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Mammalian Phenotype (MP): abnormal kidney epithelial cell primary cilium 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)
+ + + + + 5:   mammalian phenotype [MP:0000001] <29>
+ + + + + 5:   cellular phenotype [MP:0005384] <6>(95|116) (103|56|31)
+ + + + 4:   abnormal cell morphology [MP:0000358] <12>(19|19) (22|9|2)
+ + + + 4:   renal/urinary system phenotype [MP:0005367] <2>(41|47) (46|26|11)
+ + + 3:   abnormal cilium morphology [MP:0013202] <2>(3|2) (3|3|1)
+ + + 3:   abnormal renal/urinary system morphology [MP:0000516] <14>(31|36) (36|22|11)
+ + 2:   abnormal kidney morphology [MP:0002135] <29>(26|28) (28|15|6)
+ + 2:   abnormal primary cilium morphology [MP:0013203] <2>(3|2) (3|3|1)
+ 1:   abnormal kidney epithelium morphology [MP:0004967] <3>(4|3) (4|2|0)
+ 1:   abnormal nonmotile primary cilium morphology [MP:0013205] <7>(2|2) (2|2|1)
0:   abnormal kidney epithelial cell primary cilium morphology [MP:0011065] <4>(1|1) (1|1|0)
- 1:   abnormal renal tubule epithelial cell primary cilium morphology [MP:0011066](0|1) (0|0|0)
- 1:   absent kidney epithelial cell primary cilium [MP:0020384](0|0) (0|0|0)
- 1:   decreased kidney epithelial cell primary cilium length [MP:0020383](0|0) (0|0|0)
- 1:   increased kidney epithelial cell primary cilium length [MP:0020382](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
HCP-like0.000000107Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Tetratricopeptide repeat (TPR)0.01777Inherited


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Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
HCP-like0.00000004235Direct

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
48452,81901
  • 48452 - TPR-like
  • 81901 - HCP-like
  • 0.000000001299Direct


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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