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Mammalian Phenotype (MP): increased cochlear inner 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)
+ + + + + + + + + + + 11:   mammalian phenotype [MP:0000001] <29>
+ + + + + + + 7:   hearing/vestibular/ear phenotype [MP:0005377] <2>(20|24) (23|14|5)
+ + + + + + + 7:   abnormal membranous labyrinth morphology [MP:0000035] <2>(11|14) (12|9|5)
+ + + + + + 6:   abnormal cochlear labyrinth morphology [MP:0004426] <1>(10|12) (11|8|5)
+ + + + + + 6:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ + + + + + 6:   abnormal ear morphology [MP:0002102] <4>(16|21) (18|14|5)
+ + + + + 5:   abnormal scala media morphology [MP:0003169] <9>(10|12) (11|8|5)
+ + + + + 5:   abnormal inner ear morphology [MP:0000026] <15>(13|15) (13|11|5)
+ + + + + 5:   abnormal nervous system morphology [MP:0003632] <17>(76|104) (91|64|47)
+ + + + + 5:   abnormal mechanoreceptor morphology [MP:0000972] <4>(10|12) (10|7|5)
+ + + + + 5:   abnormal cochlea morphology [MP:0000031] <15>(12|14) (13|8|5)
+ + + + + 5:   abnormal somatic nervous system morphology [MP:0002752] <7>(34|47) (37|25|14)
+ + + + 4:   abnormal cochlear sensory epithelium morphology [MP:0003308] <1>(10|12) (10|7|5)
+ + + + 4:   abnormal somatic sensory system morphology [MP:0000959] <4>(26|38) (29|19|12)
+ + + + 4:   abnormal neuron morphology [MP:0002882] <29>(36|59) (40|26|19)
+ + + + 4:   abnormal neuron number [MP:0008946] <3>(8|16) (9|9|8)
+ + + + 4:   abnormal hair cell morphology [MP:0000045] <3>(10|12) (10|7|5)
+ + + + 4:   abnormal organ of Corti morphology [MP:0000042] <7>(10|12) (10|7|5)
+ + + 3:   abnormal cochlear hair cell morphology [MP:0002622] <6>(10|12) (10|7|5)
+ + + 3:   increased neuron number [MP:0008947] <8>(3|5) (4|4|4)
+ + + 3:   abnormal sensory neuron morphology [MP:0000965] <16>(16|28) (19|14|9)
+ + 2:   abnormal cochlear inner hair cell morphology [MP:0004393] <6>(5|5) (5|4|4)
+ + 2:   increased sensory neuron number [MP:0006006] <6>(3|5) (4|4|4)
+ + 2:   abnormal cochlear hair cell number [MP:0004406] <2>(1|3) (1|3|4)
+ 1:   abnormal cochlear inner hair cell number [MP:0004394] <2>(2|2) (2|3|4)
+ 1:   increased cochlear hair cell number [MP:0004407] <2>(1|3) (1|3|4)
0:   increased cochlear inner hair cell number [MP:0004395](1|1) (1|3|4)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
EGF/Laminin0.0002907Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
EGF-type module0.00002054Direct


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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/Laminin0.0001495Direct

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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
  • 0.000000008965Direct
    57184,57196
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 0.000003148Direct
    57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.000005861Direct

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    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57196,57184,57196
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 0.0000001206Direct
    57196,57196,57184
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.0000002519Direct
    57184,57196,57196
  • 57184 - Growth factor receptor domain
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.0000002519Direct
    57196,57196,57196
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 0.000007589Direct


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
    Plot tree as:   Download Newick format tree:
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