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Mammalian Phenotype (MP): abnormal copper 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)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   homeostasis/metabolism phenotype [MP:0005376] <7>(140|174) (149|96|44)
+ + 2:   abnormal homeostasis [MP:0001764] <27>(103|129) (113|73|31)
+ 1:   abnormal mineral homeostasis [MP:0005636] <4>(5|6) (5|1|0)
+ 1:   abnormal ion homeostasis [MP:0001765] <15>(9|12) (11|4|0)
0:   abnormal copper homeostasis [MP:0003951] <1>(1|1) (1|0|0)
- 1:   abnormal copper level [MP:0003952] <5>(1|1) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
HMA, heavy metal-associated domain0Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
HMA, heavy metal-associated domain0Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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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)
HMA, heavy metal-associated domain0Direct


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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