SLC10A2, solute carrier family 10 member 2, 6555

N. diseases: 66; N. variants: 9
Disease: Bile acid malabsorption ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2747802
Disease: Bile acid malabsorption
Bile acid malabsorption 		0.040 AlteredExpression disease BEFREE Irinotecan-induced bile acid malabsorption is associated with down-regulation of ileal Asbt (Slc10a2) in mice. 28288854 2017
CUI: C2747802
Disease: Bile acid malabsorption
Bile acid malabsorption 		0.040 GeneticVariation disease BEFREE No ASBT mutations were identified and the ASBT gene did not segregate with the bile acid malabsorption phenotype. 17171805 2006
CUI: C2747802
Disease: Bile acid malabsorption
Bile acid malabsorption 		0.040 GeneticVariation disease BEFREE ASBT gene polymorphisms were detected in 5 of the 13 adult IBAM patients. 11589382 2001
CUI: C2747802
Disease: Bile acid malabsorption
Bile acid malabsorption 		0.040 GeneticVariation disease BEFREE Inherited mutation of ASBT leads to congenital diarrhea secondary to bile acid malabsorption. 11396803 2001