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Mammalian Phenotype (MP): abnormal kidney epithelial cell primary cilium physiology

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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)
+ + + + + 5:   cellular phenotype [MP:0005384] <6>(95|116) (103|56|31)
+ + + + 4:   abnormal cell physiology [MP:0005621] <24>(77|96) (84|46|25)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   abnormal cilium physiology [MP:0013208] <2>(0|0) (0|0|0)
+ + + 3:   renal/urinary system phenotype [MP:0005367] <2>(41|47) (46|26|11)
+ + 2:   abnormal primary cilium physiology [MP:0013210] <2>(0|0) (0|0|0)
+ + 2:   abnormal renal/urinary system physiology [MP:0005502] <6>(20|21) (25|10|1)
+ 1:   abnormal nonmotile primary cilium physiology [MP:0013211] <2>(0|0) (0|0|0)
+ 1:   abnormal kidney physiology [MP:0002136] <22>(12|15) (14|5|1)
0:   abnormal kidney epithelial cell primary cilium physiology [MP:0011744](0|0) (0|0|0)