1. Genes and Genomic Entities
  2. CELSR2

CELSR2

cadherin EGF LAG seven-pass G-type receptor 2
OMIM: 604265, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red CELSR2 in Severe hypertriglyceridaemia

Level 3: Arteriopathies
Level 2: Cardiovascular disorders
Version 1.17

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Other
Phenotypes
  • hypertriglyceridaemia
Red CELSR2 in Familial hypercholesterolaemia

Level 3: Arteriopathies
Level 2: Cardiovascular disorders
Version 1.30

review Not set
Sources
  • Eligibility statement prior genetic testing
Phenotypes
  • Gene part of the Global Lipid Genetic Consortium 12-SNP LDL-C gene score calculation (Talmud et al, 2013)
  • Gene part of the 6-SNP LDL-C gene score calculation (Futema et al, 2015)