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GENE INFORMATION

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Gene name

WDR4 (HGNC Symbol)

Synonyms

TRM82, TRMT82

Description

WD repeat domain 4 (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), 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 gene is excluded as a candidate for a form of nonsyndromic deafness (DFNB10), but is still a candidate for other disorders mapped to 21q22.3 as well as for the development of Down syndrome phenotypes. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2012]

Chromosome

21 (Chromosome progress)

Cytoband

q22.3

Chromosome location (bp)

44263204 - 44299678

Ensembl

ENSG00000160193 (version 69.37)

Entrez gene

10785

UniProt

P57081

neXtProt

NX_P57081

Antibodypedia

WDR4 antibodies
 

PROTEIN VIEW

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WDR4-001
 
WDR4-004
 
 
 
 
 

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)

WDR4-001 ENSP00000381266
ENST00000398208
P57081
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Show » Show » 412 45.5 No 0
WDR4-004 ENSP00000328671
ENST00000330317
P57081
Show all »
Show » Show » 412 45.5 No 0