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10 sources retrieved · Most recent: April 2026 · Index updated 15 days ago
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ABCC11
ATP binding cassette subfamily C member 11
Chromosome 16 · 16q12.1
NCBI Gene: 85320Ensembl: ENSG00000121270.16HGNC: HGNC:14639UniProt: Q96J66
68PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLE
Transporter
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
purine nucleotide transmembrane transporter activityABC-type glutathione S-conjugate transporter activityapical plasma membraneABC-type bile acid transporter activitybreast fibrocystic diseaseperipheral neuropathydementiapernicious anemia
✦AI Summary

ABCC11 encodes an ATP-dependent transporter of the ABC family that actively extrudes physiological compounds and xenobiotics from cells 1. The transporter mediates efflux of diverse lipophilic anions including glutathione S-conjugates (leukotriene C4), steroid sulfates (DHEAS, estrone 3-sulfate), glucuronides (estradiol 17-beta-D-glucuronide), bile acids (glycocholate, taurocholate), cyclic nucleotides (cAMP, cGMP), and chemotherapeutic agents like methotrexate and 5-fluorouracil 1. A critical non-synonymous SNP 538G>A (Gly180Arg) dramatically affects ABCC11 function, with the variant protein undergoing proteasomal degradation due to misfolding 2. This polymorphism determines earwax type: wild-type (G allele) produces wet earwax while the variant (A allele) produces dry earwax 23. ABCC11 plays essential roles in apocrine gland secretion, including transport of odorant precursors that contribute to axillary osmidrosis when metabolized by skin bacteria 45. The transporter also influences ear canal microbiota composition through genome-microbiome interactions 6. Clinically, ABCC11 polymorphisms serve as biomarkers for predicting chemotherapy efficacy, particularly for nucleoside-based anticancer drugs, and for diagnosing axillary osmidrosis 23.

Sources cited
1
ABCC11 is an ATP-dependent transporter that effluxes diverse lipophilic anions including steroids, bile acids, and chemotherapeutic agents
PMID: 16868766
2
The 538G>A SNP causes protein misfolding and degradation, affecting earwax type and chemotherapy response
PMID: 21182469
3
ABCC11 genotyping serves as clinical diagnostic tool for axillary osmidrosis
PMID: 27057547
4
ABCC11 transports odorant precursors that are metabolized by skin bacteria to produce body odor
PMID: 39543265
5
ABCC11 polymorphism affects apolipoprotein D expression in apocrine glands
PMID: 25633187
6
ABCC11 polymorphisms regulate ear canal microbiota composition through genome-microbiome interactions
PMID: 39817749
Disease Associationsⓘ20
breast fibrocystic diseaseOpen Targets
0.35Weak
peripheral neuropathyOpen Targets
0.30Weak
dementiaOpen Targets
0.29Weak
pernicious anemiaOpen Targets
0.28Weak
breast ductal adenocarcinomaOpen Targets
0.11Weak
rheumatoid arthritisOpen Targets
0.09Suggestive
breast cancerOpen Targets
0.09Suggestive
coronary artery diseaseOpen Targets
0.08Suggestive
esophageal diseaseOpen Targets
0.07Suggestive
juvenile idiopathic arthritisOpen Targets
0.07Suggestive
COVID-19Open Targets
0.07Suggestive
intrahepatic cholangiocarcinomaOpen Targets
0.07Suggestive
infectionOpen Targets
0.06Suggestive
SepsisOpen Targets
0.06Suggestive
acute respiratory distress syndromeOpen Targets
0.05Suggestive
gestational diabetesOpen Targets
0.05Suggestive
neoplasmOpen Targets
0.05Suggestive
Myocardial IschemiaOpen Targets
0.04Suggestive
serum lipopolysaccharide activityOpen Targets
0.04Suggestive
cancerOpen Targets
0.04Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
ABCC10Shared pathway60%ABCC3Shared pathway38%SLC22A8Shared pathway33%SLCO1A2Shared pathway33%SLCO1B3Shared pathway29%SLC22A10Shared pathway25%
Tissue Expression6 tissues
Liver
100%
Brain
10%
Bone Marrow
5%
Heart
3%
Ovary
2%
Lung
1%
Gene Interaction Network
Click a node to explore
ABCC11ABCC10ABCC3SLC22A8SLCO1A2SLCO1B3SLC22A10
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted · UniProt Q96J66
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
1.00LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.87 [0.75–1.00]
RankingsWhere ABCC11 stands among ~20K protein-coding genes
  • #6,872of 20,598
    Most Researched68
  • #9,727of 17,882
    Most Constrained (LOEUF)1.00
Genes detectedABCC11
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Diagnosis of Human Axillary Osmidrosis by Genotyping of the Human ABCC11 Gene: Clinical Practice and Basic Scientific Evidence.
PMID: 27057547
Biomed Res Int · 2016
1.00
2
Pharmacogenomics of human ABC transporter ABCC11 (MRP8): potential risk of breast cancer and chemotherapy failure.
PMID: 21182469
Anticancer Agents Med Chem · 2010
0.90
3
Interplay of human ABCC11 transporter gene variants with axillary skin microbiome functional genomics.
PMID: 39543265
Sci Rep · 2024
0.80
4
ABCC10, ABCC11, and ABCC12.
PMID: 16868766
Pflugers Arch · 2007
0.70
5
Association between the
PMID: 39817749
Microbiol Spectr · 2025
0.60