APOC2

apolipoprotein C2
OMIM: 608083, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green APOC2 in Mendeliome


Version 2.22

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

Amber APOC2 in Amyloidosis


Version 2.0

Component of the following Super Panels:

  • Kidneyome_SuperPanel
  • 1 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; Cardiovascular disorders
    Version 1.0

    Component of the following Super Panels:

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

    Green APOC2 in Transplant Co-Morbidity


    Level 2: Screening
    Version 1.0

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