00004636Direct
NAD(P)-binding Rossmann-fold domains0.003599Inherited
Cytochrome P4500.005629Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Fatty acid binding protein-like0.0001963Direct
Cytochrome P4500.004453Inherited
ABC transporter ATPase domain-like0.006793Inherited


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Lipocalins0.00002175Direct
NAD(P)-binding Rossmann-fold domains0.002111Inherited
Cytochrome P4500.003392Inherited


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
Plot tree as:   Download Newick format tree:
(show help)