Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C3149462
Disease: HYPERALPHALIPOPROTEINEMIA 1
HYPERALPHALIPOPROTEINEMIA 1 		0.800 GeneticVariation UNIPROT Cholesteryl ester transfer protein (CETP) deficiency is one of the most important and common causes of hyperalphalipoproteinemia (HALP) in the Japanese. 12091484

2002
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C3149462
Disease: HYPERALPHALIPOPROTEINEMIA 1
HYPERALPHALIPOPROTEINEMIA 1 		0.800 GeneticVariation UNIPROT A missense mutation in the cholesteryl ester transfer protein gene with possible dominant effects on plasma high density lipoproteins. 8408659

1993
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C3149462
Disease: HYPERALPHALIPOPROTEINEMIA 1
HYPERALPHALIPOPROTEINEMIA 1 		0.800 GeneticVariation UNIPROT We recently described a Japanese family with increased HDL levels and CETP deficiency due to a splicing defect of the CETP gene. 2215607

1990