A type VII myosin encoded by the mouse deafness gene shaker-1.Gibson F., Walsh J., Mburu P., Varela A., Brown K.A., Antonio M., Beisel K.W., Steel K.P., Brown S.D.M.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1), DISEASECategoriesSequences, Phenotypes & VariantsSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNature 374:62-64 (1995)Cited in1Mapped to10
Mutation analysis of the mouse myosin VIIA deafness gene.Mburu P., Liu X.-Z., Walsh J., Saw D. Jr., Cope M.J., Gibson F., Kendrick-Jones J., Steel K.P., Brown S.D.M.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1)CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCGenes Funct. 1:191-203 (1997)Cited in1Mapped to7
Lineage-specific biology revealed by a finished genome assembly of the mouse.Church D.M., Goodstadt L., Hillier L.W., Zody M.C., Goldstein S., She X., Bult C.J., Agarwala R., Cherry J.L.[...], Ponting C.P.View abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]StrainC57BL/6JCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCPLoS Biol. 7:E1000112-E1000112 (2009)Cited in99+99+
Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia.Belyantseva I.A., Boger E.T., Naz S., Frolenkov G.I., Sellers J.R., Ahmed Z.M., Griffith A.J., Friedman T.B.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] OF 12-2215 (ISOFORM 2), TISSUE SPECIFICITYStrainC57BL/6JTissueInner earCategoriesSequences, ExpressionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNat. Cell Biol. 7:148-156 (2005)Cited in3Mapped to14
Slac2-c (synaptotagmin-like protein homologue lacking C2 domains-c), a novel linker protein that interacts with Rab27, myosin Va/VIIa, and actin.Fukuda M., Kuroda T.S.View abstractCited forINTERACTION WITH MYRIPCategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Biol. Chem. 277:43096-43103 (2002)Cited in5Mapped to27
Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly.Delprat B., Michel V., Goodyear R., Yamasaki Y., Michalski N., El-Amraoui A., Perfettini I., Legrain P., Richardson G.[...], Petit C.View abstractCited forINTERACTION WITH WHRNCategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCHum. Mol. Genet. 14:401-410 (2005)Cited in3Mapped to18
PHR1, an integral membrane protein of the inner ear sensory cells, directly interacts with myosin 1c and myosin VIIa.Etournay R., El-Amraoui A., Bahloul A., Blanchard S., Roux I., Pezeron G., Michalski N., Daviet L., Hardelin J.-P.[...], Petit C.View abstractCited forINTERACTION WITH PLEKHB1CategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Cell Sci. 118:2891-2899 (2005)Cited in3Mapped to19
Physical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cells.Senften M., Schwander M., Kazmierczak P., Lillo C., Shin J.B., Hasson T., Geleoc G.S., Gillespie P.G., Williams D.[...], Muller U.View abstractCited forINTERACTION WITH PCDH15CategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Neurosci. 26:2060-2071 (2006)Cited in2Mapped to30
Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning.Michalski N., Michel V., Bahloul A., Lefevre G., Barral J., Yagi H., Chardenoux S., Weil D., Martin P.[...], Petit C.View abstractCited forINTERACTION WITH ADGRV1 AND USH2ACategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Neurosci. 27:6478-6488 (2007)Cited in6Mapped to74
MyosinVIIa interacts with Twinfilin-2 at the tips of mechanosensory stereocilia in the inner ear.Rzadzinska A.K., Nevalainen E.M., Prosser H.M., Lappalainen P., Steel K.P.View abstractCited forINTERACTION WITH TWF2StrainC3Heb/FeJTissueInner earCategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCPLoS ONE 4:E7097-E7097 (2009)Cited in2Mapped to2
A tissue-specific atlas of mouse protein phosphorylation and expression.Huttlin E.L., Jedrychowski M.P., Elias J.E., Goswami T., Rad R., Beausoleil S.A., Villen J., Haas W., Sowa M.E., Gygi S.P.View abstractCited forPHOSPHORYLATION [LARGE SCALE ANALYSIS] AT THR-1563; SER-1569 AND THR-1571, IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS]TissueKidney, TestisCategoriesPTM / Processing, SequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCCell 143:1174-1189 (2010)Cited in99+99+Mapped to6
