SLC10A2, solute carrier family 10 member 2, 6555

N. diseases: 66; N. variants: 9
Disease: Hypertriglyceridemia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.020 AlteredExpression phenotype BEFREE And bioinformatics studies discovered that the expression of slc10a2 was increased in high-grade hypertriglyceridemia patients. 29642873 2018
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.020 AlteredExpression phenotype BEFREE We conclude that impaired absorption of bile acid in type IV hypertriglyceridemia results from diminished expression of the ASBT gene in terminal ileum. 10974045 2000