ENSMUSG00000030761


Mus musculus

Features
Gene ID: ENSMUSG00000030761
  
Biological name :Myo7a
  
Synonyms : Myo7a / P97479 / Unconventional myosin-VIIa
  
Possible biological names infered from orthology : myosin VIIA / Q13402
  
Species: Mus musculus
  
Chr. number: 7
Strand: -1
Band: E1
Gene start: 98051060
Gene end: 98119524
  
Corresponding Affymetrix probe sets: 10565634 (MoGene1.0st)   1421385_a_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000102745
Ensembl peptide - ENSMUSP00000102744
Ensembl peptide - ENSMUSP00000114944
Ensembl peptide - ENSMUSP00000146165
Ensembl peptide - ENSMUSP00000146114
Ensembl peptide - ENSMUSP00000082046
Ensembl peptide - ENSMUSP00000102739
NCBI entrez gene - 17921     See in Manteia.
MGI - MGI:104510
RefSeq - XM_011241691
RefSeq - NM_001256081
RefSeq - NM_001256082
RefSeq - NM_001256083
RefSeq - NM_008663
RefSeq - XM_006507427
RefSeq - XM_006507428
RefSeq - XM_006507429
RefSeq - XM_011241688
RefSeq - XM_011241689
RefSeq - XM_011241690
RefSeq Peptide - NP_032689
RefSeq Peptide - NP_001243010
RefSeq Peptide - NP_001243011
RefSeq Peptide - NP_001243012
swissprot - D3YUT5
swissprot - A0A0R4J113
swissprot - Q5MJ56
swissprot - A0A0U1RPX7
swissprot - A0A0U1RPT3
swissprot - P97479
Ensembl - ENSMUSG00000030761
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 myo7aaENSDARG00000099871Danio rerio
 myo7abENSDARG00000044632Danio rerio
 MYO7AENSGALG00000031450Gallus gallus
 MYO7AENSG00000137474Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Myo7b / Q99MZ6 / Unconventional myosin-VIIb / Q6PIF6* / myosin VIIB*ENSMUSG0000002438851
Myo10 / F8VQB6 / Mus musculus myosin X (Myo10), transcript variant 3, mRNA. / Q9HD67* / myosin X*ENSMUSG0000002227226
Myo9a / Q8C170 / Unconventional myosin-IXa / B2RTY4* / myosin IXA*ENSMUSG0000003958522
Myo5a / Q99104 / Unconventional myosin-Va / Q9Y4I1* / myosin VA*ENSMUSG0000003459321
Myo5b / myosin VB / Q9ULV0*ENSMUSG0000002588520
Myo5c / myosin VC / Q9NQX4*ENSMUSG0000003359020
Myo9b / myosin IXB / Q13459*ENSMUSG0000000467720
Myo6 / myosin VI / Q9UM54*ENSMUSG0000003357715


Protein motifs (from Interpro)
Interpro ID Name
 IPR000048  IQ motif, EF-hand binding site
 IPR000299  FERM domain
 IPR000857  MyTH4 domain
 IPR001452  SH3 domain
 IPR001609  Myosin head, motor domain
 IPR011993  PH-like domain superfamily
 IPR014352  FERM/acyl-CoA-binding protein superfamily
 IPR019748  FERM central domain
 IPR019749  Band 4.1 domain
 IPR027417  P-loop containing nucleoside triphosphate hydrolase
 IPR029071  Ubiquitin-like domain superfamily
 IPR035963  FERM superfamily, second domain
 IPR036028  SH3-like domain superfamily
 IPR036106  Class VII myosin, motor domain


