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Gene : CECR2 Homo sapiens

Name  ? CECR2 histone acetyl-lysine reader Cytological Location  22q11.1-q11.21
Brief Description  CECR2 histone acetyl-lysine reader
Description  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]
  • synonyms:
  • AF336133,
  • OTTHUMG00000150072,
  • cat eye syndrome chromosome region, candidate 2,
  • CECR2,
  • KIAA1740,
  • HGNC:1840,
  • uc010gqv.2,
  • NM_031413
  • identifiers:
  • 27443,
  • ENSG00000099954,
  • CECR2

Genome feature

Region: gene ? Length: 198203  
Location: 22:17359949-17558151 Cyto location: 22q11.1-q11.21

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

389 SNPs

5 Cross References

16 Data Sets

2 Homologues

0 Located Features

97 Rna Seq Results