The Usher 1B protein, MYO7A, is required for normal localization and function of the visual retinoid cycle enzyme, RPE65.Lopes V.S., Gibbs D., Libby R.T., Aleman T.S., Welch D.L., Lillo C., Jacobson S.G., Radu R.A., Steel K.P., Williams D.S.View abstractCited forFUNCTION, TISSUE SPECIFICITY, INTERACTION WITH RPE65CategoriesFunction, Expression, InteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCHum. Mol. Genet. 20:2560-2570 (2011)Cited in3Mapped to10
Myosin VIIa and sans localization at stereocilia upper tip-link density implicates these Usher syndrome proteins in mechanotransduction.Grati M., Kachar B.View abstractCited forFUNCTION, TISSUE SPECIFICITY, SUBCELLULAR LOCATIONCategoriesFunction, Expression, Subcellular LocationSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 108:11476-11481 (2011)Cited in5Mapped to51
PDZD7-MYO7A complex identified in enriched stereocilia membranes.Morgan C.P., Krey J.F., Grati M., Zhao B., Fallen S., Kannan-Sundhari A., Liu X.Z., Choi D., Mueller U., Barr-Gillespie P.G.View abstractCited forINTERACTION WITH PDZD7, FUNCTION, SUBCELLULAR LOCATIONCategoriesFunction, Interaction, Subcellular LocationSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCElife 5:0-0 (2016)Cited in3Mapped to10
The E3 ligase Ubr3 regulates Usher syndrome and MYH9 disorder proteins in the auditory organs of Drosophila and mammals.Li T., Giagtzoglou N., Eberl D.F., Jaiswal S.N., Cai T., Godt D., Groves A.K., Bellen H.J.View abstractCited forINTERACTION WITH MYH9CategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCElife 5:E15258-E15258 (2016)Cited in12Mapped to19
Structure of MyTH4-FERM domains in myosin VIIa tail bound to cargo.Wu L., Pan L., Wei Z., Zhang M.View abstractCited forX-RAY CRYSTALLOGRAPHY (2.8 ANGSTROMS) OF 965-1687 IN COMPLEX WITH USH1G, INTERACTION WITH USH1G, MUTAGENESIS OF ALA-1189 AND PHE-1473CategoriesInteraction, Phenotypes & Variants, StructureSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCScience 331:757-760 (2011)Cited in2Mapped to3
Genomics and hearing impairment.Keats B.J., Berlin C.I.View abstractCategoriesSequencesSourceMGI: 104510PubMedEurope PMCGenome Res 9:7-16 (1999)Mapped to35
Requirement for Brn-3c in maturation and survival, but not in fate determination of inner ear hair cells.Xiang M., Gao W.Q., Hasson T., Shin J.J.View abstractCategoriesExpressionSourceMGI: 104510PubMedEurope PMCDevelopment 125:3935-3946 (1998)Mapped to28
Mutant myosin VIIa causes defective melanosome distribution in the RPE of shaker-1 mice.Liu X., Ondek B., Williams D.S.CategoriesFunctionSourceMGI: 104510PubMedEurope PMCNat Genet 19:117-118 (1998)Mapped to8
Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells.Self T., Mahony M., Fleming J., Walsh J., Brown S.D., Steel K.P.View abstractCategoriesPhenotypes & VariantsSourceMGI: 104510PubMedEurope PMCDevelopment 125:557-566 (1998)Mapped to8
Unconventional myosins, the basis for deafness in mouse and man.Hasson T.CategoriesFunction, SequencesSourceMGI: 104510PubMedEurope PMCAm J Hum Genet 61:801-805 (1997)Mapped to8
Expression of myosin VIIA during mouse embryogenesis.Sahly I., El-Amraoui A., Abitbol M., Petit C., Dufier J.L.View abstractCategoriesSequences, ExpressionSourceMGI: 104510PubMedEurope PMCAnat Embryol (Berl) 196:159-170 (1997)Mapped to8
Effects of shaker-1 mutations on myosin-VIIa protein and mRNA expression.Hasson T., Walsh J., Cable J., Mooseker M.S., Brown S.D., Steel K.P.View abstractCategoriesSequencesSourceMGI: 104510PubMedEurope PMCCell Motil Cytoskeleton 37:127-138 (1997)Mapped to8
Mutations in the myosin VIIA gene cause non-syndromic recessive deafness.Liu X.-Z., Walsh J., Mburu P., Kendrick-Jones J., Cope M.J., Steel K.P., Brown S.D.M.View abstractCategoriesSequencesSourceMGI: 104510PubMedEurope PMCNat. Genet. 16:188-190 (1997)Cited in1Mapped to8
Shaker mice and a peek into the House of Usher.Saw D. Jr., Steel K.P., Brown S.D.CategoriesFunctionSourceMGI: 104510PubMedEurope PMCExp Anim 46:1-9 (1997)Mapped to8