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001845 phagolysosome assembly IMP
 biological_processGO:0006886 intracellular protein transport IMP
 biological_processGO:0006909 phagocytosis IMP
 biological_processGO:0007018 microtubule-based movement IEA
 biological_processGO:0007040 lysosome organization ISS
 biological_processGO:0007600 sensory perception IMP
 biological_processGO:0007601 visual perception ISO
 biological_processGO:0007605 sensory perception of sound ISS
 biological_processGO:0030030 cell projection organization IMP
 biological_processGO:0030048 actin filament-based movement ISO
 biological_processGO:0042472 inner ear morphogenesis IMP
 biological_processGO:0042490 mechanoreceptor differentiation IMP
 biological_processGO:0042491 inner ear auditory receptor cell differentiation IMP
 biological_processGO:0048563 post-embryonic animal organ morphogenesis IMP
 biological_processGO:0048839 inner ear development IMP
 biological_processGO:0050953 sensory perception of light stimulus ISO
 biological_processGO:0050957 equilibrioception ISO
 biological_processGO:0051875 pigment granule localization IMP
 biological_processGO:0051904 pigment granule transport IMP
 biological_processGO:0060088 auditory receptor cell stereocilium organization IMP
 biological_processGO:0060113 inner ear receptor cell differentiation IMP
 biological_processGO:0060122 inner ear receptor cell stereocilium organization IMP
 cellular_componentGO:0001750 photoreceptor outer segment ISS
 cellular_componentGO:0001917 photoreceptor inner segment ISS
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005765 lysosomal membrane ISO
 cellular_componentGO:0005829 cytosol ISS
 cellular_componentGO:0005856 cytoskeleton IEA
 cellular_componentGO:0005902 microvillus ISO
 cellular_componentGO:0005938 cell cortex IEA
 cellular_componentGO:0016324 apical plasma membrane IDA
 cellular_componentGO:0016459 myosin complex IEA
 cellular_componentGO:0031477 myosin VII complex IEA
 cellular_componentGO:0032391 photoreceptor connecting cilium IDA
 cellular_componentGO:0032420 stereocilium IDA
 cellular_componentGO:0042470 melanosome IDA
 cellular_componentGO:0045202 synapse ISS
 cellular_componentGO:1990435 upper tip-link density IEA
 molecular_functionGO:0000146 microfilament motor activity ISO
 molecular_functionGO:0000166 nucleotide binding IEA
 molecular_functionGO:0003774 motor activity IEA
 molecular_functionGO:0003777 microtubule motor activity IEA
 molecular_functionGO:0003779 actin binding IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0005516 calmodulin binding ISO
 molecular_functionGO:0005524 ATP binding IEA
 molecular_functionGO:0008017 microtubule binding IEA
 molecular_functionGO:0019904 protein domain specific binding IPI
 molecular_functionGO:0030507 spectrin binding ISO
 molecular_functionGO:0030898 actin-dependent ATPase activity IEA
 molecular_functionGO:0042803 protein homodimerization activity IEA
 molecular_functionGO:0043531 ADP binding IEA
 molecular_functionGO:0047485 protein N-terminus binding IEA
 molecular_functionGO:0051015 actin filament binding ISO


Pathways (from Reactome)
Pathway description
The canonical retinoid cycle in rods (twilight vision)


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000034 abnormal vestibule morphology "malformed cavity between the semicircular canals and the cochlea of the inner ear" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:1776]
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Allelic Composition: Myo6mpc285H/Myo6mpc285H
Genetic Background: involves: BALB/c * C3H/HeH * C57BL/6J

 MP:0000042 abnormal organ of Corti "abnormalities associated with the highly specialized epithelium in the floor of the ductus cochlearis; also referred to a spiral organ (organum spirale), or acoustic papilla" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

 MP:0000045 abnormal hair cell morphology "malformation of the sensory epithelial cells of the inner ear" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator]
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Allelic Composition: NhsXcat/Nhs+
Genetic Background: involves: DBA/2 * T STOCK

Allelic Composition: Myo7a3336SB/Myo7a3336SB
Genetic Background: involves: BALB/cRl

Allelic Composition: Myo7a4494SB/Myo7a4494SB
Genetic Background: involves: BALB/cRl

Allelic Composition: Myo7a816SB/Myo7a816SB
Genetic Background: involves: BALB/cRl

 MP:0000436 abnormal head movements "anomalous motion of the portion of the body containing the brain and organs of sight, hearing, taste, and smell " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Gcgrtm1Mjch/Gcgrtm1Mjch
Genetic Background: involves: 129 * C57BL/6J * SJL

 MP:0001005 abnormal rod morphology "structural or developmental anomaly of the photoreceptors that contain rhodopsin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Dnah11b2b598Clo/Dnah11b2b598Clo
Genetic Background: C57BL/6J-Dnah11b2b598Clo

 MP:0001265 reduced body size "smaller than average body weight, height and/or length of an organism compared to controls" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:23170]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

 MP:0001289 persistence of hyaloid capillary system "failure of the degeneration of the transient vascular system of the eye during development" [J:49840]
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Allelic Composition: Myo7atm1a(EUCOMM)Wtsi/Myo7atm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Myo7atm1a(EUCOMM)Wtsi/Wtsi

 MP:0001363 increased anxiety-related response "when compared to controls, subjects exhibit more responses thought to be indicative of anxiety in behavioral tests" [cwg:Carroll-Ann W. Goldsmith, Mouse Genome Informatics curator, J:49752, J:53060]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

 MP:0001394 circling "repeated, compulsive movement in a circle; often associated with inner ear defects" [MGI:CLS, J:61295]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

Allelic Composition: Myo7ash1-7J/Myo7ash1-7J
Genetic Background: STOCK Myo7ash1-7J/J

Allelic Composition: Myo7ash1-11J/Myo7ash1-11J
Genetic Background: C57BL/6J-Myo7ash1-11J/J

Allelic Composition: Myo7ash1-9J/Myo7ash1-9J
Genetic Background: involves: C3.MRL-Faslpr/J

Allelic Composition: Myo7ash1/Myo7ash1
Genetic Background: SH1/LeJ

Allelic Composition: Myo7apolka/Myo7apolka
Genetic Background: involves: C57BL/6J

Allelic Composition: Myo7ash1-8J/Myo7ash1-8J
Genetic Background: B6.Cg-Myo7ash1-8J/J

