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GeneQ17907816· pop 5· linked from 98 articles

Also known as ABC30, CMOAT, DJS, MRP2, cMRP, Multidrug resistance-associated protein 2, ATP binding cassette subfamily C member 2

gene da espécie Homo sapiens

In the Vinony graph

Within Vinony's link graph, ABCC2 is referenced by 98 other articles, and connects out to ion, PubMed and endothelium.

It is catalogued under topics including ATP-binding cassette transporters and Genes on human chromosome 10.

Its subject is documented across 4 Wikipedia language editions.

Gene data

ABCC2
Name
ATP binding cassette subfamily C member 2
Type
protein-coding
Position
99,782,640–99,853,670 (+)
Aliases
ABC30, CMOAT, DJS, MRP2, cMRP
RefSeq RNA
NM_000392.5, XM_006717630.4, XM_006717631.5, XM_011539291.4, XM_017015675.3
RefSeq protein
NP_000383.2, XP_006717693.1, XP_006717694.1, XP_011537593.1, XP_016871164.1

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].

via MyGene.info

Gene · Ensembl

ATP binding cassette subfamily C member 2

Symbol
ABCC2
Biotype
Protein coding
Organism
Homo sapiens
Location
10:99,782,640-99,853,670
Strand
Forward (+)
Assembly
GRCh38
View on Ensembl →

via Ensembl · EMBL-EBI

Research

2,464 papers

via PubMed

Wikidata facts

Instance of
gene
Show 9 more facts
HomoloGene ID
68052
found in taxon
Homo sapiens
genomic end
99852594
genomic start
99782640
cytogenetic location
10q24.2
genetic association
Dubin-Johnson syndrome
expressed in
sural nerve
Sources (7)

via Wikidata · CC0

Available in 4 languages

via Wikidata sitelinks · CC0

Connections

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