LDLRAP1

low density lipoprotein receptor adaptor protein 1
OMIM: 605747, Gene2Phenotype

7 panels

Panel Reviews Mode of inheritance Details
7 panels

Green LDLRAP1 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hypercholesterolemia, familial, 4, MIM# 603813

Green LDLRAP1 in Dyslipidaemia


Level 2: Endocrine disorders
Version 0.41

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Hypercholesterolemia, familial, 4, MIM# 603813

    Green LDLRAP1 in Familial hypercholesterolaemia


    Level 2: Cardiovascular disorders
    Version 0.27

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Hypercholesterolemia, familial, 4, MIM# 603813

    Green LDLRAP1 in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.109

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Hypercholesterolemia, familial, autosomal recessive, 603813 (3)

    Green LDLRAP1 in Prepair 1000+


    Level 2: Screening
    Version 1.9

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Hypercholesterolemia, familial, autosomal recessive, 603813 (3)

    Green LDLRAP1 in Transplant Co-Morbidity Superpanel


    Level 2: Screening
    Version 0.18

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Hypercholesterolemia, familial, 4, MIM# 603813

    Green LDLRAP1 in Prepair 500+


    Level 2: Screening
    Version 1.1

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Hypercholesterolemia, familial, autosomal recessive, 603813 (3)