CHD3 wt Allele

Preferred Label : CHD3 wt Allele;

NCIt synonyms : SNIBCPS; Chromodomain Helicase DNA Binding Protein 3 wt Allele; ZFH; Mi-2a; Mi2-ALPHA; Zinc-Finger Helicase (Snf2-Like) Gene;

NCIt definition : Human CHD3 wild-type allele is located in the vicinity of 17p13.1 and is approximately 28 kb in length. This allele, which encodes chromodomain-helicase-DNA-binding protein 3, plays a role in mitosis, transcriptional repression and chromatin remodeling. Mutation of the gene is associated with Snijders Blok-Campeau syndrome.;

GenBank Accession Number : U08379;

Details

Origin ID

C200608;

OMIM relation
- Chromodomain helicase dna-binding protein 3 [OMIM gene]
See also inter- (CISMeF)
- Snijders Blok-Campeau syndrome [MeSH Supplementary Concept]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 17p13.1 [NCIt concept]
gene_plays_role_in_process
- ATP Hydrolysis [NCIt concept]
- Chromatin Remodeling [NCIt concept]
- DNA Binding [NCIt concept]
- Hydrolysis [NCIt concept]
- Transcriptional Regulation [NCIt concept]

Keyword's position in hierarchy(ies) :

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