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Mammalian Phenotype (MP): abnormal melanoblast migration

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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:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ + + + + + 6:   abnormal embryo morphology [MP:0014134] <4>(23|31) (26|14|12)
+ + + + + + 6:   abnormal nervous system morphology [MP:0003632] <17>(76|104) (91|64|47)
+ + + + + 5:   abnormal nervous system development [MP:0003861] <9>(19|31) (21|14|10)
+ + + + + 5:   abnormal embryonic tissue morphology [MP:0002085] <35>(17|21) (19|10|9)
+ + + + + 5:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   abnormal neural tube morphology [MP:0002151] <16>(7|8) (7|4|3)
+ + + + 4:   cellular phenotype [MP:0005384] <6>(95|116) (103|56|31)
+ + + + 4:   embryo phenotype [MP:0005380] <7>(40|54) (46|28|19)
+ + + 3:   abnormal neural crest morphology [MP:0009846] <1>(0|0) (0|0|0)
+ + + 3:   abnormal embryonic tissue physiology [MP:0008932] <8>(1|3) (1|2|2)
+ + + 3:   abnormal cell physiology [MP:0005621] <24>(77|96) (84|46|25)
+ + 2:   abnormal neural crest cell physiology [MP:0012745] <4>(1|2) (1|2|2)
+ + 2:   abnormal neural crest cell morphology [MP:0009845] <8>(0|0) (0|0|0)
+ + 2:   abnormal cell migration [MP:0003091] <14>(13|16) (14|12|6)
+ 1:   abnormal melanoblast morphology [MP:0009783] <1>(0|0) (0|0|0)
+ 1:   abnormal neural crest cell migration [MP:0002950] <7>(1|1) (1|2|2)
0:   abnormal melanoblast migration [MP:0009784](0|0) (0|0|0)