CECR2

GENE INFORMATION

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Gene name

CECR2 (HGNC Symbol)

Synonyms

KIAA1740

Description

Cat eye syndrome chromosome region, candidate 2 (HGNC Symbol)

Entrez gene summary

This gene encodes a bromodomain-containing protein that is involved in chromatin remodeling, and may additionally play a role in DNA damage response. The encoded protein functions as part of an ATP-dependent complex that is involved in neurulation. This gene is a candidate gene for Cat Eye Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]

Chromosome

22

Cytoband

q11.1

Chromosome location (bp)

17840837 - 18037850

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000099954 (version 75.37)

Entrez gene

27443

UniProt

Q9BXF3 (UniProt - Evidence at protein level)

neXtProt

NX_Q9BXF3

Antibodypedia

CECR2 antibodies
 

PROTEIN VIEW

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CECR2-001
 
CECR2-002
 
CECR2-004
 
CECR2-201
 
CECR2-202
 
 
 
 
 

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)

CECR2-001 ENSP00000383417
ENST00000400573
E2QRE6
Show all »
Show » Show » 1442 159.7 No 0
CECR2-002 ENSP00000383428
ENST00000400585
B7WPH3
Show all »
Show » Show » 1300 143.1 No 0
CECR2-004 ENSP00000347357
ENST00000355219
H0Y2Z1
Show all »
Show » 218 23.8 No 0
CECR2-201 ENSP00000262608
ENST00000262608
Q9BXF3
Show all »
Show » Show » 1443 159.6 No 0
CECR2-202 ENSP00000341219
ENST00000342247
H7BXW8
Show all »
Show » Show » 456 53.4 No 0