1. Genes and Genomic Entities
  2. SLCO2A1

SLCO2A1

solute carrier organic anion transporter family member 2A1
OMIM: 601460, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Green SLCO2A1 in Primary immunodeficiency or monogenic inflammatory bowel disease


Version 5.3
Latest signed off version: v5.0 (1 May 2024)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
Phenotypes
  • Prostaglandin transporter deficiency
Green SLCO2A1 in Autosomal recessive primary hypertrophic osteoarthropathy


Version 1.12
Latest signed off version: v1.5 (11 Nov 2020)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • London North GLH
  • NHS GMS
  • Expert Review Green
Phenotypes
  • Hypertrophic osteoarthropathy, primary, autosomal recessive 2 OMIM:614441
Green SLCO2A1 in Skeletal dysplasia

Level 3: Skeletal dysplasias
Level 2: Skeletal disorders
Version 5.3
Latest signed off version: v5.0 (1 May 2024)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Green
    Phenotypes
    • Hypertrophic osteoarthropathy, primary, autosomal recessive 2 614441
    • Hypertrophic osteoarthropathy, primary, autosomal recessive 2 614441
    Green SLCO2A1 in Severe Paediatric Disorders


    Version 1.184

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Next Generation Children Project
    • Expert Review Green
    • Expert list
    Phenotypes
    • Hypertrophic osteoarthropathy, primary, autosomal recessive 2, 614441