APOC2

apolipoprotein C2
OMIM: 608083, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green APOC2 in Mendeliome


Version 1.2789

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hyperlipoproteinemia, type Ib MIM#207750

Amber APOC2 in Amyloidosis


Version 1.1

Component of the following Super Panels:

  • Kidneyome_SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • APOC2-related amyloidosis, MONDO:0019065

    Green APOC2 in Dyslipidaemia


    Level 2: Endocrine disorders
    Version 0.45

    Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Hyperlipoproteinemia, type Ib MIM#207750

    Green APOC2 in Transplant Co-Morbidity Superpanel


    Level 2: Screening
    Version 0.18

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Hyperlipoproteinemia, type Ib MIM#207750