HNRNPH2 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human HNRNPH2 wild-type allele is located in the vicinity of Xq22.1 and is approximately 6 kb in length. This allele, which encodes heterogeneous nuclear ribonucleoprotein H2, plays a role in the maturation of messenger RNA. Mutation of the gene is associated with the Bain type of X-linked syndromic mental retardation and may be associated with Fabray disease and X-linked agammaglobulinemia.

**Synonyms:** - FTP3 - HNRPH' - HNRPH2 - Heterogeneous Nuclear Ribonucleoprotein H' Gene - Heterogeneous Nuclear Ribonucleoprotein H-Prime Gene - Heterogeneous Nuclear Ribonucleoprotein H2 (H') Gene - Heterogeneous Nuclear Ribonucleoprotein H2 wt Allele - MRXSB - NRPH2 - hnRNPH'