SLC10A1 (NTCP): Sodium-Taurocholate Cotransporting Polypeptide

Key bile acid transporter and hepatitis B/D virus receptor

Gene Information Card

Symbol SLC10A1
Full Name Solute Carrier Family 10 Member 1
Gene Type Protein coding
Chromosomal Location 14q24.1
NCBI Gene ID 6554 ncbi.nlm.nih.gov/gene/6554
Ensembl ID ENSG00000170652
UniProt ID Q14973
OMIM ID 182396
HGNC ID 10905
Aliases NTCP, NTCP1, GIG29

Description

SLC10A1 encodes the sodium-taurocholate cotransporting polypeptide (NTCP), a transmembrane protein primarily expressed in the liver. NTCP mediates the uptake of bile acids from portal blood into hepatocytes, playing a critical role in enterohepatic circulation. It also serves as the cellular receptor for hepatitis B and D viruses, facilitating viral entry into hepatocytes.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Hypercholanemia, familial Loss-of-function mutations in SLC10A1 impair bile acid transport, leading to elevated serum bile acid levels. OMIM 182396; PMID 25557789
Hepatitis B virus infection NTCP acts as the receptor for HBV; polymorphisms may affect susceptibility or response to infection. PMID 23149947; PMID 25557789
Hepatitis D virus infection HDV requires NTCP for entry; NTCP expression is essential for co-infection with HBV. PMID 23149947
Cholestasis Reduced NTCP function can contribute to cholestatic liver disease, though SLC10A1 mutations are rare. PMID 25557789

Expression Profile

Tissue Expression
Tissue nTPM level
Liver High (nTPM ~ 200) Predominant expression in hepatocytes
Kidney Low (nTPM ~ 5) Minimal expression in renal tubules
Small intestine Low (nTPM ~ 3) Low expression in enterocytes
Other tissues Not detected No significant expression
Cell Line Expression
Cell Line nTPM Notes
HepG2 High Hepatocellular carcinoma cell line
Huh7 High Hepatoma cell line
HEK293 Low When overexpressed, used for functional studies
Caco-2 Low Colorectal adenocarcinoma cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
p.Ser267Phe Missense Rare (allele frequency <0.1%) Loss of bile acid transport; reduces HBV entry
p.Arg252His Missense Rare Impaired transport activity
p.Ile223Thr Missense Rare Reduced cell surface expression
p.Leu294Trp Missense Rare Loss of function
Mutation functional classification

Loss of Function (LOF)

Most SLC10A1 mutations result in loss of bile acid transport function, leading to hypercholanemia.

Gain of Function (GOF)

No gain-of-function mutations reported.

Dominant Negative (DN)

No dominant-negative effects described; disease is typically autosomal recessive.

Gene Ontology (GO)

bile acid:sodium symporter activity (GO:0008508) symporter activity (GO:0015293)
• integral component of membrane (GO:0016021) • integral component of plasma membrane (GO:0005887)
bile acid metabolic process (GO:0008203) bile acid transport (GO:0015721)

Pathways

Bile acid transport and enterohepatic circulation
Hepatitis B virus entry into hepatocytes

Protein Summary

NTCP is a 349-amino acid protein with seven transmembrane domains. It functions as a symporter, coupling sodium ion influx to bile acid uptake. The protein is heavily glycosylated and localized to the basolateral membrane of hepatocytes. Its structure includes a large extracellular loop that is critical for HBV receptor function.

Related Products

Product name Cat.No. Species Gene ID
SLC10A1 Knockout HEK293 Cell Line EDJ-KQ2393 Human 6554 Details Get a Quote
SLC10A1 Knockout HeLa Cell Line EDJ-KQ54503 Human 6554 Details Get a Quote
SLC10A1 Knockout A-549 Cell Line EDJ-KQ62988 Human 6554 Details Get a Quote
SLC10A1 Knockout HCT 116 Cell Line EDJ-KQ71459 Human 6554 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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