UCP2

uncoupling protein 2
OMIM: 601693, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Amber UCP2 in Hyperinsulinism


Level 2: Endocrine disorders
Version 1.16

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Hyperinsulinism

Amber UCP2 in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • {Obesity, susceptibility to, BMIQ4} 607447
  • Hyperinsulinism

Red UCP2 in Additional findings_Paediatric


Level 2: Screening
Version 0.278

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • BabySeq Category C gene
Phenotypes
  • Hyperinsulinism

Red UCP2 in BabyScreen+ newborn screening


Level 2: Screening
Version 1.113

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • BabySeq Category C gene
  • BeginNGS
Phenotypes
  • Hyperinsulinism, ORPHA:276556
  • Hyperinsulinism