Allelic Composition: Myo7ash1-7J/Myo7ash1-8J
Genetic Background: B6.Cg-Myo7ash1-7J Myo7ash1-8J

Allelic Composition: Myo7aewaso/Myo7aewaso
Genetic Background: involves: C57BL/6J

Allelic Composition: Myo7am1Btlr/Myo7am1Btlr
Genetic Background: C57BL/6J-Myo7am1Btlr

 MP:0001399 hyperactivity "general restlessness or excessive movement; more frequent movement from one place to another" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409, J:57125]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

Allelic Composition: Myo7aHdb/Myo7aHdb
Genetic Background: C3HeB/FeJ-Myo7aHdb/Ieg

Allelic Composition: Myo7aHdb/Myo7a+
Genetic Background: C3HeB/FeJ-Myo7aHdb/Ieg

Allelic Composition: Myo7am1Btlr/Myo7am1Btlr
Genetic Background: C57BL/6J-Myo7am1Btlr

 MP:0001406 abnormal gait "unusual or distinctive way of walking" [J:65038]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

Allelic Composition: Myo7ash1-13J/Myo7ash1-13J
Genetic Background: C.Cg-Myo7ash1-13J/GrsrJ

 MP:0001408 stereotypic behavior "repetitive, invariant, perseverative motor patterns that do not appear to be purposeful" [What s wrong with my mouse?:ISBN 0-471-31639-3]
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Allelic Composition: Myo7atm1a(EUCOMM)Wtsi/Myo7atm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Myo7atm1a(EUCOMM)Wtsi/Wtsi

 MP:0001410 head bobbing "compulsive up and down movement of the head" [J:17123]
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Allelic Composition: Myo7aHdb/Myo7aHdb
Genetic Background: C3HeB/FeJ-Myo7aHdb/Ieg

Allelic Composition: Myo7aHdb/Myo7a+
Genetic Background: C3HeB/FeJ-Myo7aHdb/Ieg

Allelic Composition: Myo7ash1-8J/Myo7ash1-8J
Genetic Background: B6.Cg-Myo7ash1-8J/J

Allelic Composition: Myo7ash1-13J/Myo7ash1-13J
Genetic Background: C.Cg-Myo7ash1-13J/GrsrJ

 MP:0001489 decreased startle reflex "greater threshold or less severe reflex response to variable stimuli, often auditory; usually measured by amplitude of whole body flinch" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, What s Wrong With My Mouse?:ISBN 0-471-31639-3]
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Allelic Composition: Myo7apolka/Myo7apolka
Genetic Background: involves: C57BL/6J

 MP:0001512 trunk curl "posture of the trunk in a curled position" [cml:Cathleen M. Lutz , Mouse Genome Informatics Curator]
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Allelic Composition: Adamts6b2b2029Clo/Adamts6b2b2029Clo
Genetic Background: C57BL/6J-Adamts6b2b2029Clo

Allelic Composition: Myo7atm1a(EUCOMM)Wtsi/Myo7atm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Myo7atm1a(EUCOMM)Wtsi/Wtsi

 MP:0001522 impaired swimming "reduced ability or inability to swim" [J:45446, J:39081]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Myo7ash1/Myo7ash1
Genetic Background: SH1/LeJ

Allelic Composition: Myo7apolka/Myo7apolka
Genetic Background: involves: C57BL/6J

 MP:0001523 impaired righting response "reduced ability or greater amount of time needed to recover from supine position" [J:25565]
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Allelic Composition: Myo7atm1a(EUCOMM)Wtsi/Myo7atm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Myo7atm1a(EUCOMM)Wtsi/Wtsi

 MP:0001525 impaired balance "reduced ability of an animal to maintain equilibrium" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:64962, J:17123]
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Allelic Composition: Leprdb-1R/Leprdb-1R
Genetic Background: involves: D7R75M

 MP:0001922 reduced male fertility "reduced ability of male to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61340]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

 MP:0001925 male infertility "inability of male to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

 MP:0001963 abnormal hearing "anomaly in the ability to receive auditory stimuli" [Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: NhsXcat/Nhs+
Genetic Background: involves: DBA/2 * T STOCK

Allelic Composition: Myo7a3336SB/Myo7a3336SB
Genetic Background: involves: BALB/cRl

Allelic Composition: Myo7a4494SB/Myo7a4494SB
Genetic Background: involves: BALB/cRl

Allelic Composition: Myo7a816SB/Myo7a816SB
Genetic Background: involves: BALB/cRl

 MP:0001967 deafness "inability to hear" [J:57651]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Myo7ash1-7J/Myo7ash1-7J
Genetic Background: STOCK Myo7ash1-7J/J

Allelic Composition: Myo7ash1-9J/Myo7ash1-9J
Genetic Background: involves: C3.MRL-Faslpr/J

Allelic Composition: Cdh23v/Cdh23+,Myo7ash1/Myo7a+
Genetic Background: involves: BALB

