SLCO2A1 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human SLCO2A1 wild-type allele is located within 3q22.1-q22.2 and is approximately 119 kb in length. This allele, which encodes solute carrier organic anion transporter family member 2A1 protein, is involved in eicosanoid transport. Mutations in the gene are associated with primary autosomal dominant hypertrophic osteoarthropathy and primary autosomal dominant hypertrophic osteoarthropathy 2 (PHOAR2-enteropathy syndrome).

**Synonyms:** - MATR1 - Matrin F/G 1 Gene - OATP2A1 - Organic Anion Transporter 2A1 Gene - PGT - PHOAD - PHOAR2 - SLC21A2 - Solute Carrier Family 21 (Prostaglandin Transporter), Member 2 Gene - Solute Carrier Organic Anion Transporter Family Member 2A1 wt Allele - Solute Carrier Organic Anion Transporter Family, Member 2A1 Gene