protein-coding gene of Mus musculus Atrx 10090 20140409 22589 4833408C14Rik AI447451 ATR2 Atrx Bin Zhao, Yue Liu, Oliver He DXHXS6677E Ensembl:ENSMUSG00000031229 GO_0000166 (EC: IEA); GO_0000228 (EC: IDA, PMID: 11555636); GO_0000792 (EC: IDA, PMID: 14519686); GO_0003676 (EC: IEA); GO_0003677 (EC: IEA); GO_0003682 (EC: IDA, PMID: 15522233); GO_0004386 (EC: IEA); GO_0005515 (EC: IPI, PMID: 8978696); GO_0005524 (EC: IEA); GO_0005634 (EC: IDA, PMID: 17296936); GO_0005634 (EC: ISO); GO_0005730 (EC: ISO); GO_0005737 (EC: ISO); GO_0005739 (EC: ISO); GO_0006281 (EC: IEA); GO_0006974 (EC: IEA); GO_0007283 (EC: IMP); GO_0008270 (EC: IEA); GO_0016787 (EC: IEA); GO_0030900 (EC: IMP, PMID: 15668733); GO_0045944 (EC: IGI); GO_0046872 (EC: IEA); GO_0060009 (EC: IMP); GO_0070087 (EC: ISO); GO_0072520 (EC: IMP) HP1-BP38 Hp1bp2 Hp1bp38 MGI:103067 MRXS3 Official from a nomenclature committee Other designations: ATP-dependent helicase ATRX|HP1 alpha-interacting protein|X-linked nuclear protein|alpha thalassemia/mental retardation syndrome (X-linked)|heterochromatin protein 2|transcriptional regulator ATRX PMID: 7874112; 8162050; 8889548; 8921375; 8978696; 9545503; 9607915; 9736627; 10349636; 10570185; 10757799; 10922068; 11042159; 11076861; 11217851; 11544199; 11555636; 11823444; 12466851; 12520002; 12904583; 14519686; 14610273; 14681479; 15242786; 15252119; 15522233; 15668733; 16141072; 16141073; 16452087; 16602821; 16628246; 16935872; 17296936; 17503331; 18227278; 18287559; 18366812; 18799693; 18842153; 19005673; 19020049; 19088125; 19538749; 19571810; 19615340; 19774083; 20110566; 20150414; 20159591; 20211137; 20548051; 20651253; 20865721; 20885787; 21029860; 21057507; 21209221; 21267068; 21317870; 21357745; 21421568; 21427128; 21672208; 21677750; 22500635; 22573614; 22918800; 23114596; 23284920; 23362347; 23563309; 23892236 RAD54L RP23-170G19.5 Rad54 Vega:OTTMUSG00000018268 WEB: http://www.ncbi.nlm.nih.gov/gene X X D|X 47.26 cM XH2 Xnp ZNF-HX alpha thalassemia/mental retardation syndrome X-linked homolog (human) alpha thalassemia/mental retardation syndrome X-linked homolog (human) protein-coding