SLC5A8, solute carrier family 5 member 8, 160728

N. diseases: 62; N. variants: 1
Disease: Well Differentiated Oligodendroglioma ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0751396
Disease: Well Differentiated Oligodendroglioma
Well Differentiated Oligodendroglioma 		0.010 PosttranslationalModification disease BEFREE Using an integrated approach for genome-wide methylation and copy number analyses, we identified SLC5A8 on chromosome 12q23.1 that was affected frequently by aberrant methylation in human astrocytomas and oligodendrogliomas. 15867356 2005