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Mammalian Phenotype (MP): abnormal DNA methylation during gametogenesis

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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

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>
+ + + + 4:   cellular phenotype [MP:0005384] <6>(95|116) (103|56|31)
+ + + 3:   abnormal cell physiology [MP:0005621] <24>(77|96) (84|46|25)
+ + + 3:   reproductive system phenotype [MP:0005389] <2>(38|58) (47|18|6)
+ + 2:   abnormal epigenetic regulation of gene expression [MP:0012167] <5>(1|2) (2|0|0)
+ + 2:   abnormal reproductive system morphology [MP:0002160] <12>(28|46) (37|15|6)
+ 1:   abnormal DNA methylation [MP:0008877] <1>(1|1) (1|0|0)
+ 1:   abnormal gametogenesis [MP:0001929] <7>(15|19) (19|3|1)
0:   abnormal DNA methylation during gametogenesis [MP:0008878](1|0) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Tudor/PWWP/MBT0.0005453Direct


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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)
Tudor/PWWP/MBT0.0002894Direct


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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