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


Level 2: Immunology
Version 9.9
Latest signed off version: v9.0 (6 May 2026)

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Green
Phenotypes
  • Hypertrophic osteoarthropathy, primary, autosomal recessive 2 OMIM:614441
  • hypertrophic osteoarthropathy, primary, autosomal recessive, 2, MONDO:0013756
  • Hypertrophic osteoarthropathy, primary, autosomal dominant, OMIM:167100
  • hypertrophic osteoarthropathy, primary, autosomal dominant, MONDO:0008172
Green SLCO2A1 in Autosomal recessive primary hypertrophic osteoarthropathy


Level 2: Dermatology
Version 2.1
Latest signed off version: v2.0 (6 May 2026)

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • London North GLH
  • NHS GMS
  • Expert Review Green
Phenotypes
  • Hypertrophic osteoarthropathy, primary, autosomal recessive 2 OMIM:614441
  • hypertrophic osteoarthropathy, primary, autosomal recessive, 2, MONDO:0013756
  • Hypertrophic osteoarthropathy, primary, autosomal dominant, OMIM:167100
  • hypertrophic osteoarthropathy, primary, autosomal dominant, MONDO:0008172
Green SLCO2A1 in Skeletal dysplasia


Level 2: Musculoskeletal
Version 9.9
Latest signed off version: v9.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Green
    Phenotypes
    • Hypertrophic osteoarthropathy, primary, autosomal recessive 2 OMIM:614441
    • hypertrophic osteoarthropathy, primary, autosomal recessive, 2, MONDO:0013756
    • Hypertrophic osteoarthropathy, primary, autosomal dominant, OMIM:167100
    • hypertrophic osteoarthropathy, primary, autosomal dominant, MONDO:0008172
    Red SLCO2A1 in Fetal anomalies


    Level 2: Fetal (including NIPD)
    Version 7.7
    Latest signed off version: v7.0 (6 May 2026)

    		review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • NHS GMS
    Phenotypes
    • Hypertrophic osteoarthropathy, primary, autosomal dominant, OMIM:167100
    • PHOAR2-enteropathy syndrome, OMIM:614441