Allelic Composition: Myo7ampc142H/Myo7ampc142H
Genetic Background: involves: BALB/c * C3H/HeH * C57BL/6J

 MP:0002068 abnormal parental behavior "altered behavior of animals towards offspring" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Hrrh/Hrrh
Genetic Background: RHJ/LeJ

 MP:0002183 gliosis "increased growth pattern of neuroglia in a damaged area of the brain or spinal cord" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

 MP:0002622 abnormal cochlear hair cell morphology "malformation of the sensory epithelial cells of the cochlea; these cells are in synaptic contact with the auditory nerve" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

 MP:0002730 head shaking "compulsive movement of the head in the horizontal plane" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:274]
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Allelic Composition: Myo7ash1-7J/Myo7ash1-7J
Genetic Background: STOCK Myo7ash1-7J/J

Allelic Composition: Myo7ash1-13J/Myo7ash1-13J
Genetic Background: C.Cg-Myo7ash1-13J/GrsrJ

 MP:0002857 cochlear ganglion degeneration "loss of neural cell bodies in the group of nerve cell bodies that conveys auditory sensation from the organ of Corti to the hindbrain" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

 MP:0003382 straub tail "condition in which an animal carries its tail in an erect (vertical or nearly vertical) position; often seen upon opioid and other drug treatment" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Myo7ash1-13J/Myo7ash1-13J
Genetic Background: C.Cg-Myo7ash1-13J/GrsrJ

 MP:0003878 abnormal ear physiology "anomolous function of the ear, not due to an anatomical defect" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:100987]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

 MP:0003961 decreased lean body mass "less than average fat-free physical bulk or volume of the body including all its components except adipose tissue" [honda:Hiraoki Onda, Mouse GEnome Informatics Curator]
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Allelic Composition: Myo7atm1a(EUCOMM)Wtsi/Myo7atm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Myo7atm1a(EUCOMM)Wtsi/Wtsi

 MP:0004331 saccular macula degeneration "degeneration or loss of the oval neuroepithelial sensory receptor in the anterior wall of the saccule" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

 MP:0004362 cochlear hair cell degeneration "degeneration or loss of the sensory epithelial cells of the cochlea; these cells are in synaptic contact with the auditory nerve" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

Allelic Composition: Myo7aewaso/Myo7aewaso
Genetic Background: involves: C57BL/6J

 MP:0004363 stria vascularis degeneration "degeneration or loss of the stratified, secretory epithelium which lines the upper part of the cochlear spiral ligament and maintains potassium ion homeostasis in the endolymph" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

 MP:0004399 abnormal cochlear outer hair cell morphology "any structural abnormality in the sensory cells of the organ of Corti which are in synaptic contact with sensory as well as efferent fibers of the auditory nerve; there are three rows of columnar outer hair cells largely surrounded by cortilymph and supporting phalangeal cells; the apical end of each cell is anchored to the cuticular plate and about 100 stereocilia arranged in a V-shaped pattern extend from the cell s surface through the cuticular plate into the tectorial membrane" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Meox2tm1(cre)Sor/0,Pcsk5tm2Prat/Pcsk5tm2.1Prat
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * SJL

Allelic Composition: Myo7aewaso/Myo7aewaso
Genetic Background: involves: C57BL/6J

 MP:0004402 decreased cochlear outer hair cell number "decreased number (or less than the expected 3 rows) of the columnar outer hair sensory cells of the organ of Corti" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Cdh23v/Cdh23+
Genetic Background: involves: BALB/cRl * 47BS/Rl * CBA/Ca

Allelic Composition: Cdh23v/Cdh23+,Myo7a4626SB/Myo7a+
Genetic Background: involves: BALB/cRl * 47BS/Rl * CBA/Ca

 MP:0004404 cochlear outer hair cell degeneration "degeneration or loss of the columnar outer hair sensory cells of the organ of Corti" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Meox2tm1(cre)Sor/0,Pcsk5tm2Prat/Pcsk5tm2.1Prat
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * SJL

 MP:0004413 absent cochlear microphonics "absence or loss of the bioelectric potentials produced by the hair cells of the organ of Corti in response to sound" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7a816SB/Myo7a816SB
Genetic Background: involves: BALB/cRl

 MP:0004415 abnormal cochlear nerve compound action potential "anomaly in the combined potentials resulting from activation of the auditory division of the eighth cranial nerve; these potentials represent the summed activity of multiple cochlear afferent fibers discharging synchronously and thus assess the combined functional state of OHCs, IHCs, and their primary afferent innervation" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Cdh23v/Cdh23+
Genetic Background: involves: BALB/cRl * 47BS/Rl * CBA/Ca

Allelic Composition: Cdh23v/Cdh23+,Myo7a4626SB/Myo7a+
Genetic Background: involves: BALB/cRl * 47BS/Rl * CBA/Ca

 MP:0004466 short cochlear outer hair cells 
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Allelic Composition: Meox2tm1(cre)Sor/0,Pcsk5tm2Prat/Pcsk5tm2.1Prat
Genetic Background: involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * SJL

