PanelApp (stage)
  1. Genes and Genomic Entities
  2. APOA1

APOA1

apolipoprotein A1
OMIM: 107680, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green APOA1 in Vasculitis


Level 2: Immunological disorders
Version 0.82

review Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green APOA1 in Mendeliome


Version 1.1891

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Amyloidosis, hereditary systemic 3, MIM# 620657
  • Amyloidosis, 3 or more types MIM#105200
  • Hypoalphalipoproteinemia, primary, 2 MIM#618463
  • Hypoalphalipoproteinemia, primary, 2, intermediate MIM#619836

Green APOA1 in Renal Amyloidosis


Level 2: Renal and urinary tract disorders
Version 0.22

Component of the following Super Panels:

  • Kidneyome_SuperPanel

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Amyloidosis, 3 or more types, MIM#105200

    Green APOA1 in Dyslipidaemia


    Level 2: Endocrine disorders
    Version 0.41

    Component of the following Super Panels:

  • Metabolic Disorders Superpanel

    		•  review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Hypoalphalipoproteinaemia, primary, 2, intermediate, MIM# 619836

    Green APOA1 in Hereditary Neuropathy - complex


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.14

    Component of the following Super Panels:

  • Hereditary Neuropathy_CMT_IsolatedAndComplex
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • NHS GMS
    Phenotypes
    • Amyloidosis, 3 or more types 105200
    • Renal failure, Axonal sensory-motor neuropathy, amyloid nephropathy

    Green APOA1 in Transplant Co-Morbidity Superpanel


    Level 2: Screening
    Version 0.18

    		review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Hypoalphalipoproteinaemia, primary, 2, intermediate, MIM# 619836