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42898 BRWD3

42898

BRWD3

BRWD3

protein-coding

Drosophila melanogaster

基因描述

Type Description
Definition BRWD3

研究结论

Date Results Publications
2020-05-09 12:05:00 study delineates the clinical features associated with BRWD3 null variants and partial gene deletions, and suggests that BRWD3 should be included in the differential diagnosis of patients with an overgrowth-intellectual disability (OGID) phenotype, particularly in male patients with a mild or moderate intellectual disability associated with macrocephaly and/or obesity 31714006
2017-05-27 10:20:00 Our findings identified dBRWD3 as a critical regulator that is uniquely required for ectopic gene expression and aberrant tissue overgrowth caused by PcG mutations. 27588417
2015-12-26 10:16:00 Intellectual disability-associated BRWD3 regulates gene expression through inhibition of HIRA/YEM-mediated chromatin deposition of histone H3.3. 25666827
2013-05-25 11:04:00 BRWD3 functions as a Damage-specific DNA binding protein 1 (DDB1)- and CULLIN (CUL)4-associated factor in a Cullin4-RING Finger E3 Ligase (CRL4) that mediates light-dependent binding of dCRY to CUL4-ROC1-DDB1-BRWD3, inducing ubiquitylation of dCRY 23479607
2010-01-21 00:00:00 In the developing retina, ramshackle (ram) mutant cells have morphological defects including disrupted apical junctions, disorganized actin cytoskeletons and mislocalized nuclei. 16904300

名称对应

Type IDs
Synonymous Brwd3, CG18670, CG31132, CG6400, Dmel\CG31132, anon-WO0118547.520, anon-WO0118547.620, brwd3, dBRWD3, l(3)05842, l(3)s5349, psg13, ram
Gene
UniProtKB-ID: Q9VC96_DROME
UniprotKB: Q9VC96
UniParc: UPI0000083039
EMBL: AE014297
EnsemblGenome: FBgn0011785
KO: dme:Dmel_CG31132
Nucleutide sequences
EMBL-CDS: AAF56278.2
Gene_ORFName: Dmel_CG31132, CG31132
EnsemblGenome_TRS: FBtr0084604
Protein sequencees
EnsemblGenome_PRO: FBpp0083988
RefSeq: NP_732982.1
Others
UniRef100: UniRef100_Q9VC96
UniRef90: UniRef90_Q9VC96
UniRef50: UniRef50_Q9VC96
UniGene: Dm.5099

全选

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