 MP:0004491 abnormal orientation of outer hair cell stereociliary bundles "misorientation or rotation of outer hair cell (OHC) stereociliary bundles, resulting in defective planar cell polarity of the inner ear sensory epithelium " [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Pex11atm1Itl/Pex11atm1Itl
Genetic Background: C57BL/6-Pex11atm1Itl

 MP:0004492 abnormal orientation of inner hair cell stereociliary bundles "misorientation or rotation of inner hair cell (IHC) stereociliary bundles, resulting in defective planar cell polarity of the inner ear sensory epithelium" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7aewaso/Myo7aewaso
Genetic Background: involves: C57BL/6J

 MP:0004515 abnormal vestibular hair cell stereociliary bundle morphology "any structural anomaly or disruption of the typical staircase-like arrangement of the mechanosensitive hair bundles which are composed of thick long microvilli (stereocilia) and are located at the apical end of vestibular hair cells of the utricle and saccule" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7aHdb/Myo7a+
Genetic Background: C3HeB/FeJ-Myo7aHdb/Ieg

Allelic Composition: Myo7ash1-8J/Myo7ash1-8J
Genetic Background: B6.Cg-Myo7ash1-8J/J

Allelic Composition: Myo7aewaso/Myo7aewaso
Genetic Background: involves: C57BL/6J

Allelic Composition: Myo7admbo2/Myo7admbo2
Genetic Background: involves: C57BL/6J

 MP:0004517 decreased vestibular hair cell stereocilia number "decreased number of the nonmotile, actin-filled specialized microvilli (stereocilia) normally arrayed on vestibular hair cells in a staircase-like pattern" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7aewaso/Myo7aewaso
Genetic Background: involves: C57BL/6J

 MP:0004521 abnormal cochlear hair cell stereociliary bundle morphology "any structural anomaly or disruption of the typical pattern of arrangement of mechanosensitive hair bundles which are composed of thick long microvilli (stereocilia) and are located at the apical end of cochlear inner and outer hair cells" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7a816SB/Myo7a816SB
Genetic Background: involves: BALB/cRl

Allelic Composition: Myo7apolka/Myo7apolka
Genetic Background: involves: C57BL/6J

Allelic Composition: Myo7a4626SB/Myo7a4626SB
Genetic Background: involves: 129S7/SvEvBrd * BALB/cRl * C3H * C57BL/6J * CBA/Ca

Allelic Composition: Myo7ash1-8J/Myo7ash1-8J
Genetic Background: B6.Cg-Myo7ash1-8J/J

Allelic Composition: Myo7admbo2/Myo7admbo2
Genetic Background: involves: C57BL/6J

 MP:0004522 abnormal orientation of cochlear hair cell stereociliary bundles "misorientation or rotation of inner and/or outer hair cell stereociliary bundles, resulting in defective planar cell polarity of the inner ear sensory epithelium" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7a816SB/Myo7a816SB
Genetic Background: involves: BALB/cRl

Allelic Composition: Myo7a4626SB/Myo7a4626SB
Genetic Background: involves: BALB/cRl

 MP:0004524 short cochlear hair cell stereocilia "reduced length of the nonmotile, actin-filled specialized microvilli (stereocilia) which are normally arrayed on cochlear inner and outer hair cells" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7apolka/Myo7apolka
Genetic Background: involves: C57BL/6J

 MP:0004527 abnormal outer hair cell stereociliary bundle morphology "any structural anomaly or disruption of the typical V or W-like pattern of arrangement of mechanosensitive hair bundles located at the apical end of cochlear OHCs; each hair bundle is normally composed of ~100 nonmotile, actin-filled microvilli (stereocilia) arranged in rows of increasing height and coupled to one another by morphologically distinct links: tip links, horizontal top connectors, shaft connectors, and ankle links; most hair bundles also possess a single motile kinocilium immediately adjacent to the tallest (outermost) row of stereocilia; a fifth link type, the kinocilial link, connects the kinocilium to its neighboring stereocilia" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7aHdb/Myo7aHdb
Genetic Background: C3HeB/FeJ-Myo7aHdb/Ieg

Allelic Composition: Myo7aHdb/Myo7a+
Genetic Background: C3HeB/FeJ-Myo7aHdb/Ieg

Allelic Composition: Myo7aHdb/Myo7a4626SB
Genetic Background: involves: BALB/c * 47BS/Rl * C3HeB/FeJ * CBA/Ca

Allelic Composition: Myo7a4626SB/Myo7a4626SB
Genetic Background: involves: BALB/cRl * 47BS/Rl * C3Hf/Rl * C57BL/10Rl * CBA/Ca

Allelic Composition: Cdh23v/Cdh23v,Myo7a4626SB/Myo7a+
Genetic Background: mixed

Allelic Composition: Cdh23v/Cdh23+,Myo7a4626SB/Myo7a4626SB
Genetic Background: mixed

Allelic Composition: Cdh23v/Cdh23v,Myo7a4626SB/Myo7a4626SB
Genetic Background: mixed

