SLCO2A1

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

4 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Green SLCO2A1 in Primary immunodeficiency or monogenic inflammatory bowel disease Level 2: Immunology Version 8.78 Latest signed off version: v8.0 (30 Apr 2025)	review	BIALLELIC, autosomal or pseudoautosomal	Sources 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 Tags Q2_25_ MOI
Green SLCO2A1 in Autosomal recessive primary hypertrophic osteoarthropathy Level 2: Dermatology Version 1.17 Latest signed off version: v1.5 (11 Nov 2020)	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 8.34 Latest signed off version: v8.0 (30 Apr 2025) 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 OMIM:614441 hypertrophic osteoarthropathy, primary, autosomal recessive, 2, MONDO:0013756 Hypertrophic osteoarthropathy, primary, autosomal dominant, OMIM:167100 hypertrophic osteoarthropathy, primary, autosomal dominant, MONDO:0008172 Tags Q2_25_ MOI
Red SLCO2A1 in Fetal anomalies Level 2: Fetal (including NIPD) Version 6.140 Latest signed off version: v6.0 (30 Apr 2025)	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