ABCC3
ATP binding cassette subfamily C member 3
Theoretical — per Powers
Gene summary
A protein-coding gene on chromosome 17 (drug and xenobiotic transporters). 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.
Source: NCBI Gene, accessed 2026-10-07.
Protein reference (UniProt)
- Protein
ATP-binding cassette sub-family C member 3
- Function (excerpt)
ATP-dependent transporter of the ATP-binding cassette (ABC) family that hydrolyzes ATP to enable active transport of substrates conjugated with glucuronate, glutathione or sulfate. Operates at basolateral membranes of polarized cells such as hepatocytes and intestinal epithelial cells, where it mediates the efflux of conjugated substrates from intestine and liver into the bloodstream. Involved in enterohepatic recirculation of steroid glucuronates. Shares substrate specificity with MRP2, displaying higher affinity for both estrogen and androgen glucuronates such as 17beta-estradiol, estrone, testosterone and 5alpha-dihydrotestosterone glucuronates. Involved in sinusoidal efflux of mono- and bis-glucuronidated bilirubin from hepatocytes into the blood for renal uptake and excretion. May selectively transport steroid sulfate conjugates. Has transporter activity toward androgen sulfates such as androsterone and dehydroepiandrosterone sulfates but is inactive toward estrone 3-sulfate.
- Subcellular location
Basolateral cell membrane; Basal cell membrane.
- Tissue specificity
Mainly expressed in the liver. Also expressed in small intestine, colon, prostate, testis, brain and at a lower level in the kidney. In testis, localized to peritubular myoid cells, Leydig cells, along the basal membrane of Sertoli cells and moderately in the adluminal compartment of the seminiferous tubules.
Source: UniProtKB/Swiss-Prot O15438, release 2026_03, licensed CC BY 4.0. This is the protein’s normal biology, not evidence about post-drug syndromes; associated conditions are inherited disorders of the gene, not PFS, PSSD or PRSD.
Why its pathway is in the library
Transporters set systemic exposure to finasteride/SSRIs and clear conjugated steroid metabolites — directly relevant to both drug pharmacokinetics and Powers' clearance-centered PFS mechanism.
Written for the whole drug transporters family, not for ABCC3 specifically.
Powers’ note (his unpublished theorizing)
Powers named the ABCC transporter family (2026 summit interview, unpublished) as intracellular transporter genes implicated in metabolite clearance in his experimentally verifiable mechanism; individual ABCC members not separately named.
Narrative library record
Function
Basolateral membrane efflux pump (MRP3) of liver, intestine, kidney, adrenals, and pancreas that exports organic anions - bile constituents, bilirubin glucuronides, steroid conjugates - into blood for renal elimination; upregulated when ABCC2 fails, showing the two pumps compensate for each other.
Corpus relevance
The second transporter in Powers' DWP-002 export chain; its basolateral position makes it the backup route for conjugated androgens when apical export is impaired. Attribution: theoretical-per-Powers.
Mentioned in 4 corpus records
- Gene recordPowers’ theory
UGT1A1 — UDP glucuronosyltransferase family 1 member A1
chromosome 2 (2q37 region; 233.76-233.77 Mb GRCh38)
UDP-glucuronosyltransferase that conjugates glucuronic acid onto lipophilic molecules - steroids, bilirubin, hormones, drugs - converting them to water-soluble, excretable metabolites. Over 100 described variants alter its activity (for example, Gilbert…
ABCC2ABCC3UGT1A1UGT2B15UGT2B17+1GENE-UGT1A1PFSCore corpus - Gene recordPowers’ theory
Steroid-glucuronidating enzyme of extrahepatic tissues (notably prostate) that conjugates C19 steroids including DHT, androsterone, and 3-alpha-diol; notable for common copy-number variation (whole-gene deletion is frequent) associated in the literature with…
ABCC3UGT1A1UGT2B15UGT2B17UGT2B7GENE-UGT2B17PFSCore corpus - Gene recordPowers’ theory
Apical membrane efflux pump (MRP2) of liver, kidney, and intestine that exports organic anions - including bilirubin glucuronides and drug conjugates - out of cells for elimination. Loss causes Dubin-Johnson syndrome; polymorphisms alter drug pharmacokinetics.
ABCC2ABCC3UGT1A1UGT2B15UGT2B17GENE-ABCC2Core corpus - Gene recordPowers’ theory
Encodes OATP1B1, the sodium-independent organic-anion transporter on liver cell membranes that moves bilirubin, hormones, toxins, and many drugs from blood into the liver for clearance; biallelic loss together with SLCO1B3 causes Rotor syndrome (conjugated…
ABCC2ABCC3SLCO1B1SLCO1B3UGT1A1+2GENE-SLCO1B1PFSCore corpus
Also in drug and xenobiotic transporters
All 62 genes- SLC6A4
solute carrier family 6 member 4
chr 17· Drug transporters· 10 records - ABCC2Powers
ATP binding cassette subfamily C member 2
chr 10· Drug transporters· 6 records - ABCB1
ATP binding cassette subfamily B member 1
chr 7· Drug transporters· 3 records - ABCC5Powers
ATP binding cassette subfamily C member 5
chr 3· Drug transporters· 3 records - SLCO1B1Powers
solute carrier organic anion transporter family member 1B1
chr 12· Drug transporters· 4 records - SLC18A2
solute carrier family 18 member A2
chr 10· Drug transporters· 1 record - SLCO1B3
solute carrier organic anion transporter family member 1B3
chr 12· Drug transporters· 1 record - ABCB11
ATP binding cassette subfamily B member 11
chr 2· Drug transporters· Pathway candidate
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