SLCO2A1

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

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green SLCO2A1 in Inflammatory bowel disease Level 2: Gastroenterological disorders Version 0.121 Component of the following Super Panels: Immunological disorders_SuperPanel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Inflammatory bowel disease, MONDO:0005265, SLCO2A1-related Enteropathy
Green SLCO2A1 in Mendeliome Version 1.1891	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Hypertrophic osteoarthropathy, primary, autosomal dominant, MIM# 167100 Hypertrophic osteoarthropathy, primary, autosomal recessive 2, MIM# 614441 Inflammatory bowel disease, MONDO:0005265, SLCO2A1-related
Green SLCO2A1 in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.285	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green NHS GMS Phenotypes Hypertrophic osteoarthropathy, primary, autosomal recessive 2 614441 Hypertrophic osteoarthropathy, primary, autosomal recessive 2 614441
Green SLCO2A1 in Additional findings_Paediatric Level 2: Screening Version 0.278	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green BabySeq Category A gene Phenotypes Hypertrophic osteoarthropathy, primary, autosomal dominant, MIM# 167100 Hypertrophic osteoarthropathy, primary, autosomal recessive 2, MIM# 614441
Red SLCO2A1 in BabyScreen+ newborn screening Level 2: Screening Version 1.113	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red BabySeq Category A gene Phenotypes Hypertrophic osteoarthropathy, primary, autosomal recessive 2, MIM# 614441 Hypertrophic osteoarthropathy, primary, autosomal dominant, MIM# 167100