prostaglandin transporter, partial [Homo sapiens]

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Genotype and phenotype characterization of primary hypertrophic osteoarthropathy type 2 and chronic enteropathy associated with SLCO2A1: Report of two cases and literature review. [Am J Med Genet A. 2024]
Genotype and phenotype characterization of primary hypertrophic osteoarthropathy type 2 and chronic enteropathy associated with SLCO2A1: Report of two cases and literature review.
Kimball TN, Rivero-García P, Barrera-Godínez A, Domínguez-Cherit J. Am J Med Genet A. 2024 Mar; 194(3):e63446. Epub 2023 Nov 1.
Identification of three novel mutations in SLCO2A1 in Asian-Indians with Pachydermoperiostosis. [Indian J Med Res. 2023]
Identification of three novel mutations in SLCO2A1 in Asian-Indians with Pachydermoperiostosis.
Pasumarthi D, Ranganath P, Mandal K, Lakshmi ND, Dalal A, Aggarwal S. Indian J Med Res. 2023 Sep; 158(3):319-323.
Attenuated Expression of SLCO2A1 Caused by DNA Methylation in Pediatric Inflammatory Bowel Disease. [Inflamm Bowel Dis. 2023]
Attenuated Expression of SLCO2A1 Caused by DNA Methylation in Pediatric Inflammatory Bowel Disease.
Ito N, Kudo T, Eguchi H, Jimbo K, Furuhata A, Okuno T, Takeuchi I, Arai K, Ishige T, Okazaki Y, et al. Inflamm Bowel Dis. 2023 Dec 5; 29(12):1920-1928.

RefSeq genomic sequence
See the genomic reference sequence for the SLCO2A1 gene (NG_031964.3).
RefSeq protein
See the reference protein sequence for solute carrier organic anion transporter family member 2A1 (NP_005621.2).

Nucleotide
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prostaglandin transporter, partial [Homo sapiens]
prostaglandin transporter, partial [Homo sapiens]
gi|68445515|dbj|BAE03225.1|

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Protein