Gene: CLDN19 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 149461
Gene Symbol: CLDN19
CLDN19 		0.020 GeneticVariation disease BEFREE Patients with mutations in the CLDN19 gene also present severe visual impairment. 23301036 2013
Entrez Id: 149461
Gene Symbol: CLDN19
CLDN19 		0.020 Biomarker disease BEFREE The identification of CLDN19 mutations in patients with chronic renal failure and severe visual impairment supports the fundamental role of claudin-19 for normal renal tubular function and undisturbed organization and development of the retina. 17033971 2006