Selected-GenAtlas references SOURCE GeneCards NCBI Gene Swiss-Prot Orphanet Ensembl
HGNC UniGene Nucleotide OMIM UCSC
Home Page
FLASH GENE
Symbol APOA1 contributors: mct/npt - updated : 08-02-2019
HGNC name apolipoprotein A-I
HGNC id 600
ASSOCIATED DISORDERS
corresponding disease(s) NNHA , CCLD
Susceptibility
  • to premature atherosclerosis and to low HDL-cholesterol
  • to premature coronary artery disease
  • Variant & Polymorphism other
  • deletion in exon 3 causing a frameshift and heterozygosity for a nucleotide substitution in exon 4 (T>G, L141R) increasing the risk of low HDL-cholesterol
  • mutation L178P leads to endothelial dysfunction, increased arterial wall thickness, and premature coronary artery disease
  • Candidate gene
    Marker
    Therapy target
    ANIMAL & CELL MODELS