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 8.78
Latest signed off version: v8.0 (30 Apr 2025)

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