Homo sapiens Gene: BRWD3
Summary
InnateDB Gene IDBG-78204.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol BRWD3
Gene Name bromodomain and WD repeat domain containing 3
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000165288
Encoded Proteins
bromodomain and WD repeat domain containing 3
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The protein encoded by this gene contains a bromodomain and several WD repeats. It is thought to have a chromatin-modifying function, and may thus play a role in transcription. Mutations in this gene cause mental retardation X-linked type 93, which is also referred to as mental retardation X-linked with macrocephaly. This gene is also associated with translocations in patients with B-cell chronic lymphocytic leukemia. [provided by RefSeq, May 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome X:80670854-80809688
Strand Reverse strand
Band q21.1
Transcripts
ENST00000373275 ENSP00000362372
ENST00000473691
ENST00000497335
ENST00000487313
ENST00000478415
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
GO:0007010 cytoskeleton organization
GO:0008360 regulation of cell shape
Cellular Component
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.147027 Hs.600970
RefSeq NM_153252 XM_005262115 XM_006724638
HUGO
OMIM
CCDS CCDS14447
HPRD 06564
IMGT
EMBL
GenPept
RNA Seq Atlas