No title available.Shi N.-Q., Ye B., Kroboth S.L., McNally E., Makielski J.M.Cited forNUCLEOTIDE SEQUENCEStrainFVBTissueHeartCategorySequencesSourceUniProtKB unreviewed (TrEMBL)Submission Submitted to EMBL/GenBank/DDBJ databases (SEP-2006)Cited in2
Molecular identification and functional characterization of a mitochondrial sulfonylurea receptor 2 splice variant generated by intraexonic splicing.Ye B., Kroboth S.L., Pu J.L., Sims J.J., Aggarwal N.T., McNally E.M., Makielski J.C., Shi N.Q.View abstractCited forNUCLEOTIDE SEQUENCEStrainFVBTissueHeartCategorySequencesSourceUniProtKB unreviewed (TrEMBL)PubMedEurope PMCCirc Res 105:1083-1093 (2009)Cited in2Mapped to4
Cloning and characterization of a novel class II phosphoinositide 3-kinase containing C2 domain.Misawa H., Ohtsubo M., Copeland N.G., Gilbert D.J., Jenkins N.A., Yoshimura A.View abstractCategorySequencesSourceMGI: 1352630PubMedEurope PMCBiochem. Biophys. Res. Commun. 244:531-539 (1998)Cited in1Mapped to48
Sur2 and Kcnj8 genes are tightly linked on the distal region of mouse chromosome 6.Isomoto S., Horio Y., Matsumoto S., Kondo C., Yamada M., Gilbert D.J., Copeland N.G., Jenkins N.A., Kurachi Y.CategorySequencesSourceMGI: 1352630PubMedEurope PMCMamm Genome 8:790-791 (1997)Mapped to24
Sulphonylurea receptor 2B and Kir6.1 form a sulphonylurea-sensitive but ATP-insensitive K+ channel.Yamada M., Isomoto S., Matsumoto S., Kondo C., Shindo T., Horio Y., Kurachi Y.View abstractCategoriesFunction, SequencesSourceMGI: 1352630PubMedEurope PMCJ. Physiol. (Lond. ) 499:715-720 (1997)Cited in1Mapped to13
A novel sulfonylurea receptor forms with BIR (Kir6.2) a smooth muscle type ATP-sensitive K+ channel.Isomoto S., Kondo C., Yamada M., Matsumoto S., Higashiguchi O., Horio Y., Matsuzawa Y., Kurachi Y.View abstractCategorySequencesSourceMGI: 1352630PubMedEurope PMCJ. Biol. Chem. 271:24321-24324 (1996)Cited in2Mapped to25
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 abstractCategoryFunctionSourceMGI: 1352630PubMedEurope PMCNature 627:130-136 (2024)Mapped to99+
Wnt signaling regulates ion channel expression to promote smooth muscle and cartilage formation in developing mouse trachea.Russell N.X., Burra K., Shah R.M., Bottasso-Arias N., Mohanakrishnan M., Snowball J., Ediga H.H., Madala S.K., Sinner D.View abstractCategoryFunctionSourceMGI: 1352630PubMedEurope PMCAm J Physiol Lung Cell Mol Physiol 325:L788-L802 (2023)Mapped to99+
Skeletal muscle delimited myopathy and verapamil toxicity in SUR2 mutant mouse models of AIMS.McClenaghan C., Mukadam M.A., Roeglin J., Tryon R.C., Grabner M., Dayal A., Meyer G.A., Nichols C.G.View abstractSourceMGI: 1352630PubMedEurope PMCEMBO Mol Med 15:e16883-e16883 (2023)Mapped to14
KCNJ8/ABCC9-containing K-ATP channel modulates brain vascular smooth muscle development and neurovascular coupling.Ando K., Tong L., Peng D., Vazquez-Liebanas E., Chiyoda H., He L., Liu J., Kawakami K., Mochizuki N.[...], Betsholtz C.View abstractCategoryFunctionSourceMGI: 1352630PubMedEurope PMCDev Cell 57:1383-1399.e7 (2022)Mapped to9
Consequences of SUR2[A478V] Mutation in Skeletal Muscle of Murine Model of Cantu Syndrome.Scala R., Maqoud F., Zizzo N., Passantino G., Mele A., Camerino G.M., McClenaghan C., Harter T.M., Nichols C.G., Tricarico D.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 1352630PubMedEurope PMCCells 10:1791-1791 (2021)Mapped to6
Complex consequences of Cantu syndrome SUR2 variant R1154Q in genetically modified mice.Zhang H., Hanson A., de Almeida T.S., Emfinger C., McClenaghan C., Harter T., Yan Z., Cooper P.E., Brown G.S.[...], Nichols C.G.View abstractCategorySequencesSourceMGI: 1352630PubMedEurope PMCJCI Insight 6:145934-145934 (2021)Mapped to16
The Metabolic Reprogramming of <i>Frem2</i> Mutant Mice Embryos in Cryptophthalmos Development.Zhang X., Wang R., Wang T., Zhang X., Dongye M., Wang D., Wang J., Li W., Wu X.[...], Lin H.View abstractCategoriesFunction, ExpressionSourceMGI: 1352630PubMedEurope PMCFront Cell Dev Biol 8:625492-625492 (2020)Mapped to45
