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Mammalian Phenotype (MP): abnormal manchette morphology

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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)
+ + + + + + + 7:   mammalian phenotype [MP:0000001] <29>
+ + + + + 5:   cellular phenotype [MP:0005384] <6>(95|116) (103|56|31)
+ + + + + 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)
+ + + + 4:   abnormal cell morphology [MP:0000358] <12>(19|19) (22|9|2)
+ + + 3:   abnormal gametogenesis [MP:0001929] <7>(15|19) (19|3|1)
+ + + 3:   abnormal germ cell morphology [MP:0002208] <5>(11|12) (13|2|1)
+ + 2:   abnormal male germ cell morphology [MP:0006362] <5>(7|8) (9|2|0)
+ + 2:   abnormal spermatogenesis [MP:0001156] <10>(8|13) (11|3|0)
+ 1:   abnormal spermatid morphology [MP:0006380] <1>(0|0) (0|0|0)
0:   abnormal manchette morphology [MP:0009376] <1>(0|0) (0|0|0)
- 1:   ectopic manchette [MP:0009377](0|0) (0|0|0)