ABCC2 Chromosome 10

ATP binding cassette subfamily C member 2
246 variants 246 Health Risk

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What This Gene Does
The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. This protein is expressed in the canalicular (apical) part of the hepatocyte and functions in biliary transport. Substrates include anticancer drugs such as vinblastine; therefore, this protein appears to contribute to drug resistance in mammalian cells. Several different mutations in this gene have been observed in patients with Dubin-Johnson syndrome (DJS), an autosomal recessive disorder characterized by conjugated hyperbilirubinemia. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
ATP binding cassette subfamily C
Locus Type
gene with protein product
Location
10q24.2
Ensembl
ENSG00000023839
Associated Conditions (12)
Dubin-Johnson syndrome
ABCC2-related disorder
Acute myeloid leukemia
Melanoma
Familial cancer of breast
Hepatocellular carcinoma
Inborn genetic diseases
Colon adenocarcinoma
Thyroid cancer
nonmedullary
1
Autosomal recessive inherited pseudoxanthoma elasticum
Key Variants
All Variants (246)
RSID Category Clinical Significance Conditions
RS2038785200 Health Risk Likely pathogenic
RS2133124899 Health Risk Likely pathogenic Dubin-Johnson syndrome, Dubin-Johnson syndrome
RS2492841473 Health Risk Likely pathogenic
RS2492843794 Health Risk Likely pathogenic
RS2492846710 Health Risk Likely pathogenic
RS2492919806 Health Risk Likely pathogenic
RS2492926991 Health Risk Likely pathogenic ABCC2-related disorder, ABCC2-related disorder
RS2492968753 Health Risk Likely pathogenic
RS2493011181 Health Risk Likely pathogenic
RS2493019052 Health Risk Likely pathogenic
RS2493048479 Health Risk Likely pathogenic
RS533334893 Health Risk Likely pathogenic Dubin-Johnson syndrome, Dubin-Johnson syndrome
RS72558202 Health Risk Likely pathogenic Dubin-Johnson syndrome, ABCC2-related disorder, Dubin-Johnson syndrome
RS753329079 Health Risk Likely pathogenic ABCC2-related disorder, ABCC2-related disorder
RS756707816 Health Risk Likely pathogenic
RS763527398 Health Risk Likely pathogenic
RS765064597 Health Risk Likely pathogenic
RS781481868 Health Risk Likely pathogenic ABCC2-related disorder, Colon adenocarcinoma, Thyroid cancer
RS781545154 Health Risk Likely pathogenic
RS1045996985 Health Risk Pathogenic Dubin-Johnson syndrome, Dubin-Johnson syndrome
RS1158274146 Health Risk Pathogenic
RS1161530285 Health Risk Pathogenic
RS1207538473 Health Risk Pathogenic
RS1208873596 Health Risk Pathogenic
RS1226153645 Health Risk Pathogenic
RS1257076487 Health Risk Pathogenic
RS1261223764 Health Risk Pathogenic
RS1280917011 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1313391525 Health Risk Pathogenic
RS1314486961 Health Risk Pathogenic
RS1333544687 Health Risk Pathogenic
RS1347233847 Health Risk Pathogenic
RS1351419381 Health Risk Pathogenic Dubin-Johnson syndrome, Dubin-Johnson syndrome
RS1393497113 Health Risk Pathogenic
RS1454680088 Health Risk Pathogenic
RS145715632 Health Risk Pathogenic Dubin-Johnson syndrome, Dubin-Johnson syndrome
RS1554845888 Health Risk Pathogenic ABCC2-related disorder, ABCC2-related disorder
RS1554849397 Health Risk Pathogenic
RS1554851699 Health Risk Pathogenic
RS1554853026 Health Risk Pathogenic
RS1554854612 Health Risk Pathogenic
RS1564674618 Health Risk Pathogenic
RS1564687941 Health Risk Pathogenic ABCC2-related disorder, ABCC2-related disorder
RS1564688595 Health Risk Pathogenic
RS1564695476 Health Risk Pathogenic
RS1564701009 Health Risk Pathogenic
RS1564702358 Health Risk Pathogenic
RS1590192032 Health Risk Pathogenic Dubin-Johnson syndrome, Dubin-Johnson syndrome
RS17222547 Health Risk Pathogenic ABCC2-related disorder, ABCC2-related disorder
RS183923599 Health Risk Pathogenic
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