SLC26A4, solute carrier family 26 member 4, 5172

N. diseases: 194; N. variants: 174
Disease: Graves Disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.040 AlteredExpression disease BEFREE Recently, functional assays have shown a differential expression of SLC26A4 gene between Graves' disease (GD) and Hashimoto's thyroiditis (HT). 23280318 2013
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.040 AlteredExpression disease BEFREE The relative quantification using PDS transcript level among GD thyroid tissues was increased compared to normal thyroid tissues used as calibrator (mean: 27.17-fold higher than normal thyroid tissues). 21035230 2011
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.040 GeneticVariation disease BEFREE Here, by direct sequencing, we investigate the sequences of the 20 coding exons (2 to 21) of SLC26A4 and their flanking intron-exon junctions among patients affected with Graves' disease (GD) hyperthyroidism. 21045265 2010
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.040 Biomarker disease BEFREE Among cases, pendrin antibodies were more frequent and of higher titers in Hashimoto's thyroiditis than in Graves' disease. 19050049 2009