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Mammalian Phenotype (MP): abnormal cochlear hair cell stereociliary bundle 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)
+ + + + + + + + + 9:   mammalian phenotype [MP:0000001] <29>
+ + + + + + + 7:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ + + + + + 6:   abnormal nervous system morphology [MP:0003632] <17>(76|104) (91|64|47)
+ + + + + 5:   abnormal somatic nervous system morphology [MP:0002752] <7>(34|47) (37|25|14)
+ + + + + 5:   hearing/vestibular/ear phenotype [MP:0005377] <2>(20|24) (23|14|5)
+ + + + + 5:   abnormal membranous labyrinth morphology [MP:0000035] <2>(11|14) (12|9|5)
+ + + + 4:   abnormal cochlear labyrinth morphology [MP:0004426] <1>(10|12) (11|8|5)
+ + + + 4:   abnormal ear morphology [MP:0002102] <4>(16|21) (18|14|5)
+ + + + 4:   abnormal somatic sensory system morphology [MP:0000959] <4>(26|38) (29|19|12)
+ + + 3:   abnormal inner ear morphology [MP:0000026] <15>(13|15) (13|11|5)
+ + + 3:   abnormal scala media morphology [MP:0003169] <9>(10|12) (11|8|5)
+ + + 3:   abnormal mechanoreceptor morphology [MP:0000972] <4>(10|12) (10|7|5)
+ + + 3:   abnormal cochlea morphology [MP:0000031] <15>(12|14) (13|8|5)
+ + 2:   abnormal organ of Corti morphology [MP:0000042] <7>(10|12) (10|7|5)
+ + 2:   abnormal cochlear sensory epithelium morphology [MP:0003308] <1>(10|12) (10|7|5)
+ + 2:   abnormal hair cell morphology [MP:0000045] <3>(10|12) (10|7|5)
+ 1:   abnormal cochlear hair cell morphology [MP:0002622] <6>(10|12) (10|7|5)
0:   abnormal cochlear hair cell stereociliary bundle morphology [MP:0004521] <8>(5|7) (6|2|1)
- 1:   abnormal inner hair cell stereociliary bundle morphology [MP:0004532] <6>(1|1) (1|0|0)
- 1:   abnormal outer hair cell stereociliary bundle morphology [MP:0004527] <6>(1|2) (2|2|1)
- 1:   abnormal cochlear hair cell inter-stereocilial links morphology [MP:0004577] <4>(0|0) (0|0|0)
- 1:   abnormal orientation of cochlear hair cell stereociliary bundles [MP:0004522] <2>(2|4) (3|1|1)
- 1:   decreased cochlear hair cell stereocilia number [MP:0004523] <2>(0|1) (0|0|0)
- 1:   short cochlear hair cell stereocilia [MP:0004524] <2>(2|2) (2|0|0)
- 1:   absent cochlear hair cell stereocilia [MP:0004526](0|0) (0|0|0)
- 1:   thin cochlear hair cell stereocilia [MP:0004525](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Cadherin-like0.00007279Direct
PDZ domain-like0.0002622Direct
Second domain of FERM0.004684Inherited
SH3-domain0.08481Inherited
Frizzled cysteine-rich domain0.1058Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
DIX domain0.000002604Direct
PDZ domain0.000009922Direct
Cadherin0.00002201Direct
DEP domain0.00004086Direct
SH3-domain0.05606Inherited
Frizzled cysteine-rich domain0.0695Inherited
Motor proteins0.1198Inherited


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Cadherin-like0.0000348Direct
PDZ domain-like0.0001341Direct
Second domain of FERM0.002791Inherited
SH3-domain0.06297Inherited
Frizzled cysteine-rich domain0.08039Inherited
EGF/Laminin0.3652Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
49313,49313
  • 49313 - Cadherin-like
  • 49313 - Cadherin-like
  • 0.00002238Direct
    50156,50156
  • 50156 - PDZ domain-like
  • 50156 - PDZ domain-like
  • 0.0001195Direct

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    49313,49313,49313
  • 49313 - Cadherin-like
  • 49313 - Cadherin-like
  • 49313 - Cadherin-like
  • 0.00001619Direct


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