ASH1L wt Allele

Preferred Label : ASH1L wt Allele;

NCIt synonyms : ASH1-Like Gene; ASH1, Drosophila, Homolog of Gene; ASH1; MRD52; KIAA1420; ASH1L1; ASH1 Like Histone Lysine Methyltransferase wt Allele; Probable Histone-Lysine N-Methyltransferase ASH1L Gene; KMT2H; Ash1 (Absent, Small, or Homeotic)-Like (Drosophila) Gene; Ash1 (Absent, Small, or Homeotic)-Like Gene;

NCIt definition : Human ASH1L wild-type allele is located in the vicinity of 1q22 and is approximately 228 kb in length. This allele, which encodes histone-lysine N-methyltransferase ASH1L protein, plays a role in histone-lysine methylation and chromatin remodeling. Mutations of the gene are associated with autosomal dominant intellectual developmental disorder 52.;

GenBank Accession Number : AB037841;

Détails

Origin ID

C215310;

OMIM relation
- Ash1-like histone lysine methyltransferase [OMIM gene]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 1q22 [NCIt concept]
gene_is_element_in_pathway
- Lysine Degradation Pathway [NCIt concept]
gene_plays_role_in_process
- Chromatin Remodeling [NCIt concept]
- Gene Expression [NCIt concept]
- Histone Methylation [NCIt concept]
- Methylation [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients