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Search results 1501 to 1600 out of 1619 for Myo7a

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Type Details Score
Publication
37369584 | J:344891
First Author: Maunsell HR
Year: 2023
Journal: J Neurosci
Title: Lrrn1 Regulates Medial Boundary Formation in the Developing Mouse Organ of Corti.
Volume: 43
Issue: 29
Pages: 5305-5318
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Publication
20016102 | J:157099
First Author: Grimsley-Myers CM
Year: 2009
Journal: J Neurosci
Title: The small GTPase Rac1 regulates auditory hair cell morphogenesis.
Volume: 29
Issue: 50
Pages: 15859-69
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Publication
34001891 | J:306060
First Author: Kindt KS
Year: 2021
Journal: Nat Commun
Title: EMX2-GPR156-Gαi reverses hair cell orientation in mechanosensory epithelia.
Volume: 12
Issue: 1
Pages: 2861
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Publication
21831920 | J:180898
First Author: Brown AS
Year: 2011
Journal: Development
Title: Otic ablation of smoothened reveals direct and indirect requirements for Hedgehog signaling in inner ear development.
Volume: 138
Issue: 18
Pages: 3967-76
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Publication
20346939 | J:160473
First Author: Trowe MO
Year: 2010
Journal: Dev Biol
Title: Loss of Sox9 in the periotic mesenchyme affects mesenchymal expansion and differentiation, and epithelial morphogenesis during cochlea development in the mouse.
Volume: 342
Issue: 1
Pages: 51-62
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Publication
21420948 | J:173796
First Author: Yamamoto N
Year: 2011
Journal: Dev Biol
Title: Rbpj regulates development of prosensory cells in the mammalian inner ear.
Volume: 353
Issue: 2
Pages: 367-79
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Publication
24465223 | J:226669
First Author: Ono K
Year: 2014
Journal: PLoS Genet
Title: FGFR1-Frs2/3 signalling maintains sensory progenitors during inner ear hair cell formation.
Volume: 10
Issue: 1
Pages: e1004118
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Publication
22182523 | J:180774
First Author: Grimsley-Myers CM
Year: 2012
Journal: Dev Biol
Title: Redundant functions of Rac GTPases in inner ear morphogenesis.
Volume: 362
Issue: 2
Pages: 172-86
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Publication
23614009 | J:200106
First Author: Duncan JS
Year: 2013
Journal: PLoS One
Title: Continued expression of GATA3 is necessary for cochlear neurosensory development.
Volume: 8
Issue: 4
Pages: e62046
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Publication
30344048 | J:268688
First Author: Kim YJ
Year: 2018
Journal: Neuron
Title: Chd2 Is Necessary for Neural Circuit Development and Long-Term Memory.
Volume: 100
Issue: 5
Pages: 1180-1193.e6
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Publication
23666531 | J:199588
First Author: Luo XJ
Year: 2013
Journal: Hum Mol Genet
Title: GATA3 controls the specification of prosensory domain and neuronal survival in the mouse cochlea.
Volume: 22
Issue: 18
Pages: 3609-23
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Publication
31843520 | J:286655
First Author: Sakamoto S
Year: 2020
Journal: Dev Biol
Title: Idgenes are required for morphogenesis and cellular patterning in the developing mammalian cochlea.
Volume: 460
Issue: 2
Pages: 164-175
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Publication
23533177 | J:195272
First Author: Sipe CW
Year: 2013
Journal: Development
Title: Lis1 mediates planar polarity of auditory hair cells through regulation of microtubule organization.
Volume: 140
Issue: 8
Pages: 1785-95
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Publication
- | J:82238
     
