BRWD3

GENE INFORMATION

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Gene name

BRWD3 (HGNC Symbol)

Synonyms

FLJ38568, MRX93

Description

bromodomain and WD repeat domain containing 3 (HGNC Symbol)

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]

Chromosome

X (Chromosome progress)

Cytoband

q21.1

Chromosome location (bp)

79926353 - 80065187

Ensembl

ENSG00000165288 (version 73.37)

Entrez gene

254065

UniProt

Q6RI45 (UniProt - Evidence at protein level)

neXtProt

NX_Q6RI45

Antibodypedia

BRWD3 antibodies
 

PROTEIN VIEW

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BRWD3-001
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

BRWD3-001 ENSP00000362372
ENST00000373275
Q6RI45
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