Prostate Cancer Ontology
Center for Systems Biology, Sichuan University West China Hospital, Sichuan China
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折叠 Prostate cancerProstate cancer
折叠 Epidemiological aspects of prostate cancerEpidemiological aspects of prostate cancer
展开 Basic information of patientBasic information of patient
展开 Personal medical historyPersonal medical history
折叠 Genetic and epigenetic of prostate cancerGenetic and epigenetic of prostate cancer
展开 Lifestyles of prostate cancerLifestyles of prostate cancer
展开 Diagnostic aspects of prostate cancerDiagnostic aspects of prostate cancer
展开 Therapeutic aspects of prostate cancerTherapeutic aspects of prostate cancer
SLC22A18
Preferred Name SLC22A18 solute carrier family 22 member 18
Definition This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene is imprinted, with preferential expression from the maternal allele. Mutations in this gene have been found in Wilms' tumor and lung cancer. This protein may act as a transporter of organic cations, and have a role in the transport of chloroquine and quinidine-related compounds in kidney. Several alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Oct 2015]
Synonyms & Abbreviations HET; ITM; BWR1A; IMPT1; TSSC5; ORCTL2; BWSCR1A; SLC22A1L; p45-BWR1A
ReferenceCode Location: 11p15.4; Sequence: Chromosome: 11; NC_000011.10 (2899721..2925246)
ReferenceURL https://www.ncbi.nlm.nih.gov/gtr/genes/5002/
PMID NA
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