ABCB4, ATP binding cassette subfamily B member 4, 5244
N. diseases: 157; N. variants: 65
Source: ALL
Disease | Score gda | Association Type | Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
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0.300 | Biomarker | disease | BEFREE | In addition, messenger RNA (mRNA) levels of multidrug resistance P-glycoprotein 3 (MDR3 Pgp) and phosphatidylcholine transfer protein (PCTP) were markedly low in the liver specimens compared with the levels in specimens of control subjects, gallbladder stone patients, and patients with obstructive cholestasis. | 11343249 | 2001 | ||||
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0.300 | GeneticVariation | disease | BEFREE | Because phospholipids are a carrier and a solvent of cholesterol in hepatic bile, we hypothesized that a defect in the MDR3 gene could be the genetic basis for peculiar forms of cholesterol gallstone disease, in particular those associated with symptoms and cholestasis without evident common bile duct stone. | 11313316 | 2001 | ||||
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0.300 | Biomarker | disease | RGD | Phospholipid alterations in hepatocyte membranes and transporter protein changes in cholestatic rat model. | 11680581 | 2001 | ||||
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0.300 | AlteredExpression | disease | BEFREE | In mice with various expression levels of Mdr2 or MDR3, the human homolog of Mdr2, we observed that the plasma level of cholesterol and phospholipid during cholestasis correlated very closely with the expression level of these canalicular P-glycoproteins. | 9802889 | 1998 | ||||
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0.300 | AlteredExpression | disease | BEFREE | Among the hereditary human cholestasis, a subtype of progressive familial intrahepatic cholestasis with high gamma-glutamyltranspeptidase (GGT) serum activity shares histological, biochemical, and genetic features with mice lacking mdr2 gene expression (mdr2 -/- mice). | 8666348 | 1996 | ||||
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0.300 | Biomarker | disease | MGD |