HNRNPA1 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human HNRNPA1 wild-type allele is located in the vicinity of 12q13.13 and is approximately 7 kb in length. This allele, which encodes heterogeneous nuclear ribonucleoprotein A1, is involved in RNA transport and splicing. Mutation of the gene is associated with inclusion body myopathy with early-onset Paget disease without frontotemporal dementia 3 and amyotrophic lateral sclerosis 20.

**Synonyms:** - ALS19 - ALS20 - HNRPA1 - HNRPA1L3 - Heterogeneous Nuclear Ribonucleoprotein A1 wt Allele - HnRNP Core Protein A1-Like 3 Gene - IBMPFD3 - Putative Heterogeneous Nuclear Ribonucleoprotein A1-Like 3 Gene - UP 1 - hnRNP A1 - hnRNP-A1