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/6JCategorySequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCPLoS Biol. 7:E1000112-E1000112 (2009)Cited in99+99+
Modernizing reference genome assemblies.Church D.M., Schneider V.A., Graves T., Auger K., Cunningham F., Bouk N., Chen H.C., Agarwala R., McLaren W.M.[...], Hubbard T.Cited forNUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]StrainC57BL/6JCategorySequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCPLoS Biol 9:e1001091-e1001091 (2011)Cited in99+
No title available.EnsemblCited forIDENTIFICATIONStrainC57BL/6JSourceUniProtKB unreviewed (TrEMBL)Submission Submitted to UniProtKB (AUG-2024)Cited in99+
Linkage analysis of the whirler deafness gene on mouse chromosome 4.Fleming J., Rogers M.J., Brown S.D., Steel K.P.View abstractCategorySequencesSourceMGI: 2682003PubMedEurope PMCGenomics 21:42-48 (1994)Mapped to30
Molecular genetics of the brown (b)-locus region of mouse chromosome 4. II. Complementation analyses of lethal brown deletions.Rinchik E.M.View abstractCategorySequencesSourceMGI: 2682003PubMedEurope PMCGenetics 137:855-865 (1994)Mapped to15
Molecular genetics of the brown (b)-locus region of mouse chromosome 4. I. Origin and molecular mapping of radiation- and chemical-induced lethal brown deletions.Rinchik E.M., Bell J.A., Hunsicker P.R., Friedman J.M., Jackson I.J., Russell L.B.View abstractCategorySequencesSourceMGI: 2682003PubMedEurope PMCGenetics 137:845-854 (1994)Mapped to18
Metabolic and endocrine differences between the mutation whirler and normal female mice.Sackler A.M., Weltman A.S.CategoryFunctionSourceMGI: 2682003PubMedEurope PMCJ Exp Zool 164:133-140 (1967)Mapped to11
Metabolism rate, biochemical and endocrine alterations in male whirler mice.Weltman A.S., Sackler A.M., Lewis A.S., Johnson L.CategoryFunctionSourceMGI: 2682003PubMedEurope PMCPhysiol Behav 5:17-22 (1970)Mapped to6
Pleiotropic brain function of whirlin identified by a novel mutation.Aguilar C., Williams D., Kurapati R., Bains R.S., Mburu P., Parker A., Williams J., Concas D., Tateossian H.[...], Lad H.V.View abstractCategoryFunctionSourceMGI: 2682003PubMedEurope PMCiScience 27:110170-110170 (2024)Mapped to6
Genetic determinants of micronucleus formation in vivo.Adams D.J., Barlas B., McIntyre R.E., Salguero I., van der Weyden L., Barros A., Vicente J.R., Karimpour N., Haider A.[...], White J.K.View abstractCategoriesNames, Family & DomainsSourceMGI: 2682003PubMedEurope PMCNature 627:130-136 (2024)Mapped to99+
Deafness-Associated ADGRV1 Mutation Impairs USH2A Stability through Improper Phosphorylation of WHRN and WDSUB1 Recruitment.Guan Y., Du H.B., Yang Z., Wang Y.Z., Ren R., Liu W.W., Zhang C., Zhang J.H., An W.T.[...], Xu Z.G.View abstractCategoryFunctionSourceMGI: 2682003PubMedEurope PMCAdv Sci (Weinh) 10:e2205993-e2205993 (2023)Mapped to26
RGS12 polarizes the GPSM2-GNAI complex to organize and elongate stereocilia in sensory hair cells.Akturk A., Day M., Tarchini B.View abstractCategoryFunctionSourceMGI: 2682003PubMedEurope PMCSci Adv 8:eabq2826-eabq2826 (2022)Mapped to83
Interaction of protocadherin-15 with the scaffold protein whirlin supports its anchoring of hair-bundle lateral links in cochlear hair cells.Michel V., Pepermans E., Boutet de Monvel J., England P., Nouaille S., Aghaie A., Delhommel F., Wolff N., Perfettini I.[...], Bahloul A.View abstractCategoryInteractionSourceMGI: 2682003PubMedEurope PMCSci Rep 10:16430-16430 (2020)Mapped to31
