BRWD1

GENERAL INFORMATION

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Gene name

BRWD1

Gene description

Bromodomain and WD repeat domain containing 1

Protein class

Plasma proteins
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

6
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Ubiquitous cytoplasmic and membranous expression.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 4 antibodies.
HPA030943 , HPA030944 , HPA030945 , CAB034184
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Gallbladder

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

BRWD1 (HGNC Symbol)

Synonyms

C21orf107, FLJ11315, N143, WDR9

Description

Bromodomain and WD repeat domain containing 1 (HGNC Symbol)

Entrez gene summary

This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD) residues which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein contains 2 bromodomains and multiple WD repeats. This gene is located within the Down syndrome region-2 on chromosome 21. Alternative splicing of this gene generates multiple transcript variants encoding distinct isoforms. In mouse, this gene encodes a nuclear protein that has a polyglutamine-containing region that functions as a transcriptional activation domain which may regulate chromatin remodelling and associates with a component of the SWI/SNF chromatin remodelling complex.[provided by RefSeq, Jun 2011]

Chromosome

21

Cytoband

q22.2

Chromosome location (bp)

39184176 - 39321559

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000185658 (version 78.38)

Entrez gene

54014

UniProt

Q9NSI6 (UniProt - Evidence at protein level)

neXtProt

NX_Q9NSI6

Antibodypedia

BRWD1 antibodies


PROTEIN BROWSER

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ENST00000333229
 
ENST00000341322
 
ENST00000342449
 
ENST00000380800
 
ENST00000424441
 
ENST00000455867
 
 
 
 


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)

BRWD1-001 ENSP00000330753
ENST00000333229
Q9NSI6
Show all »
Show » Show » 2320 262.9 No 0
BRWD1-002 ENSP00000344333
ENST00000342449
Q9NSI6
Show all »
Show » Show » 2269 257.2 No 0
BRWD1-004 ENSP00000342106
ENST00000341322
Q9NSI6
Show all »
Show » Show » 120 13.6 No 0
BRWD1-010 ENSP00000415066
ENST00000424441
Show » Show » 452 51.9 No 0
BRWD1-014 ENSP00000389882
ENST00000455867
Q5R2U6
Show all »
Show » Show » 548 62.2 No 0
BRWD1-016 ENSP00000370178
ENST00000380800
Q9NSI6
Show all »
Show » Show » 2199 249 No 0