First Author: JAX Neuroscience Mutagenesis Facility
Year: 2003
Journal: MGI Direct Data Submission
Title: Heritable mouse mutants from JAX NMF ENU Mutagenesis Program
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Publication
23193000 | J:191198
First Author: Kopecky BJ
Year: 2013
Journal: Dev Dyn
Title: Correct timing of proliferation and differentiation is necessary for normal inner ear development and auditory hair cell viability.
Volume: 242
Issue: 2
Pages: 132-47
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Publication
30814219 | J:273200
First Author: Landin Malt A
Year: 2019
Journal: Proc Natl Acad Sci U S A
Title: Par3 is essential for the establishment of planar cell polarity of inner ear hair cells.
Volume: 116
Issue: 11
Pages: 4999-5008
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Publication
35790771 | J:326535
First Author: Petitpré C
Year: 2022
Journal: Nat Commun
Title: Single-cell RNA-sequencing analysis of the developing mouse inner ear identifies molecular logic of auditory neuron diversification.
Volume: 13
Issue: 1
Pages: 3878
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Publication
23946445 | J:204446
First Author: Tateya T
Year: 2013
Journal: Development
Title: Hedgehog signaling regulates prosensory cell properties during the basal-to-apical wave of hair cell differentiation in the mammalian cochlea.
Volume: 140
Issue: 18
Pages: 3848-57
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Publication
35508658 | J:330325
First Author: García-Añoveros J
Year: 2022
Journal: Nature
Title: Tbx2 is a master regulator of inner versus outer hair cell differentiation.
Volume: 605
Issue: 7909
Pages: 298-303
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Publication
35320729 | J:324832
First Author: Sun Y
Year: 2022
Journal: Cell Rep
Title: Single-cell transcriptomic landscapes of the otic neuronal lineage at multiple early embryonic ages.
Volume: 38
Issue: 12
Pages: 110542
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Publication
36074819 | J:333967
First Author: Filova I
Year: 2022
Journal: Proc Natl Acad Sci U S A
Title: ISL1 is necessary for auditory neuron development and contributes toward tonotopic organization.
Volume: 119
Issue: 37
Pages: e2207433119
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Publication
39373109 | J:359963
 
First Author: de Haan S
Year: 2024
Journal: Development
Title: Jag1 represses Notch activation in lateral supporting cells and inhibits an outer hair cell fate in the medial cochlea.
Volume: 151
Issue: 21
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Publication
24721909 | J:209956
 
First Author: Liakath-Ali K
Year: 2014
Journal: Nat Commun
Title: Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen.
Volume: 5
Pages: 3540
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Publication
32907846 | J:297063
 
First Author: Najarro EH
Year: 2020
Journal: Development
Title: Dual regulation of planar polarization by secreted Wnts and Vangl2 in the developing mouse cochlea.
Volume: 147
Issue: 19
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Publication
24727668 | J:214677
First Author: Bohnenpoll T
Year: 2014
Journal: Dev Biol
Title: Canonical Wnt signaling regulates the proliferative expansion and differentiation of fibrocytes in the murine inner ear.
Volume: 391
Issue: 1
Pages: 54-65
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Publication
20111592 | J:223633
First Author: Sanchez-Calderon H
Year: 2010
Journal: PLoS One
Title: RNA microarray analysis in prenatal mouse cochlea reveals novel IGF-I target genes: implication of MEF2 and FOXM1 transcription factors.
Volume: 5
Issue: 1
Pages: e8699
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Publication
25624266 | J:221167
First Author: Urness LD
Year: 2015
Journal: Dev Biol
Title: Fgf10 is required for specification of non-sensory regions of the cochlear epithelium.
Volume: 400
Issue: 1
Pages: 59-71
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Publication
27534441 | J:234901
 
First Author: Potter PK
Year: 2016
Journal: Nat Commun
Title: Novel gene function revealed by mouse mutagenesis screens for models of age-related disease.
Volume: 7
Pages: 12444
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Publication
29107558 | J:245876
First Author: Rohacek AM
Year: 2017
Journal: Dev Cell
Title: ESRP1 Mutations Cause Hearing Loss due to Defects in Alternative Splicing that Disrupt Cochlear Development.
Volume: 43
Issue: 3
Pages: 318-331.e5
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Publication
8884266 | J:35477
First Author: Hasson T
Year: 1996
Journal: Genomics
Title: Mapping of unconventional myosins in mouse and human.
Volume: 36
Issue: 3
Pages: 431-9
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Publication
37279265 | J:343328
First Author: Xie Z
Year: 2023
Journal: Proc Natl Acad Sci U S A
Title: ZBTB20 is essential for cochlear maturation and hearing in mice.
Volume: 120
Issue: 24
Pages: e2220867120
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Publication
30938680 | J:274697
   
First Author: Celaya AM
Year: 2019
Journal: Elife
Title: Deficit of mitogen-activated protein kinase phosphatase 1 (DUSP1) accelerates progressive hearing loss.
Volume: 8
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Publication
34003106 | J:307862
   