Allelic Composition: Myo7a4626SB/Myo7a+
Genetic Background: involves: BALB/cRl * 47BS/Rl * CBA/Ca

Allelic Composition: Cdh23v/Cdh23+,Myo7a4626SB/Myo7a+
Genetic Background: involves: BALB/cRl * 47BS/Rl * CBA/Ca

 MP:0004529 decreased outer hair cell stereocilia number "decreased number (or less than the expected 100 or so) of the nonmotile, actin-filled specialized microvilli (stereocilia) normally arrayed on cochlear outer hair cells" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7aHdb/Myo7aHdb
Genetic Background: C3HeB/FeJ-Myo7aHdb/Ieg

Allelic Composition: Myo7a4626SB/Myo7a+
Genetic Background: involves: BALB/cRl * 47BS/Rl * CBA/Ca

Allelic Composition: Cdh23v/Cdh23+,Myo7a4626SB/Myo7a+
Genetic Background: involves: BALB/cRl * 47BS/Rl * CBA/Ca

Allelic Composition: Myo7aewaso/Myo7aewaso
Genetic Background: involves: C57BL/6J

 MP:0004532 abnormal inner hair cell stereociliary bundle morphology "any structural anomaly or disruption of the typically linear or U-shaped pattern of arrangement of mechanosensitive hair bundles located at the apical end of cochlear IHCs; each hair bundle is normally composed of ~100 nonmotile, actin-filled microvilli (stereocilia) arranged in rows of increasing height and coupled to one another by morphologically distinct links: tip links, horizontal top connectors, shaft connectors, and ankle links; most hair bundles also possess a single motile kinocilium immediately adjacent to the tallest row of stereocilia; a fifth link type, the kinocilial link, connects the kinocilium to its neighboring stereocilia" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7aHdb/Myo7aHdb
Genetic Background: C3HeB/FeJ-Myo7aHdb/Ieg

Allelic Composition: Myo7aHdb/Myo7a+
Genetic Background: C3HeB/FeJ-Myo7aHdb/Ieg

Allelic Composition: Myo7aHdb/Myo7a4626SB
Genetic Background: involves: BALB/c * 47BS/Rl * C3HeB/FeJ * CBA/Ca

Allelic Composition: Myo7a4626SB/Myo7a4626SB
Genetic Background: involves: BALB/cRl

Allelic Composition: Myo7aewaso/Myo7aewaso
Genetic Background: involves: C57BL/6J

Allelic Composition: Myo7admbo2/Myo7admbo2
Genetic Background: involves: C57BL/6J

 MP:0004533 fused inner hair cell stereocilia "coalescence of the nonmotile, actin-filled specialized microvilli (stereocilia) normally arrayed on cochlear inner hair cells, often resulting in giant stereocilia" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7aHdb/Myo7aHdb
Genetic Background: C3HeB/FeJ-Myo7aHdb/Ieg

Allelic Composition: Myo7aHdb/Myo7a+
Genetic Background: C3HeB/FeJ-Myo7aHdb/Ieg

Allelic Composition: Myo7aHdb/Myo7a4626SB
Genetic Background: involves: BALB/c * 47BS/Rl * C3HeB/FeJ * CBA/Ca

Allelic Composition: Myo7aewaso/Myo7aewaso
Genetic Background: involves: C57BL/6J

 MP:0004534 decreased inner hair cell stereocilia number "decreased number (or less than the expected 100 or so) of the nonmotile, actin-filled specialized microvilli (stereocilia) normally arrayed on cochlear inner hair cells" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7aHdb/Myo7aHdb
Genetic Background: C3HeB/FeJ-Myo7aHdb/Ieg

Allelic Composition: Myo7aewaso/Myo7aewaso
Genetic Background: involves: C57BL/6J

Allelic Composition: Myo7admbo2/Myo7admbo2
Genetic Background: involves: C57BL/6J

 MP:0004577 abnormal cochlear hair cell inter-stereocilial links "any structural abnormality in the morphologically and biochemically distinct link types that extend between the stereocilia of cochlear hair bundles; link types can be distinguished by their relative sensitivities to treatment with calcium chelators and the protease subtilisin; in the mature mouse cochlea, tip links and horizontal top connectors are the only inter-stereocilial links associated with the hair bundle; ankle links and transient lateral links are both prominent features of developing auditory hair bundles" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7a4626SB/Myo7a4626SB
Genetic Background: involves: BALB/cRl

 MP:0004582 absent cochlear hair bundle ankle links "absence of the long, single-stranded filaments that form a dense web or mesh around the base of cochlear hair bundles just above the region in which the stereocilia begin to taper down" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7a4626SB/Myo7a4626SB
Genetic Background: involves: BALB/cRl

 MP:0004598 abnormal cochlear basement membrane "any structural abnormality in the continuous basement membrane found within the membranous labyrinth of the cochlea, known to extend from the limbus, down to the inner sulcus, across the basilar membrane, up to the external sulcus to the spiral prominence and radiating into the spiral ligament enseathing the root cell processes" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7aewaso/Myo7aewaso
Genetic Background: involves: C57BL/6J

