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 		0.110 GeneticVariation disease CLINVAR Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis. 28893421 2018
Entrez Id: 149461
Gene Symbol: CLDN19
CLDN19 		0.110 GeneticVariation disease BEFREE Alterations to claudins expressed in the TAL tight junction greatly affects calcium homeostasis as highlighted by point mutations in claudin-16 or claudin-19 causing FHHNC or gain of function mutations in claudin-14 causing kidney stones. 29782346 2018
Entrez Id: 149461
Gene Symbol: CLDN19
CLDN19 		0.110 Biomarker disease HPO