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 reviewed (Swiss-Prot)PubMedEurope PMCPLoS Biol. 7:E1000112-E1000112 (2009)Cited in99+99+
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 forIDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS]CategorySequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCCell 143:1174-1189 (2010)Cited in99+99+Mapped to6
Neuronal death and perinatal lethality in voltage-gated sodium channel alpha(II)-deficient mice.Planells-Cases R., Caprini M., Zhang J., Rockenstein E.M., Rivera R.R., Murre C., Masliah E., Montal M.View abstractCited forDISRUPTION PHENOTYPE, FUNCTION, TRANSPORTER ACTIVITY, TISSUE SPECIFICITY, SUBCELLULAR LOCATIONCategoriesFunction, Expression, Phenotypes & Variants, Subcellular LocationSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCBiophys. J. 78:2878-2891 (2000)Cited in2Mapped to19
A gain-of-function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities.Kearney J.A., Plummer N.W., Smith M.R., Kapur J., Cummins T.R., Waxman S.G., Goldin A.L., Meisler M.H.View abstractCited forFUNCTION, TRANSPORTER ACTIVITY, MUTAGENESIS OF 880-VAL--ALA-882, TISSUE SPECIFICITYCategoriesFunction, Expression, Phenotypes & VariantsSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNeuroscience 102:307-317 (2001)Cited in2
CaMKII modulates sodium current in neurons from epileptic Scn2a mutant mice.Thompson C.H., Hawkins N.A., Kearney J.A., George A.L. Jr.View abstractCited forFUNCTION, TRANSPORTER ACTIVITY, MUTAGENESIS OF 880-VAL--ALA-882CategoriesFunction, Phenotypes & VariantsSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 114:1696-1701 (2017)Cited in1Mapped to6
Altered hippocampal replay is associated with memory impairment in mice heterozygous for the Scn2a gene.Middleton S.J., Kneller E.M., Chen S., Ogiwara I., Montal M., Yamakawa K., McHugh T.J.View abstractCited forFUNCTIONCategoryFunctionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNat. Neurosci. 21:996-1003 (2018)Cited in1Mapped to12
Molecular cloning, characterization, and chromosomal localization of FKBP23, a novel FK506-binding protein with Ca2+-binding ability.Nakamura T., Yabe D., Kanazawa N., Tashiro K., Sasayama S., Honjo T.View abstractCategorySequencesSourceMGI: 98248PubMedEurope PMCGenomics 54:89-98 (1998)Cited in1Mapped to63
Confirmation of quantitative trait loci for alcohol preference in mice.Tarantino L.M., McClearn G.E., Rodriguez L.A., Plomin R.View abstractCategorySequencesSourceMGI: 98248PubMedEurope PMCAlcohol Clin Exp Res 22:1099-1105 (1998)Mapped to58
Use of recombinant inbred strains for studying genetic determinants of responses to alcohol.Crabbe J.C., Belknap J.K., Buck K.J., Metten P.View abstractCategoriesSequences, Phenotypes & VariantsSourceMGI: 98248PubMedEurope PMCAlcohol Alcohol Suppl 2:67-71 (1994)Mapped to37
A new sodium channel alpha-subunit gene (Scn9a) from Schwann cells maps to the Scn1a, Scn2a, Scn3a cluster of mouse chromosome 2.Beckers M.C., Ernst E., Belcher S., Howe J., Levenson R., Gros P.View abstractCategorySequencesSourceMGI: 98248PubMedEurope PMCGenomics 36:202-205 (1996)Mapped to54
DNA segments mapped by reciprocal use of microsatellite primers between mouse and rat.Kondo Y., Mori M., Kuramoto T., Yamada J., Beckmann J.S., Simon-Chazottes D., Montagutelli X., Guenet J.L., Serikawa T.View abstractCategorySequencesSourceMGI: 98248PubMedEurope PMCMamm Genome 4:571-576 (1993)Mapped to63
Quantitative trait loci mapping of genes that influence the sensitivity and tolerance to ethanol-induced hypothermia in BXD recombinant inbred mice.Crabbe J.C., Belknap J.K., Mitchell S.R., Crawshaw L.I.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 98248PubMedEurope PMCJ Pharmacol Exp Ther 269:184-192 (1994)Mapped to71
Dinucleotide repeats in the mouse Hox-4.4 and Hox-4.5 genes on chromosome 2, and their analysis in the BXD and BXH recombinant inbred strains.Pilz A.J., Abbott C.M.CategorySequencesSourceMGI: 98248PubMedEurope PMCMamm Genome 4:129-130 (1993)Mapped to15
A single linkage group comprising 11 polymorphic DNA markers on rat chromosome 3.Zha H., Remmers E.F., Du Y., Goldmuntz E.A., Mathern P., Zhang H., Cash J.M., Crofford L.J., Wilder R.L.View abstractCategorySequencesSourceMGI: 98248PubMedEurope PMCMamm Genome 5:538-541 (1994)Mapped to32
