FABP2, fatty acid binding protein 2, 2169

N. diseases: 65; N. variants: 2
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.070 GeneticVariation phenotype BEFREE The Ala54Thr polymorphism of FABP2 was associated with high triglycerides levels, but not to GSD; suggesting that environmental factors modulate such susceptibility. 26019038 2016
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.070 GeneticVariation phenotype BEFREE LPL p.474X and FABP2 p.55T were associated with decreased total cholesterol and LDL-C, respectively; APOA5 p.19W with increased HDL-C; APOA5 p.19W and FABP2 p.55T with increased triglycerides; and APOB p.4181K and LDLR c.1959T with decreased triglycerides. 25587205 2014
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.070 GeneticVariation phenotype BEFREE Twenty-three FABP2 Ala54 and 23 Thr54 carriers with hypertriglyceridemia (triacylglycerol level >200mg/dL) were enrolled in this study. 20080390 2011
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.070 GeneticVariation phenotype BEFREE Thr54 allele carriers of the Ala54Thr variant of FABP2 gene have associations with metabolic syndrome and hypertriglyceridemia in urban South Indians. 16919542 2006
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.070 GeneticVariation phenotype BEFREE Alanine-for-threonine substitution at codon 54 (A54T polymorphism) in the fatty acid-binding protein 2 gene (FABP2) has been associated with hypertriglyceridemia and insulin resistance. 16908951 2006
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.070 GeneticVariation phenotype LHGDN Our study suggests that the effects of FABP2 allelic variations on lipid traits are context dependent, indicating that this variant may play an important role in cardiovascular pathogenesis in the presence of IRS or hypertriglyceridemia. 15547295 2005
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.070 GeneticVariation phenotype BEFREE Our study suggests that the effects of FABP2 allelic variations on lipid traits are context dependent, indicating that this variant may play an important role in cardiovascular pathogenesis in the presence of IRS or hypertriglyceridemia. 15547295 2005
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.070 GeneticVariation phenotype BEFREE In conclusion, in contrast to type 2, type 1 diabetes does not interact with the codon 54 polymorphism of the fatty acid binding protein 2 gene to cause hypertriglyceridemia/dyslipidemia. 12161503 2002