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Mammalian Phenotype (MP): abnormal gluconeogenesis

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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 glucose homeostasis [MP:0002078] <14>(15|22) (17|17|8)
0:   abnormal gluconeogenesis [MP:0003383](0|1) (0|1|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Hypoxia-inducible factor Hif2a, C-terminal domain0.0001094Direct


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Supra-domain (including individual superfamily)

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
47459,55785
  • 47459 - HLH, helix-loop-helix DNA-binding domain
  • 55785 - PYP-like sensor domain (PAS domain)
  • 0.0009218Direct