First Author: Wilkerson BA
Year: 2021
Journal: Elife
Title: Novel cell types and developmental lineages revealed by single-cell RNA-seq analysis of the mouse crista ampullaris.
Volume: 10
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Publication
25917818 | J:222308
First Author: Fairfield H
Year: 2015
Journal: Genome Res
Title: Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders.
Volume: 25
Issue: 7
Pages: 948-57
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Publication
23055939 | J:193641
First Author: Nakano Y
Year: 2012
Journal: PLoS Genet
Title: A mutation in the Srrm4 gene causes alternative splicing defects and deafness in the Bronx waltzer mouse.
Volume: 8
Issue: 10
Pages: e1002966
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Publication
30995482 | J:281311
First Author: Nakano Y
Year: 2019
Journal: Cell Rep
Title: Overlapping Activities of Two Neuronal Splicing Factors Switch the GABA Effect from Excitatory to Inhibitory by Regulating REST.
Volume: 27
Issue: 3
Pages: 860-871.e8
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Publication
- | J:175295
     
First Author: Mouse Genome Informatics and the Wellcome Trust Sanger Institute Mouse Genetics Project (MGP)
Year: 2011
Journal: Database Release
Title: Obtaining and Loading Phenotype Annotations from the Wellcome Trust Sanger Institute (WTSI) Mouse Resources Portal
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Publication
38355793 | J:345621
First Author: Adams DJ
Year: 2024
Journal: Nature
Title: Genetic determinants of micronucleus formation in vivo.
Volume: 627
Issue: 8002
Pages: 130-136
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Publication
- | J:15839
       
First Author: International Committee on Standardized Genetic Nomenclature for Mice
Year: 1993
Title: Nomenclature rule change to delete hyphens and parentheses from mouse locus symbols
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Publication
30973865 | J:274872
First Author: Ingham NJ
Year: 2019
Journal: PLoS Biol
Title: Mouse screen reveals multiple new genes underlying mouse and human hearing loss.
Volume: 17
Issue: 4
Pages: e3000194
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Publication
34321999 | J:313619
 
First Author: Bedogni F
Year: 2021
Journal: Front Mol Neurosci
Title: Cell-Type-Specific Gene Expression in Developing Mouse Neocortex: Intermediate Progenitors Implicated in Axon Development.
Volume: 14
Pages: 686034
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Publication
- | J:155845
     
First Author: Wellcome Trust Sanger Institute
Year: 2010
Journal: MGI Direct Data Submission
Title: Alleles produced for the EUCOMM and EUCOMMTools projects by the Wellcome Trust Sanger Institute
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Publication
- | J:211773
     
First Author: Mouse Genome Informatics and the International Mouse Phenotyping Consortium (IMPC)
Year: 2014
Journal: Database Release
Title: Obtaining and Loading Phenotype Annotations from the International Mouse Phenotyping Consortium (IMPC) Database
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Publication
- | J:157065
     
First Author: Helmholtz Zentrum Muenchen GmbH
Year: 2010
Journal: MGI Direct Data Submission
Title: Alleles produced for the EUCOMM and EUCOMMTools projects by the Helmholtz Zentrum Muenchen GmbH (Hmgu)
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Publication
- | J:155856
       
First Author: The Gene Ontology Consortium
Year: 2014
Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-rat orthologs
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Publication
- | J:342604
       
First Author: UniProt-GOA
Year: 2012
Title: Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
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Publication
16602821 | J:162220
First Author: Magdaleno S
Year: 2006
Journal: PLoS Biol
Title: BGEM: an in situ hybridization database of gene expression in the embryonic and adult mouse nervous system.
Volume: 4
Issue: 4
Pages: e86
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Publication
- | J:23000
       
First Author: MGD Nomenclature Committee
Year: 1995
Title: Nomenclature Committee Use
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Publication
- | J:293217
       
First Author: GemPharmatech
Year: 2020
Title: GemPharmatech Website.
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Publication
21677750 | J:173534
First Author: Skarnes WC
Year: 2011
Journal: Nature
Title: A conditional knockout resource for the genome-wide study of mouse gene function.
Volume: 474
Issue: 7351
Pages: 337-42
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Publication
- | J:342587
       