Kir6.1- and SUR2-dependent KATP overactivity disrupts intestinal motility in murine models of Cantu syndrome.York N.W., Parker H., Xie Z., Tyus D., Waheed M.A., Yan Z., Grange D.K., Remedi M.S., England S.K.[...], Nichols C.G.View abstractCategoryPhenotypes & VariantsSourceMGI: 1352630PubMedEurope PMCJCI Insight 5:e141443-e141443 (2020)Mapped to9
Improved adaptation to physical stress in mice overexpressing SUR2A is associated with changes in the pattern of Q-T interval.Sudhir R., Du Q., Sukhodub A., Jovanovic S., Jovanovic A.View abstractCategoryFunctionSourceMGI: 1352630PubMedEurope PMCPflugers Arch 472:683-691 (2020)Mapped to6
Kir6.1-dependent K<sub>ATP</sub> channels in lymphatic smooth muscle and vessel dysfunction in mice with Kir6.1 gain-of-function.Davis M.J., Kim H.J., Zawieja S.D., Castorena-Gonzalez J.A., Gui P., Li M., Saunders B.T., Zinselmeyer B.H., Randolph G.J.[...], Nichols C.G.View abstractSourceMGI: 1352630PubMedEurope PMCJ Physiol 598:3107-3127 (2020)Mapped to10
Glibenclamide reverses cardiovascular abnormalities of Cantu syndrome driven by KATP channel overactivity.McClenaghan C., Huang Y., Yan Z., Harter T.M., Halabi C.M., Chalk R., Kovacs A., van Haaften G., Remedi M.S., Nichols C.G.View abstractCategorySequencesSourceMGI: 1352630PubMedEurope PMCJ Clin Invest 130:1116-1121 (2020)Mapped to9
ABCC9-related Intellectual disability Myopathy Syndrome is a KATP channelopathy with loss-of-function mutations in ABCC9.Smeland M.F., McClenaghan C., Roessler H.I., Savelberg S., Hansen G.A.M., Hjellnes H., Arntzen K.A., Mueller K.I., Dybesland A.R.[...], van Haaften G.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 1352630PubMedEurope PMCNat. Commun. 10:4457-4457 (2019)Cited in1Mapped to14
Cardiovascular consequences of KATP overactivity in Cantu syndrome.Huang Y., McClenaghan C., Harter T.M., Hinman K., Halabi C.M., Matkovich S.J., Zhang H., Brown G.S., Mecham R.P.[...], Nichols C.G.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 1352630PubMedEurope PMCJCI Insight 3:121153-121153 (2018)Mapped to9
Extensive alternative splicing transitions during postnatal skeletal muscle development are required for calcium handling functions.Brinegar A.E., Xia Z., Loehr J.A., Li W., Rodney G.G., Cooper T.A.View abstractCategoriesFunction, ExpressionSourceMGI: 1352630PubMedEurope PMCElife 6:e27192-e27192 (2017)Mapped to99+
A subset of cerebrovascular pericytes originates from mature macrophages in the very early phase of vascular development in CNS.Yamamoto S., Muramatsu M., Azuma E., Ikutani M., Nagai Y., Sagara H., Koo B.N., Kita S., O'Donnell E.[...], Sasahara M.View abstractCategoryExpressionSourceMGI: 1352630PubMedEurope PMCSci Rep 7:3855-3855 (2017)Mapped to97
Muscle developmental defects in heterogeneous nuclear Ribonucleoprotein A1 knockout mice.Liu T.Y., Chen Y.C., Jong Y.J., Tsai H.J., Lee C.C., Chang Y.S., Chang J.G., Chang Y.F.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 1352630PubMedEurope PMCOpen Biol 7:160303-160303 (2017)Mapped to99+
Reprogramming of Sertoli cells to fetal-like Leydig cells by Wt1 ablation.Zhang L., Chen M., Wen Q., Li Y., Wang Y., Wang Y., Qin Y., Cui X., Yang L.[...], Gao F.View abstractCategoryExpressionSourceMGI: 1352630PubMedEurope PMCProc Natl Acad Sci U S A 112:4003-4008 (2015)Mapped to99+
Mild hypoxia in vivo regulates cardioprotective SUR2A: A role for Akt and LDH.Mohammed Abdul K.S., Jovanovic S., Du Q., Sukhodub A., Jovanovic A.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 1352630PubMedEurope PMCBiochim Biophys Acta 1852:709-719 (2015)Mapped to33
RBM24 is a major regulator of muscle-specific alternative splicing.Yang J., Hung L.H., Licht T., Kostin S., Looso M., Khrameeva E., Bindereif A., Schneider A., Braun T.View abstractCategoriesFunction, SequencesSourceMGI: 1352630PubMedEurope PMCDev. Cell 31:87-99 (2014)Cited in2Mapped to50