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SLC10A1

solute carrier family 10 member 1
2 disorders 1 no genetic record 1 causative 14q24.1 gene with protein product
HGNC:10905MonarchNCBI Gene 6554ENSG00000100652UniProt Q14973OMIM 182396

Aliases: NTCP, NTCP1.

In the knowledge base · computed from kb/ at build time

Disorders

Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.

DisorderRelationshipWhere the gene appears
Hypercholanemia Familial 2 causative germline loss of function
mechanism: NTCP Loss from the Hepatocyte Basolateral Membrane
Hepatitis D no genetic record
mechanism: HBsAg-Dependent Hepatocyte Entry via NTCP
Mechanism modules · computed from kb/

Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.