SLCO2A1

solute carrier organic anion transporter family member 2A1
OMIM: 601460
PanelMode of inheritanceDetails
3 panels
R-numbers: R167
Signed-off version 1.5
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Hypertrophic osteoarthropathy, primary, autosomal recessive 2, 614441
R-numbers: R15
Signed-off version 5.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Prostaglandin transporter deficiency
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 5.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Hypertrophic osteoarthropathy, primary, autosomal recessive 2 614441, Hypertrophic osteoarthropathy, primary, autosomal recessive 2 614441