First Author: AgBase, BHF-UCL, Parkinson's UK-UCL, dictyBase, HGNC, Roslin Institute, FlyBase and UniProtKB curators
Year: 2011
Title: Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
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Publication
- | J:342605
       
First Author: GOA curators
Year: 2016
Title: Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
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Publication
- | J:164563
       
First Author: The Gene Ontology Consortium
Year: 2010
Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-human orthologs
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Publication
21267068 | J:153498
First Author: Diez-Roux G
Year: 2011
Journal: PLoS Biol
Title: A high-resolution anatomical atlas of the transcriptome in the mouse embryo.
Volume: 9
Issue: 1
Pages: e1000582
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Publication
- | J:157972
     
First Author: Mouse Genome Informatics Scientific Curators
Year: 2010
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome U74 Array Platform (A, B, C v2).
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Publication
- | J:57747
     
First Author: MGI Genome Annotation Group and UniGene Staff
Year: 2015
Journal: Database Download
Title: MGI-UniGene Interconnection Effort
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Publication
- | J:161428
       
First Author: Marc Feuermann, Huaiyu Mi, Pascale Gaudet, Dustin Ebert, Anushya Muruganujan, Paul Thomas
Year: 2010
Title: Annotation inferences using phylogenetic trees
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Publication
- | J:63103
     
First Author: Mouse Genome Database and National Center for Biotechnology Information
Year: 2000
Journal: Database Release
Title: Entrez Gene Load
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Publication
- | J:262123
     
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
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Publication
- | J:144086
     
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Gene 1.0 ST Array Platform
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Publication
- | J:155721
     
First Author: Mouse Genome Informatics (MGI) and The National Center for Biotechnology Information (NCBI)
Year: 2010
Journal: Database Download
Title: Consensus CDS project
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Publication
- | J:85324
     
First Author: Mouse Genome Informatics Group
Year: 2003
Journal: Database Procedure
Title: Automatic Encodes (AutoE) Reference
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Publication
- | J:53168
     
First Author: Bairoch A
Year: 1999
Journal: Database Release
Title: SWISS-PROT Annotated protein sequence database
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Publication
- | J:91388
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
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Publication
- | J:155221
     
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
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Publication
- | J:90438
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and loading genome assembly coordinates from NCBI annotations
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Publication
- | J:144087
     
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform
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Publication
19643958 | J:160432
First Author: Gibbs D
Year: 2010
Journal: Invest Ophthalmol Vis Sci
Title: Function of MYO7A in the human RPE and the validity of shaker1 mice as a model for Usher syndrome 1B.
Volume: 51
Issue: 2
Pages: 1130-5
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HT Experiment
GSE246143 | MYO7a is required for the functional integrity of the mechanoelectrical transduction complex in the outer hair cells of the adult cochlea.
 
