例如:"NBL1", "4681", "drought"
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54014 BRWD1

54014

BRWD1

bromodomain and WD repeat domain containing 1

protein-coding

Homo sapiens

基因描述

Type Description
Definition bromodomain and WD repeat domain containing 1

研究结论

Date Results Publications
2019-01-19 11:16:00 Study data indicate that, in both mice and humans, BRWD1 is a master orchestrator of enhancer accessibility that cooperates with transcription factor networks to drive late B-cell development. 30250168
2016-05-09 12:02:00 RNA-seq evidence of biallelic expression of BRWD1 and 10 neighboring genes in at least one primary human tissue tested indicates that the expression of BRWD1 is uncoupled from the control of the maternally inherited 5mCpG imprints at the WRB differentially methylated region (DMR) in disomic controls or trisomy (Down syndrome) individuals. 27100087
2010-06-30 22:05:00 Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) 20379614
2010-04-07 21:40:00 Observational study and genome-wide association study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) 20014019
2010-01-21 00:00:00 isolation and characterization of the gene located in the Down Syndrome critical region-2 of chromosome 21 12359327

名称对应

Type IDs
Synonymous C21orf107, DCAF19, N143, WDR9, WRD9
Gene
UniProtKB-ID: BRWD1_HUMAN
UniprotKB: Q9NSI6
UniParc: UPI0000163C12, UPI0000231C57, UPI00004DE96F, UPI0000163C13
EMBL: AL163279, AK002177, AJ292466, AF064861, AJ292465, AJ222636, AB080586, AB080587, BC064602, AJ238214, AF129408
Ensembl: ENSG00000185658
KO: hsa:54014
Nucleutide sequences
EMBL-CDS: BAD74072.1, CAC44371.1, AAH64602.1, BAD74071.1, CAC37033.2, CAB90452.1, CAC44372.1, CAA10896.1
Ensembl_TRS: ENST00000342449, ENST00000380800, ENST00000333229, ENST00000341322
Protein sequencees
Ensembl_PRO: ENSP00000330753, ENSP00000344333, ENSP00000342106, ENSP00000370178
RefSeq: NP_001007247.1, NP_061836.2, NP_387505.1, XP_011527914.1, XP_016883863.1, XP_011527915.1, XP_011527913.1, XP_016883862.1, XP_016883864.1
Others
UniRef100: UniRef100_Q9NSI6
UniRef90: UniRef90_Q9NSI6
UniRef50: UniRef50_Q9NSI6
UniGene: Hs.627139, Hs.654740
CCDS: CCDS13662.1, CCDS13663.1, CCDS33557.1

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