Matches in DBpedia 2014 for { <http://dbpedia.org/resource/SLC22A18> ?p ?o. }
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- SLC22A18 abstract "Solute carrier family 22 member 18 is a protein that in humans is encoded by the SLC22A18 gene.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 may play a role in malignancies and disease that involve this region as well as the transport of chloroquine- and quinidine-related compounds in the kidney. Two alternative transcripts encoding the same isoform have been described.".
- SLC22A18 entrezgene "5002".
- SLC22A18 wikiPageID "15062953".
- SLC22A18 wikiPageRevisionID "593059460".
- SLC22A18 hasPhotoCollection SLC22A18.
- SLC22A18 requireManualInspection "no".
- SLC22A18 summaryText "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 may play a role in malignancies and disease that involve this region as well as the transport of chloroquine- and quinidine-related compounds in the kidney. Two alternative transcripts encoding the same isoform have been described.".
- SLC22A18 updateCitations "yes".
- SLC22A18 updatePage "yes".
- SLC22A18 updateProteinBox "yes".
- SLC22A18 updateSummary "yes".
- SLC22A18 subject Category:Solute_carrier_family.
- SLC22A18 type Biomolecule.
- SLC22A18 type Protein.
- SLC22A18 type BiologicalObject.
- SLC22A18 comment "Solute carrier family 22 member 18 is a protein that in humans is encoded by the SLC22A18 gene.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.".
- SLC22A18 label "SLC22A18".
- SLC22A18 sameAs m.03hg6xx.
- SLC22A18 sameAs Q17148547.
- SLC22A18 sameAs Q17148547.
- SLC22A18 sameAs SLC22A18.
- SLC22A18 wasDerivedFrom SLC22A18?oldid=593059460.
- SLC22A18 isPrimaryTopicOf SLC22A18.