UCP2

uncoupling protein 2
OMIM: 601693, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber UCP2 in Congenital hyperinsulinism

Level 3: Disorders of unusual phenotypes
Level 2: Endocrine disorders
Version 3.4
Latest signed off version: v3.0 (22 Mar 2023)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Expert list
Phenotypes
  • Hyperinsulinism, MONDO:0002177
Tags
  • watchlist