Experiment Type: RNA-Seq
Study Type: WT vs. Mutant
Source: GEO
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GXD Expression
GXD Expression
Probe: MGI:5431536
Assay Type: Immunohistochemistry
Annotation Date: 2024-06-06
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1729022
Pattern: Regionally restricted
Stage: TS22
Assay Id: MGI:7645520
Age: embryonic day 14.0
Image: 3D
Note: Co-expression with Myo7a in hair cells.
Specimen Label: 3D
Detected: true
Specimen Num: 5
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GXD Expression
GXD Expression
Probe: MGI:5431536
Assay Type: Immunohistochemistry
Annotation Date: 2024-06-06
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1729022
Pattern: Regionally restricted
Stage: TS22
Assay Id: MGI:7645520
Age: embryonic day 14.0
Image: 3D
Note: Co-expression with Myo7a in hair cells.
Specimen Label: 3D
Detected: true
Specimen Num: 5
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GXD Expression
GXD Expression
Probe: MGI:6393603
Assay Type: Immunohistochemistry
Annotation Date: 2020-03-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1698217
Pattern: Regionally restricted
Stage: TS17
Assay Id: MGI:6393616
Age: embryonic day 10.5
Image: 2C inset
Note: Co-expression with Myo7a in cochleovestibular ganglion.
Specimen Label: 2C inset
Detected: true
Specimen Num: 4
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GXD Expression
GXD Expression
Probe: MGI:6393603
Assay Type: Immunohistochemistry
Annotation Date: 2020-03-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1698219
Pattern: Regionally restricted
Stage: TS19
Assay Id: MGI:6393616
Age: embryonic day 11.5
Image: 2I inset
Note: Co-expression with Myo7a in cochleovestibular ganglion.
Specimen Label: 2I inset
Detected: true
Specimen Num: 6
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GXD Expression
GXD Expression
Probe: MGI:1860227
Assay Type: Immunohistochemistry
Annotation Date: 2020-03-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1698217
Pattern: Regionally restricted
Stage: TS17
Assay Id: MGI:6393617
Age: embryonic day 10.5
Image: 2F inset
Note: Co-expression with Myo7a in cochleovestibular ganglion.
Specimen Label: 2F inset
Detected: true
Specimen Num: 4
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GXD Expression
GXD Expression
Probe: MGI:1860227
Assay Type: Immunohistochemistry
Annotation Date: 2020-03-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1698219
Pattern: Regionally restricted
Stage: TS19
Assay Id: MGI:6393617
Age: embryonic day 11.5
Image: 2L inset
Note: Co-expression with Myo7a in cochleovestibular ganglion.
Specimen Label: 2L inset
Detected: true
Specimen Num: 6
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GXD Expression
GXD Expression
Probe: MGI:6393608
Assay Type: Immunohistochemistry
Annotation Date: 2020-03-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1698217
Pattern: Regionally restricted
Stage: TS17
Assay Id: MGI:6393618
Age: embryonic day 10.5
Image: 4C inset
Note: Co-expression with Myo7a in cochleovestibular ganglion.
Specimen Label: 4C inset
Detected: true
Specimen Num: 2
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GXD Expression
GXD Expression
Probe: MGI:6393603
Assay Type: Immunohistochemistry
Annotation Date: 2020-03-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1666015
Pattern: Regionally restricted
Stage: TS15
Assay Id: MGI:6393616
Age: embryonic day 9.5
Image: 1C inset
Note: Co-expression with Myo7a in cochleovestibular ganglion.
Specimen Label: 1C inset
Detected: true
Specimen Num: 2
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GXD Expression
GXD Expression
Probe: MGI:1860227
Assay Type: Immunohistochemistry
Annotation Date: 2020-03-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1666015
Pattern: Regionally restricted
Stage: TS15
Assay Id: MGI:6393617
Age: embryonic day 9.5
Image: 1F inset
Note: Co-expression with Myo7a in cochleovestibular ganglion.
Specimen Label: 1F inset
Detected: true
Specimen Num: 2
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GXD Expression
GXD Expression
Probe: MGI:1860227
Assay Type: Immunohistochemistry
Annotation Date: 2020-03-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1757320
Pattern: Regionally restricted
Stage: TS20
Assay Id: MGI:6393617
Age: embryonic day 12.5
Image: 3C inset
Note: Co-expression with Myo7a in vestibular ganglion.
Specimen Label: 3C inset
Detected: true
Specimen Num: 8
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Publication
21936790 | -
First Author: Williams DS
Year: 2011
Journal: Biochem Soc Trans
Title: The many different cellular functions of MYO7A in the retina.
Volume: 39
Issue: 5
Pages: 1207-10
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GXD Expression
GXD Expression
 
Probe: MGI:7354987
Assay Type: Immunohistochemistry
Annotation Date: 2022-10-19
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1906128
Pattern: Regionally restricted
Stage: TS28
Assay Id: MGI:7356365
Age: postnatal day 28
Note: Co-expression with Myo7a in cytoplasm of hair cells.
Specimen Label: 6A/C
Detected: true
Specimen Num: 26
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GXD Expression
GXD Expression
 
Probe: MGI:7354987
Assay Type: Immunohistochemistry
Annotation Date: 2022-10-19
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1906128
Pattern: Regionally restricted
Stage: TS28
Assay Id: MGI:7356365
Age: postnatal day 28
Note: Co-expression with Myo7a in cytoplasm of hair cells.
Specimen Label: 6A/C
Detected: true
Specimen Num: 26
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Allele
Myo7a<dmbo2> | MGI:5487403
 