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss.Collin G.B., Gogna N., Chang B., Damkham N., Pinkney J., Hyde L.F., Stone L., Naggert J.K., Nishina P.M., Krebs M.P.View abstractCategoryNamesSourceMGI: 2682003PubMedEurope PMCCells 9:E931-E931 (2020)Mapped to99+
Impact of Auditory Experience on the Structural Plasticity of the AIS in the Mouse Brainstem Throughout the Lifespan.Kim E.J., Feng C., Santamaria F., Kim J.H.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 2682003PubMedEurope PMCFront Cell Neurosci 13:456-456 (2019)Mapped to6
Clarin-2 is essential for hearing by maintaining stereocilia integrity and function.Dunbar L.A., Patni P., Aguilar C., Mburu P., Corns L., Wells H.R., Delmaghani S., Parker A., Johnson S.[...], Bowl M.R.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 2682003PubMedEurope PMCEMBO Mol. Med. 11:e10288-e10288 (2019)Cited in1Mapped to66
Mouse screen reveals multiple new genes underlying mouse and human hearing loss.Ingham N.J., Pearson S.A., Vancollie V.E., Rook V., Lewis M.A., Chen J., Buniello A., Martelletti E., Preite L.[...], Steel K.P.View abstractCategoryFunctionSourceMGI: 2682003PubMedEurope PMCPLoS Biol. 17:E3000194-E3000194 (2019)Cited in4Mapped to99+
GPSM2-GNAI Specifies the Tallest Stereocilia and Defines Hair Bundle Row Identity.Tadenev A.L.D., Akturk A., Devanney N., Mathur P.D., Clark A.M., Yang J., Tarchini B.View abstractCategoriesFunction, ExpressionSourceMGI: 2682003PubMedEurope PMCCurr Biol 29:921-934.e4 (2019)Mapped to38
Ablation of cytoskeletal scaffolding proteins, Band 4.1B and Whirlin, leads to cerebellar purkinje axon pathology and motor dysfunction.Saifetiarova J., Bhat M.A.View abstractSourceMGI: 2682003PubMedEurope PMCJ Neurosci Res 97:313-331 (2019)Mapped to26
CIB2 interacts with TMC1 and TMC2 and is essential for mechanotransduction in auditory hair cells.Giese A.P.J., Tang Y.Q., Sinha G.P., Bowl M.R., Goldring A.C., Parker A., Freeman M.J., Brown S.D.M., Riazuddin S.[...], Ahmed Z.M.View abstractCategoriesFunction, InteractionSourceMGI: 2682003PubMedEurope PMCNat. Commun. 8:43-43 (2017)Cited in5Mapped to48
Defective Gpsm2/Galphapisub>i3pi/sub> signalling disrupts stereocilia development and growth cone actin dynamics in Chudley-McCullough syndrome.Mauriac S.A., Hien Y.E., Bird J.E., Carvalho S.D., Peyroutou R., Lee S.C., Moreau M.M., Blanc J.M., Geyser A.[...], Montcouquiol M.View abstractCategoryFunctionSourceMGI: 2682003PubMedEurope PMCNat Commun 8:14907-14907 (2017)Mapped to14
The roles of USH1 proteins and PDZ domain-containing USH proteins in USH2 complex integrity in cochlear hair cells.Zou J., Chen Q., Almishaal A., Mathur P.D., Zheng T., Tian C., Zheng Q.Y., Yang J.View abstractCategoryInteractionSourceMGI: 2682003PubMedEurope PMCHum Mol Genet 26:624-636 (2017)Mapped to38
Novel gene function revealed by mouse mutagenesis screens for models of age-related disease.Potter P.K., Bowl M.R., Jeyarajan P., Wisby L., Blease A., Goldsworthy M.E., Simon M.M., Greenaway S., Michel V.[...], Brown S.D.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 2682003PubMedEurope PMCNat Commun 7:12444-12444 (2016)Mapped to99+
Alternative Splice Forms Influence Functions of Whirlin in Mechanosensory Hair Cell Stereocilia.Ebrahim S., Ingham N.J., Lewis M.A., Rogers M.J.C., Cui R., Kachar B., Pass J.C., Steel K.P.View abstractCategoryExpressionSourceMGI: 2682003PubMedEurope PMCCell Rep 15:935-943 (2016)Mapped to9
Whirlin increases TRPV1 channel expression and cellular stability.Ciardo M.G., Andres-Borderia A., Cuesta N., Valente P., Camprubi-Robles M., Yang J., Planells-Cases R., Ferrer-Montiel A.View abstractCategoryInteractionSourceMGI: 2682003PubMedEurope PMCBiochim Biophys Acta 1863:115-127 (2016)Mapped to15