APOC3

apolipoprotein C3
OMIM: 107720, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red APOC3 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Apolipoprotein C-III deficiency MIM#614028

Red APOC3 in Dyslipidaemia


Level 2: Endocrine disorders
Version 0.41

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Red
    • Royal Melbourne Hospital
    Phenotypes
    • Apolipoprotein C-III deficiency MIM#614028