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Gene : CHD7 Homo sapiens

Name  ? chromodomain helicase DNA binding protein 7 Cytological Location  8q12.2
Brief Description  chromodomain helicase DNA binding protein 7
Description  This gene encodes a protein that contains several helicase family domains. Mutations in this gene have been found in some patients with the CHARGE syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]
  • synonyms:
  • KIAA1416,
  • FLJ20357,
  • CRG,
  • HGNC:20626,
  • AB037837,
  • uc003xue.4,
  • CHARGE association,
  • CHD7,
  • HH5,
  • CRG,
  • FLJ20361,
  • KAL5,
  • IS3,
  • OTTHUMG00000165332,
  • NM_017780
  • identifiers:
  • 55636,
  • ENSG00000171316,
  • CHD7

Genome feature

Region: gene ? Length: 189289  
Location: 8:60678740-60868028 Cyto location: 8q12.2


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Function

Gene Ontology Displayer

0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

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

2 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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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

558 SN Ps

5 Cross References

18 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results