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Gene : CHD2 Homo sapiens

Name  ? chromodomain helicase DNA binding protein 2 Cytological Location  15q26.1
Brief Description  chromodomain helicase DNA binding protein 2
Description  The CHD family of proteins is characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains. CHD genes alter gene expression possibly by modification of chromatin structure thus altering access of the transcriptional apparatus to its chromosomal DNA template. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
  • synonyms:
  • OTTHUMG00000185958,
  • DKFZp781D1727,
  • AF006514,
  • CHD2,
  • DKFZp547I1315,
  • HGNC:1917,
  • DKFZp686E01200,
  • FLJ38614,
  • EEOC,
  • NM_001271,
  • uc002bsp.4
  • identifiers:
  • 1106,
  • ENSG00000173575,
  • CHD2

Genome feature

Region: gene ? Length: 127673  
Location: 15:92900324-93027996 Cyto location: 15q26.1

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Gene Expression Atlas Diseases Displayer

Publication Counts Displayer

Curated Proteins Displayer


Gene Ontology Displayer

0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


Homologue Displayer


Cytoscape Network Displayer

Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



0 Pathways

89 SN Ps

5 Cross References

18 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results