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Gene : CHD1 Homo sapiens

Name  ? chromodomain helicase DNA binding protein 1 Cytological Location  5q15-q21.1
Brief Description  chromodomain helicase DNA binding protein 1
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. [provided by RefSeq, Jul 2008]
  • synonyms:
  • AF006513,
  • CHD1,
  • uc063frt.1,
  • CHD-1,
  • NM_001270,
  • HGNC:1915,
  • OTTHUMG00000162744
  • identifiers:
  • 1105,
  • ENSG00000153922,
  • CHD1

Genome feature

Region: gene ? Length: 75788  
Location: 5:98853985-98929772 reverse strand Cyto location: 5q15-q21.1

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

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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]


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Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



103 SN Ps

5 Cross References

19 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results