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Mammalian Phenotype (MP): abnormal otic vesicle 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)
+ + + + 4:   mammalian phenotype [MP:0000001] <29>
+ + + 3:   hearing/vestibular/ear phenotype [MP:0005377] <2>(20|24) (23|14|5)
+ + 2:   abnormal ear morphology [MP:0002102] <4>(16|21) (18|14|5)
+ 1:   abnormal ear development [MP:0003938] <6>(1|0) (2|3|0)
0:   abnormal otic vesicle morphology [MP:0009806] <5>(0|0) (0|2|0)
- 1:   abnormal otic vesicle development [MP:0006030] <1>(0|0) (0|0|0)
- 1:   small otic vesicle [MP:0004310] <1>(0|0) (0|0|0)
- 1:   absent otic vesicle [MP:0004309](0|0) (0|0|0)
- 1:   decreased otic epithelial cell proliferation [MP:0008064](0|0) (0|0|0)
- 1:   increased otic epithelial cell apoptosis [MP:0008063](0|0) (0|0|0)


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Supra-domain (including individual superfamily)

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
50044,55550
  • 50044 - SH3-domain
  • 55550 - SH2 domain
  • 0.00009854Direct
    57716,57716
  • 57716 - Glucocorticoid receptor-like (DNA-binding domain)
  • 57716 - Glucocorticoid receptor-like (DNA-binding domain)
  • 0.0007794Direct