Gene: SLC26A4 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4 		0.300 Biomarker disease CTD_human The H723R mutation in the PDS/SLC26A4 gene is associated with typical Pendred syndrome in Korean patients. 17322586 2006
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4 		0.300 Biomarker disease CTD_human Molecular analysis of the PDS gene in a nonconsanguineous Sicilian family with Pendred's syndrome. 16053392 2005
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4 		0.300 Biomarker disease CTD_human Mutations in the SLC26A4 (pendrin) gene in patients with sensorineural deafness and enlarged vestibular aqueduct. 15279074 2004