SLCO2A1

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

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green SLCO2A1 in Inflammatory bowel disease Level 2: Gastroenterological disorders Version 0.122 Component of the following Super Panels: Immunological disorders_SuperPanel	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Inflammatory bowel disease, MONDO:0005265, SLCO2A1-related Enteropathy
Green SLCO2A1 in Mendeliome Version 1.2302	1 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 0.302	1 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	1 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 1.116	1 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