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Mammalian Phenotype (MP): abnormal circulating carnitine 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:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   homeostasis/metabolism phenotype [MP:0005376] <7>(140|174) (149|96|44)
+ + + 3:   abnormal homeostasis [MP:0001764] <27>(103|129) (113|73|31)
+ + 2:   abnormal amino acid level [MP:0005332] <5>(8|9) (9|2|0)
+ + 2:   abnormal blood homeostasis [MP:0009642] <23>(63|82) (70|45|21)
+ 1:   abnormal circulating amino acid level [MP:0005311] <6>(7|8) (8|2|0)
0:   abnormal circulating carnitine level [MP:0003977] <2>(2|2) (2|1|0)
- 1:   decreased circulating carnitine level [MP:0003978](0|0) (0|0|0)
- 1:   increased circulating carnitine level [MP:0003979](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Acyl-CoA dehydrogenase NM domain-like0.00000000000003477Direct
Acyl-CoA dehydrogenase C-terminal domain-like0.00000000000003477Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Medium chain acyl-CoA dehydrogenase, NM (N-terminal and middle) domains0Direct
Medium chain acyl-CoA dehydrogenase-like, C-terminal domain0Direct


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)
Acyl-CoA dehydrogenase NM domain-like0.00000000000001253Direct
Acyl-CoA dehydrogenase C-terminal domain-like0.00000000000001253Direct

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
56645,47203
  • 56645 - Acyl-CoA dehydrogenase NM domain-like
  • 47203 - Acyl-CoA dehydrogenase C-terminal domain-like
  • 0.00000000000001253Direct


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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