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GENE - CHEMICAL INTERACTIONS REPORT

RGD ID: 1603576
Species: Homo sapiens
RGD Object: Gene
Symbol: SLC47A2
Name: solute carrier family 47 member 2
Acc ID: CHEBI:8776
Term: ranitidine
Definition: A member of the class of furans used to treat peptic ulcer disease (PUD) and gastroesophageal reflux disease.
Chemical ID: MESH:D011899
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
SLC47A2multiple interactionsEXP 6480464CTDRanitidine inhibits the reaction [SLC47A2 protein results in increased uptake of 1-Methyl-4-phenylpyridinium]PMID:22419765
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