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Mammalian Phenotype (MP): abnormal brain copper level

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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)
+ + + + + 5:   homeostasis/metabolism phenotype [MP:0005376] <7>(140|174) (149|96|44)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   abnormal homeostasis [MP:0001764] <27>(103|129) (113|73|31)
+ + + 3:   abnormal mineral homeostasis [MP:0005636] <4>(5|6) (5|1|0)
+ + + 3:   abnormal ion homeostasis [MP:0001765] <15>(9|12) (11|4|0)
+ + + 3:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ + 2:   abnormal nervous system morphology [MP:0003632] <17>(76|104) (91|64|47)
+ + 2:   abnormal copper homeostasis [MP:0003951] <1>(1|1) (1|0|0)
+ + 2:   abnormal mineral level [MP:0000192] <4>(3|4) (3|1|0)
+ 1:   abnormal brain morphology [MP:0002152] <24>(25|42) (35|24|14)
+ 1:   abnormal copper level [MP:0003952] <5>(1|1) (1|0|0)
0:   abnormal brain copper level [MP:0011213] <3>(1|1) (1|0|0)
- 1:   abnormal brainstem copper level [MP:0011216] <2>(0|0) (0|0|0)
- 1:   decreased brain copper level [MP:0011215] <1>(0|0) (0|0|0)
- 1:   increased brain copper level [MP:0011214] <1>(0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
HMA, heavy metal-associated domain0.000000000005924Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
HMA, heavy metal-associated domain0.000000000004719Direct


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)
HMA, heavy metal-associated domain0.000000000002145Direct


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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