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Mammalian Phenotype (MP): arrest of male meiosis

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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)
+ + + + + + 6:   mammalian phenotype [MP:0000001] <29>
+ + + + + 5:   reproductive system phenotype [MP:0005389] <2>(38|58) (47|18|6)
+ + + + 4:   abnormal reproductive system morphology [MP:0002160] <12>(28|46) (37|15|6)
+ + + 3:   abnormal gametogenesis [MP:0001929] <7>(15|19) (19|3|1)
+ + 2:   abnormal meiosis [MP:0001930] <11>(4|5) (5|1|0)
+ + 2:   abnormal spermatogenesis [MP:0001156] <10>(8|13) (11|3|0)
+ 1:   arrest of spermatogenesis [MP:0001155] <2>(1|3) (1|0|0)
+ 1:   abnormal male meiosis [MP:0005169] <3>(3|4) (3|1|0)
0:   arrest of male meiosis [MP:0008261](0|1) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Histone lysine methyltransferases0.0008177Direct


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