IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, SLC22A1L
Definition : Molecular assay reagents intended to identify mutations in the solute carrier family 22 (organic cation transporter), member 18 (SLC22A1L) gene, located at chromosome 11p15.5, which may be involved in malignancies and disease that involve the 11p15.5 tumor suppressor gene region as well as the transport of chloroquine- and quinidine-related compounds in the kidney. Anomalies in this gene are associated with several malignances and diseases, including Beckwith-Wiedemann syndrome.
Entry Terms : "Beckwith-Widemann Syndrome Gene Mutation Reagents" , "Solid Cancer Tumor Gene Mutation Reagents" , "SCC22A1L Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, SLC22A1L"
UMDC code : 24968