SCGN

secretagogin, EF-hand calcium binding protein
OMIM: 609202, Gene2Phenotype

1 panel

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


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

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • ulcerative colitis, MONDO:0005101