Hr - HR, lysine demethylase and nuclear receptor corepressor-BMKCloudï½ç¾è¿å®¢äº

例如："NBL1", "4681", "drought"

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60563 Hr

基因描述

Type	Description
Definition	HR, lysine demethylase and nuclear receptor corepressor

研究结论

Date	Results	Publications
2010-08-23 11:58:00	Hr and VDR interact via multiple protein-protein interfaces, catalyzing histone demethylation to effect chromatin remodeling and repress the transcription of VDR target genes that control the hair cycle.	20512927
2010-01-21 00:00:00	histopathologic changes in heterozygous and homozygous CR hairless rat mutants during the first month of life	11926302

名称对应

Type	IDs
Gene	UniProtKB-ID: A0A0G2K5M5_RAT UniprotKB: A0A0G2K5M5 UniParc: UPI000154D51C EMBL: CH473951, AABR07018330 Ensembl: ENSRNOG00000011427 KO: rno:60563
Nucleutide sequences	EMBL-CDS: EDM02229.1, EDM02227.1, EDM02228.1 Gene_ORFName: rCG_36905 Ensembl_TRS: ENSRNOT00000082639
Protein sequencees	Ensembl_PRO: ENSRNOP00000073482 RefSeq: NP_077340.3, XP_006252345.2
Others	UniRef100: UniRef100_G3V7J4 UniRef90: UniRef90_Q61645 UniRef50: UniRef50_O43593 UniGene: Rn.41543

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mRNA

Protein

UniprotKB

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Pubmed编号	文献信息	发表日期	相关基因
21873635	Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Brief. Bioinformatics Pascale Gaudet , Michael S Livstone , Suzanna E Lewis , Paul D Thomas	2011-09-01	-
20512927	Analysis of hairless corepressor mutants to characterize molecular cooperation with the vitamin D receptor in promoting the mammalian hair cycle. J. Cell. Biochem. Jui-Cheng Hsieh , Stephanie A Slater , G Kerr Whitfield , Jamie L Dawson , Grace Hsieh , Craig Sheedy , Carol A Haussler , Mark R Haussler	2010-06-01	Vdr, Hr, HR, VDR
19122663	Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis. Nat. Genet. Yaran Wen , Yang Liu , Yiming Xu , Yiwei Zhao , Rui Hua , Kaibo Wang , Miao Sun , Yuanhong Li , Sen Yang , Xue-Jun Zhang , Roland Kruse , Sven Cichon , Regina C Betz , Markus M NÃ¶then , Maurice A M van Steensel , Michel van Geel , Peter M Steijlen , Daniel Hohl , Marcel Huber , Giles S Dunnill , Cameron Kennedy , Andrew Messenger , Colin S Munro , Alessandro Terrinoni , Alain Hovnanian , Christine Bodemer , Yves de Prost , Amy S Paller , Alan D Irvine , Rod Sinclair , Jack Green , Dandan Shang , Qing Liu , Yang Luo , Li Jiang , Hong-Duo Chen , Wilson H-Y Lo , W H Irwin McLean , Chun-Di He , Xue Zhang	2009-02-01	Hr, Hr, HR, FAM160B2, FGF17
12847098	Physical and functional interaction between the vitamin D receptor and hairless corepressor, two proteins required for hair cycling. J Biol Chem Jui-Cheng Hsieh , Jeanne M Sisk , Peter W Jurutka , Carol A Haussler , Stephanie A Slater , Mark R Haussler , Catherine C Thompson	2003-10-03	-
12873232	Linkage mapping of the porcine hairless gene (HR ) to chromosome 14. Anim. Genet. A FernÃ¡ndez , L SiliÃ³ , J L Noguera , A SÃ¡nchez , C Ovilo	2003-08-01	-
12403844	The thyroid hormone-regulated corepressor hairless associates with histone deacetylases in neonatal rat brain. Mol. Endocrinol. Gregory B Potter , Joanna M Zarach , Jeanne M Sisk , Catherine C Thompson	2002-11-01	Hr, Hdac1, Hr, Hdac2, Hdac3, HDAC2, HR, HDAC3
11641275	The hairless gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor. Genes Dev. G B Potter , G M Beaudoin , C L DeRenzo , J M Zarach , S H Chen , C C Thompson	2001-10-15	Hdac3, Hdac5, Hr, Rara, Srsf2, Ncor2, Thra, Hdac1, Hr, HDAC5, HDAC1, HDAC2, HR, THRA, HDAC3
11926302	The Charles River "hairless" rat mutation is distinct from the hairless mouse alleles. Comp. Med. A A Panteleyev , A M Christiano	2001-02-01	Hr, Hr
9736769	Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia. Hum. Mol. Genet. S Cichon , M Anker , I R Vogt , H Rohleder , M PÃ¼tzstÃ¼ck , A Hillmer , S A Farooq , K S Al-Dhafri , M Ahmad , S Haque , M Rietschel , P Propping , R Kruse , M M NÃ¶then	1998-10-01	-
9856480	Congenital atrichia in five Arab Palestinian families resulting from a deletion mutation in the human hairless gene. Hum. Genet. A Zlotogorski , W Ahmad , A M Christiano	1998-10-01	-

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