Aberrant hippocampal Ca<sup>2+</sup> microwaves following synapsin- dependent adeno-associated viral expression of Ca<sup>2+</sup> indicators.Masala N., Mittag M., Giovannetti E.A., O'Neil D.A., Distler F.J., Rupprecht P., Helmchen F., Yuste R., Fuhrmann M.[...], Kelly T.View abstractSourceMGI: 98248PubMedEurope PMCElife 13:RP93804-RP93804 (2024)Mapped to20
Experimental and computational evidence that Calpain-10 binds to the carboxy terminus of Na<sub>V</sub>1.2 and Na<sub>V</sub>1.6.Arratia L.M., Bermudes-Contreras J.D., Juarez-Monroy J.A., Romero-Macias E.A., Luna-Rojas J.C., Lopez-Hidalgo M., Vega A.V., Zamorano-Carrillo A.View abstractAnnotationExperimental and computational evidence that Calpain-10 binds to the carboxy terminus of NaV1.2 and NaV1.6.SourceGeneRif: 110876PubMedEurope PMCSci Rep 14:6761-6761 (2024)Mapped to20
Impaired cerebellar plasticity hypersensitizes sensory reflexes in SCN2A- associated ASD.Wang C., Derderian K.D., Hamada E., Zhou X., Nelson A.D., Kyoung H., Ahituv N., Bouvier G., Bender K.J.View abstractSourceMGI: 98248PubMedEurope PMCNeuron 112:1444-1455.e5 (2024)Mapped to13
Physical and functional convergence of the autism risk genes Scn2a and Ank2 in neocortical pyramidal cell dendrites.Nelson A.D., Catalfio A.M., Gupta J.P., Min L., Caballero-Floran R.N., Dean K.P., Elvira C.C., Derderian K.D., Kyoung H.[...], Jenkins P.M.View abstractAnnotationPhysical and functional convergence of the autism risk genes Scn2a and Ank2 in neocortical pyramidal cell dendrites.SourceGeneRif: 110876, MGI: 98248PubMedEurope PMCNeuron 112:1133-1149.e6 (2024)Mapped to31
Evaluating the interplay between estrous cyclicity and flurothyl-induced seizure susceptibility in <i>Scn2a <sup>K1422E</sup></i> mice.Echevarria-Cooper D.M., Kearney J.A.View abstractSourceMGI: 98248PubMedEurope PMCMicroPubl Biol 2023:0-0 (2023)Mapped to13
Dynamic Foraging Behavior Performance Is Not Affected by <i>Scn2a</i> Haploinsufficiency.Schamiloglu S., Wu H., Zhou M., Kwan A.C., Bender K.J.View abstractAnnotationDynamic Foraging Behavior Performance Is Not Affected by Scn2a Haploinsufficiency.CategoryFunctionSourceGeneRif: 110876PubMedEurope PMCeNeuro 10:ENEURO.0367-23.2023 (2023)Mapped to10
Inversed Effects of Nav1.2 Deficiency at Medial Prefrontal Cortex and Ventral Tegmental Area for Prepulse Inhibition in Acoustic Startle Response.Suzuki T., Hattori S., Mizukami H., Nakajima R., Hibi Y., Kato S., Matsuzaki M., Ikebe R., Miyakawa T., Yamakawa K.View abstractAnnotationInversed Effects of Nav1.2 Deficiency at Medial Prefrontal Cortex and Ventral Tegmental Area for Prepulse Inhibition in Acoustic Startle Response.SourceGeneRif: 110876PubMedEurope PMCMol Neurobiol 61:622-634 (2024)Mapped to10
Kv7/KCNQ potassium channels in cortical hyperexcitability and juvenile seizure-related death in Ank2-mutant mice.Oh H., Lee S., Oh Y., Kim S., Kim Y.S., Yang Y., Choi W., Yoo Y.E., Cho H.[...], Kim E.View abstractSourceMGI: 98248PubMedEurope PMCNat Commun 14:3547-3547 (2023)Mapped to99+
Cellular and behavioral effects of altered NaV1.2 sodium channel ion permeability in Scn2aK1422E mice.Echevarria-Cooper D.M., Hawkins N.A., Misra S.N., Huffman A.M., Thaxton T., Thompson C.H., Ben-Shalom R., Nelson A.D., Lipkin A.M.[...], Kearney J.A.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 98248PubMedEurope PMCHum Mol Genet 31:2964-2988 (2022)Mapped to13
Deficiency of autism-related Scn2a gene in mice disrupts sleep patterns and circadian rhythms.Ma Z., Eaton M., Liu Y., Zhang J., Chen X., Tu X., Shi Y., Que Z., Wettschurack K.[...], Yang Y.View abstractAnnotationDeficiency of autism-related Scn2a gene in mice disrupts sleep patterns and circadian rhythms.CategoryPhenotypes & VariantsSourceGeneRif: 110876, MGI: 98248PubMedEurope PMCNeurobiol Dis 168:105690-105690 (2022)Mapped to13
Sodium channel expression and transcript variation in the developing brain of human, Rhesus monkey, and mouse.Heighway J., Sedo A., Garg A., Eldershaw L., Perreau V., Berecki G., Reid C.A., Petrou S., Maljevic S.View abstractCategoriesSequences, ExpressionSourceMGI: 98248PubMedEurope PMCNeurobiol Dis 164:105622-105622 (2022)Mapped to41