CHD2 wt Allele

Preferred Label : CHD2 wt Allele;

NCIt synonyms : DKFZp547I1315; Chromodomain Helicase DNA Binding Protein 2 wt Allele; DKFZp781D1727; FLJ38614; DKFZp686E01200;

NCIt definition : Human CHD2 wild-type allele is located in the vicinity of 15q26 and is approximately 125 kb in length. This allele, which encodes chromodomain-helicase-DNA-binding protein 2, may play a role in the modulation of both chromatin structure and gene expression. Deletion of this gene may be associated with congenital diaphragmatic hernia.;

GenBank Accession Number : AF006514;

Details

Origin ID

C75308;

UMLS CUI

C2698724;

Automatic exact mappings (from CISMeF team)
- chromodomain helicase DNA binding protein 2 [ORDO Gene]
OMIM relation
- Chromodomain helicase dna-binding protein 2 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 15q26 [NCIt concept]
gene_plays_role_in_process
- ATP Hydrolysis [NCIt concept]
- Chromatin Remodeling [NCIt concept]
- DNA Binding [NCIt concept]
- DNA Topology Regulation [NCIt concept]
- Hydrolysis [NCIt concept]

Keyword's position in hierarchy(ies) :

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