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Mammalian Phenotype (MP): abnormal cochlear hair cell number

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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:   hearing/vestibular/ear phenotype [MP:0005377] <2>(20|24) (23|14|5)
+ + + + + 5:   abnormal somatic nervous system morphology [MP:0002752] <7>(34|47) (37|25|14)
+ + + + + 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 mechanoreceptor morphology [MP:0000972] <4>(10|12) (10|7|5)
+ + + 3:   abnormal scala media morphology [MP:0003169] <9>(10|12) (11|8|5)
+ + + 3:   abnormal cochlea morphology [MP:0000031] <15>(12|14) (13|8|5)
+ + + 3:   abnormal inner ear morphology [MP:0000026] <15>(13|15) (13|11|5)
+ + 2:   abnormal hair cell morphology [MP:0000045] <3>(10|12) (10|7|5)
+ + 2:   abnormal cochlear sensory epithelium morphology [MP:0003308] <1>(10|12) (10|7|5)
+ + 2:   abnormal organ of Corti morphology [MP:0000042] <7>(10|12) (10|7|5)
+ 1:   abnormal cochlear hair cell morphology [MP:0002622] <6>(10|12) (10|7|5)
0:   abnormal cochlear hair cell number [MP:0004406] <2>(1|3) (1|3|4)
- 1:   decreased cochlear hair cell number [MP:0004408] <3>(0|0) (0|0|0)
- 1:   increased cochlear hair cell number [MP:0004407] <2>(1|3) (1|3|4)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
EGF/Laminin0.05336Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
DIX domain0.000001165Direct
DEP domain0.00001909Direct
EGF-type module0.03074Inherited


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)
EGF/Laminin0.03788Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57196,57184
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.000003237Direct
    57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.000009739Direct
    57184,57196
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 0.0002579Direct

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57196,57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.000001156Direct
    57196,57184,57196
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 0.0000127Direct
    57184,57196,57196
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.00002539Direct
    57196,57196,57184
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.00002539Direct


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