APOB

apolipoprotein B
OMIM: 107730, Gene2Phenotype

8 panels

Panel Reviews Mode of inheritance Details
8 panels

Green APOB in Congenital Diarrhoea


Level 2: Gastroenterological disorders
Version 1.13

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hypobetalipoproteinemia, MIM# 615558

Green APOB in Incidentalome


Version 0.301

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Melbourne Genomics Health Alliance
  • Victorian Clinical Genetics Services
Phenotypes
  • Hypercholesterolemia, familial, 2, MIM# 144010
Tags
  • treatable

Green APOB in Additional findings_Adult


Level 2: Screening
Version 0.166

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Melbourne Genomics Health Alliance
Phenotypes
  • Hypercholesterolemia, familial, 2, MIM# 144010
Tags
  • treatable

Green APOB 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
    • Royal Melbourne Hospital
    • Expert Review Green
    Phenotypes
    • Hypobetalipoproteinemia, Hypercholesterolemia
    Tags
    • treatable

    Green APOB in Familial hypercholesterolaemia


    Level 2: Cardiovascular disorders
    Version 0.27

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

    Green APOB in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • BabySeq Category A gene
    Phenotypes
    • Hypercholesterolaemia, familial, 2, MIM# 144010
    • Hypobetalipoproteinaemia 615558

    Red APOB in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.114

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • BabySeq Category A gene
    Phenotypes
    • Hypercholesterolaemia, familial, 2, MIM# 144010
    Tags
    • for review
    • treatable

    Green APOB 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
    • Hypobetalipoproteinemia, Hypercholesterolemia