METTL13 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human METTL13 wild-type allele is located in the vicinity of 1q24.3 and is approximately 32 kb in length. This allele, which encodes eEF1A lysine and N-terminal methyltransferase protein, plays a role in the modulation of both apoptosis and protein translation. Mutation of the gene is associated with type 26 autosomal recessive deafness.

**Synonyms:** - 5630401D24Rik - CGI-01 - DFNB26 - DFNB26M - DFNM1 - Deafness (Autosomal Recessive, Nonsyndromic) Modifier 1 Gene - Deafness (Recessive, Non-Syndromic) Modifier 1 Gene - Deafness (Recessive, Nonsyndromic) Modifier 1 Gene - Deafness, Autosomal Recessive 26 Gene - FEAT - Faint Expression in Normal Tissues, Aberrant Overexpression in Tumors Gene - KIAA0859 - METTL13 - Methyltransferase 13, eEF1A Lysine and N-Terminal Methyltransferase Gene - Methyltransferase 13, eEF1A N-Terminus and K55 wt Allele - Methyltransferase Like 13 Gene - Methyltransferase-Like 13 Gene - eEF1A Lysine and N-Terminal Methyltransferase Gene - feat