 MP:0004632 abnormal cochlear OHC efferent innervation "any changes in the morphology or number of efferent terminals, occurring as clusters, in the cochlear OHC region; normally, medial olivocochlear neurons, which are primarily found in rostral and ventral periolivary regions, project mainly to the contralateral cochlea, and terminate directly on OHCs" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

 MP:0004737 absent distortion product otoacoustic emissions "failure to create mechanical distortions in the inner ear when two primary tones are presented, indicating failure of outer hair cells to amplify basilar membrane motion" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7apolka/Myo7apolka
Genetic Background: involves: C57BL/6J

 MP:0004748 increased susceptibility to age-related hearing loss "greater than normal loss of hearing associated with advancing age, manifest as reduced ability to perceive or discriminate sounds; the pattern and age of onset vary" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Cdh23v-2J/Cdh23+
Genetic Background: mixed

Allelic Composition: Cdh23v-2J/Cdh23+,Myo7a4626SB/Myo7a+
Genetic Background: mixed

Allelic Composition: Myo7a4626SB/Myo7a+
Genetic Background: involves: BALB/cRl * 47BS/Rl * CBA/Ca

 MP:0004767 increased cochlear nerve compound action potential "greater combined potentials resulting from activation of the auditory division of the eighth cranial nerve" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7aHdb/Myo7aHdb
Genetic Background: C3HeB/FeJ-Myo7aHdb/Ieg

Allelic Composition: Myo7aHdb/Myo7a+
Genetic Background: C3HeB/FeJ-Myo7aHdb/Ieg

 MP:0004813 absent linear vestibular evoked potential "absence of the biphasic response elicited by linear acceleration transients (usually jerk pulses to an animal s head)" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7ash1/Myo7ash1
Genetic Background: SH1/LeJ

 MP:0004924 abnormal behavior "anomalies in the actions, reactions, or performance of an organism in response to external or internal stimuli compared to controls" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

 MP:0005191 head tilt "condition in which the portion of the body containing the brain and organs of sight, hearing, taste, and smell lists to the side" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Myo7ash1-7J/Myo7ash1-7J
Genetic Background: STOCK Myo7ash1-7J/J

Allelic Composition: Myo7ash1-11J/Myo7ash1-11J
Genetic Background: C57BL/6J-Myo7ash1-11J/J

 MP:0005201 abnormal retinal pigment epithelium morphology "anomaly in the epithelial layer of the retina composed of cells containing pigment granules " [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Myo7apolka/Myo7apolka
Genetic Background: involves: C57BL/6J

 MP:0005307 head tossing "compulsive flailing of the head in multiple directions" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Myo7ash1-13J/Myo7ash1-13J
Genetic Background: C.Cg-Myo7ash1-13J/GrsrJ

Allelic Composition: Myo7am1Btlr/Myo7am1Btlr
Genetic Background: C57BL/6J-Myo7am1Btlr

 MP:0005424 jerky movement "continuous, abrupt, faltering motions of the whole body or a portion of the body" [llw2:Linda Washburn , Mouse Genome Informatics Curator]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

 MP:0005551 abnormal eye electrophysiology "abnormal function of the eye as determined through electrophysiological recordings from single cells or summary recordings from multiple cells (e.g. electroretinogram)" [NMF:Stephanie Pretel, Neuroscience Mutagenesis Facility Curator]
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Allelic Composition: Cdh23v/Cdh23v
Genetic Background: involves: CBA/Ca

 MP:0005565 increased blood urea nitrogen level "high circulating concentration of nitrogen, in the form of urea; commonly used to measure renal function" [RGD:Rat Genome Database submission, Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Myo7atm1a(EUCOMM)Wtsi/Myo7atm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Myo7atm1a(EUCOMM)Wtsi/Wtsi

 MP:0005633 increased circulating sodium level "greater than the normal concentration in the blood of this metallic element, the most plentiful extracellular ion in the body and the principal determinant of extracellular fluid volume" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, RGD:Rat Genome Database submission]
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Allelic Composition: Myo7atm1a(EUCOMM)Wtsi/Myo7atm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Myo7atm1a(EUCOMM)Wtsi/Wtsi

 MP:0006325 impaired hearing "reduced ability to percieve auditory stimuli" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7a4626SB/Myo7a+
Genetic Background: involves: BALB/cRl * 47BS/Rl * CBA/Ca

Allelic Composition: Myo7ash1-8J/Myo7a+
Genetic Background: B6.Cg-Myo7ash1-8J/J

Allelic Composition: Myo7aewaso/Myo7aewaso
Genetic Background: involves: C57BL/6J

Allelic Composition: Myo7admbo2/Myo7admbo2
Genetic Background: involves: C57BL/6J

 MP:0006358 absent pinna reflex "complete failure to respond to an auditory stimulus by a characteristic ear twitch" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator", MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

