GPR15

G protein-coupled receptor 15
OMIM: 601166, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber GPR15 in Primary immunodeficiency or monogenic inflammatory bowel disease


Level 2: Immunology
Version 9.102
Latest signed off version: v9.91 (12 Aug 2026)

review BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • inflammatory bowel disease, MONDO:0005265
Tags
  • Q3_26_promote_green