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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:
  • CHD2,
  • uc002bsp.4,
  • DKFZp547I1315,
  • EEOC,
  • DKFZp686E01200,
  • NM_001271,
  • DKFZp781D1727,
  • HGNC:1917,
  • AF006514,
  • OTTHUMG00000185958,
  • FLJ38614
  • identifiers:
  • 1106,
  • ENSG00000173575,
  • CHD2

Genome feature

Region: gene ? Length: 127687  
Location: 15:92900321-93028007 Cyto location: 15q26.1


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Function

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0 Pathways

Gene --> GO terms.

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

1 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Mouse Gene --> Allele [Phenotype]

Homology

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Gene --> Orthologues

Interactions

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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

25 SN Ps

5 Cross References

18 Data Sets

13 Homologues

0 Located Features

90 Rna Seq Results