Name: myosin VIIA; dumbo2
Allele Type: Chemically induced (ENU)
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Genotype
Genotype
Symbol: Myo7a/Myo7a
Background: involves: C57BL/6J
Zygosity: hm
Has Mutant Allele: true
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DO Term
DOID:0110477 | autosomal recessive nonsyndromic deafness 2
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GXD Expression
GXD Expression
Probe: MGI:6393608
Assay Type: Immunohistochemistry
Annotation Date: 2020-03-10
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1698219
Pattern: Regionally restricted
Stage: TS19
Assay Id: MGI:6393618
Age: embryonic day 11.5
Image: 4F inset
Note: Co-expression with Myo7a in subset of Neurod1-expressing cells in cochleovestibular ganglion.
Specimen Label: 4F inset
Detected: true
Specimen Num: 4
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GXD Expression
GXD Expression
Probe: MGI:5431536
Assay Type: Immunohistochemistry
Annotation Date: 2024-06-06
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3524723
Pattern: Regionally restricted
Stage: TS23
Assay Id: MGI:7645520
Age: embryonic day 15.0
Image: 5B
Note: Co expression with Myo7a in subset of cells within zone of proliferating cells (ZNP"C) at basal end.
Specimen Label: 5B
Detected: true
Specimen Num: 8
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GXD Expression
GXD Expression
 
Probe: MGI:7354987
Assay Type: Immunohistochemistry
Annotation Date: 2022-10-19
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1906127
Pattern: Regionally restricted
Stage: TS27
Assay Id: MGI:7356365
Age: postnatal day 1
Note: Expression in organ of Corti in both cytoplasm and nucleus of inner cells and outer hair cells, co-expressed with Myo7a
Specimen Label: 2C
Detected: true
Specimen Num: 12
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GXD Expression
GXD Expression
 
Probe: MGI:7354987
Assay Type: Immunohistochemistry
Annotation Date: 2022-10-19
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1906127
Pattern: Regionally restricted
Stage: TS27
Assay Id: MGI:7356365
Age: postnatal day 1
Note: Expression in organ of Corti in both cytoplasm and nucleus of inner cells and outer hair cells, co-expressed with Myo7a
Specimen Label: 2C
Detected: true
Specimen Num: 12
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Allele
Myo7a<sh1-6R> | MGI:3622651
 
Name: myosin VIIA; shaker 1, 6 Oak Ridge
Allele Type: Chemically induced (ENU)
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Allele
Hprt1<tm2Brd> | MGI:3776895
Name: hypoxanthine phosphoribosyltransferase 1; targeted mutation 2, Allan Bradley
Allele Type: Targeted
Attribute String: Null/knockout, Reporter
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DO Term
DOID:0110543 | autosomal dominant nonsyndromic deafness 11
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Allele
Myo7a<Hdb> | MGI:3511858
 
Name: myosin VIIA; headbanger
Allele Type: Chemically induced (ENU)
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Strain
MGI:5561057 | C3;129S7-Hprt1<tm2Brd>/Biat
Attribute String: targeted mutation
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Strain
MGI:5491884 | C3HeB/FeJ-Myo7a<Hdb>/Ieg
Attribute String: mutant strain, coisogenic, chemically induced mutation
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Genotype
Genotype
Symbol: Myo7a/Myo7a
Background: C3HeB/FeJ-Myo7a/Ieg
Zygosity: hm
Has Mutant Allele: true
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Genotype
Genotype
Symbol: Myo7a/Myo7a<+>
Background: C3HeB/FeJ-Myo7a/Ieg
Zygosity: ht
Has Mutant Allele: true
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Publication
12588794 | J:82023
First Author: Weil D
Year: 2003
Journal: Hum Mol Genet
Title: Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin.
Volume: 12
Issue: 5
Pages: 463-71
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Publication
20142502 | -
First Author: Yan J
Year: 2010
Journal: Proc Natl Acad Sci U S A
Title: The structure of the harmonin/sans complex reveals an unexpected interaction mode of the two Usher syndrome proteins.
Volume: 107
Issue: 9
Pages: 4040-5
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Publication
24608321 | J:210992
First Author: Bauß K
Year: 2014
Journal: Hum Mol Genet
Title: Phosphorylation of the Usher syndrome 1G protein SANS controls Magi2-mediated endocytosis.
Volume: 23
Issue: 15
Pages: 3923-42
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