ASH1L wt Allele

**Semantic type:** Gene or Genome

**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.

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