Allelic Composition: Cdh23v/Cdh23+,Myo7a4626SB/Myo7a+
Genetic Background: mixed

Allelic Composition: Cdh23v-2J/Cdh23+,Myo7a4626SB/Myo7a+
Genetic Background: mixed

Allelic Composition: Myo7atm1a(EUCOMM)Wtsi/Myo7atm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Myo7atm1a(EUCOMM)Wtsi/Wtsi

 MP:0006359 absent startle reflex "failure to respond to variable stimuli, often auditory; usually measured by amplitude of whole body flinch" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator", MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7ash1-7J/Myo7ash1-8J
Genetic Background: B6.Cg-Myo7ash1-7J Myo7ash1-8J

 MP:0006388 abnormal auditory summating potiential "any anomaly in the dc shift in the waveform sustained for the duration of a toneburst stimulus that represents the depolarization of sensory hair cells in the cochlea; positive summating potentials (SPs) reflect activity of basal turn hair cells while negative SPs are derived from hair cell activity in the apical turn; negative SPs tend to be obtained at low frequencies and low intensities of stimulus, while positive SPs are recorded in response to high frequencies and high intensities " [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", PMID:1526886]
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Allelic Composition: Myo7a816SB/Myo7a816SB
Genetic Background: involves: BALB/cRl

 MP:0006409 vestibular ganglion hypoplasia "underdevelopment or reduced size, usually due to a reduced number of cell bodies, in the group of bipolar sensory nerve cell bodies concerned with equilibration that form a swelling on the vestibular part of the eighth cranial nerve in the fundus of the internal acoustic meatus" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

 MP:0008039 increased NK T cell number "greater number of the distinct lineage of T cells expressing natural killer cell markers and having T cell receptors characterized by the usage of a restricted repertoire of variable region gene segments" [GO:0001865]
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Allelic Composition: Myo7atm1a(EUCOMM)Wtsi/Myo7atm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Myo7atm1a(EUCOMM)Wtsi/Wtsi

 MP:0008451 retinal rod cell degeneration "a retrogressive impairment of function or destruction of one of the photoreceptor cell types of the vertebrate retina, in which the photopigment is in stacks of membranous disks separate from the outer cell membrane" [MESH:A08.663.650.650.670.650]
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Allelic Composition: Dnah11b2b598Clo/Dnah11b2b598Clo
Genetic Background: C57BL/6J-Dnah11b2b598Clo

 MP:0008489 postnatal slow weight gain "the weight gain over a span of postnatal developmental time is slower than controls, with or without ever attaining a similar weight to controls as adults" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

 MP:0010323 retropulsion "a tendency to step or walk backwards" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Myo7ash1-6J/Myo7ash1-6J
Genetic Background: involves: C57BLKS/J

Allelic Composition: Myo7ash1-13J/Myo7ash1-13J
Genetic Background: C.Cg-Myo7ash1-13J/GrsrJ

 MP:0011939 increased food intake "increase in the total number of calories/food amount taken in over time when compared to the normal state" [MGI:csmith]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

 MP:0011941 increased fluid intake "increase in the total amount of fluid taken in over time when compared to the normal state" [MGI:csmith]
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Allelic Composition: Aprttm1Dwm/Aprttm1Dwm
Genetic Background: 129P2/OlaHsd-Aprttm1Dwm

 MP:0011967 increased or absent threshold for auditory brainstem response "increase in the value at which one or more sound frequencies or broadband clicks first elicits a recordable response generated by electrical activity of neurons in the ascending auditory system, or complete lack of a recordable response at any frequency or broadband click" [MGI:csmith]
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Allelic Composition: Myo7apolka/Myo7apolka
Genetic Background: involves: C57BL/6J

Allelic Composition: Myo7ash1-8J/Myo7ash1-8J
Genetic Background: B6.Cg-Myo7ash1-8J/J

Allelic Composition: Myo7ash1-8J/Myo7a+,Ush1gjs/Ush1g+
Genetic Background: B6.Cg-Myo7ash1-8J Ush1gjs

Allelic Composition: Cdh23v-2J/Cdh23+,Myo7ash1-8J/Myo7a+
Genetic Background: B6.Cg-Myo7ash1-8J Cdh23v-2J

Allelic Composition: Myo7ash1-8J/Myo7a+,Pcdh15av-3J/Pcdh15+
Genetic Background: B6.Cg-Myo7ash1-8J Pcdh15av-3J

Allelic Composition: Myo7aewaso/Myo7aewaso
Genetic Background: involves: C57BL/6J

Allelic Composition: Myo7aewaso/Myo7a+
Genetic Background: involves: C57BL/6J

Allelic Composition: Myo7admbo2/Myo7admbo2
Genetic Background: involves: C57BL/6J

Allelic Composition: Myo7atm1a(EUCOMM)Wtsi/Myo7atm1a(EUCOMM)Wtsi
Genetic Background: C57BL/6N-Myo7atm1a(EUCOMM)Wtsi/Wtsi

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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