Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2677
Gene Symbol: GGCX
GGCX 		0.500 Biomarker disease RGD Enhanced renal vitamin-K-dependent gamma-glutamyl carboxylase activity in experimental rat urolithiasis. 9471053 1998
Entrez Id: 2677
Gene Symbol: GGCX
GGCX 		0.500 Biomarker disease CTD_human Enhanced renal vitamin-K-dependent gamma-glutamyl carboxylase activity in experimental rat urolithiasis. 9471053 1998
Entrez Id: 353
Gene Symbol: APRT
APRT 		0.330 Biomarker disease BEFREE Appropriate treatment should be initiated to prevent the development of urolithiasis or renal failure in APRT-deficient children. 21635362 2011
Entrez Id: 353
Gene Symbol: APRT
APRT 		0.330 GeneticVariation disease BEFREE Adenine phosphoribosyltransferase (APRT) deficiency leading to 2,8-dihydroxyadenine (DHA) urolithiasis has been considered a rare cause of urolithiasis and renal insufficiency. 3817810 1987
Entrez Id: 353
Gene Symbol: APRT
APRT 		0.330 GeneticVariation disease BEFREE In the present investigations, we have shown that this characteristic is common in mutant enzymes from all the four separate Japanese urolithiasis families associated with partial APRT deficiencies so far tested. 3876264 1985
Entrez Id: 353
Gene Symbol: APRT
APRT 		0.330 Biomarker disease CTD_human In the present investigations, we have shown that this characteristic is common in mutant enzymes from all the four separate Japanese urolithiasis families associated with partial APRT deficiencies so far tested. 3876264 1985
Entrez Id: 353
Gene Symbol: APRT
APRT 		0.330 Biomarker disease CTD_human Child's urinary lithiasis revealing a complete deficit in adenine phosphoribosyl transferase. 7766 1976
Entrez Id: 10861
Gene Symbol: SLC26A1
SLC26A1 		0.300 Biomarker disease CTD_human Urolithiasis and hepatotoxicity are linked to the anion transporter Sat1 in mice. 20160351 2010
Entrez Id: 10861
Gene Symbol: SLC26A1
SLC26A1 		0.300 Biomarker disease CTD_human Oxalate is then excreted by the kidneys via the basolateral sat-1 (males > females) and the apical CFEX (Slc26a6; GD unknown) in PT and eliminated in the urine (males > females), where it may contribute to the male-prevailing development of oxalate urolithiasis. 19002488 2009
Entrez Id: 23562
Gene Symbol: CLDN14
CLDN14 		0.110 GeneticVariation disease GWASCAT Novel Risk Loci Identified in a Genome-Wide Association Study of Urolithiasis in a Japanese Population. 30975718 2019
Entrez Id: 23562
Gene Symbol: CLDN14
CLDN14 		0.110 Biomarker disease BEFREE Genome-wide association studies have shown that CLDN14 and NPT2 are associated with urolithiasis in Caucasian and Japanese populations, respectively. 27539983 2017
Entrez Id: 5585
Gene Symbol: PKN1
PKN1 		0.100 GeneticVariation disease GWASCAT Novel Risk Loci Identified in a Genome-Wide Association Study of Urolithiasis in a Japanese Population. 30975718 2019
Entrez Id: 7421
Gene Symbol: VDR
VDR 		0.100 GeneticVariation disease BEFREE No associations were evident for VDR ApaI, BsmI and TaqI polymorphic variants and urolithiasis risk after correction for multiple testing. 31515573 2019
Entrez Id: 7421
Gene Symbol: VDR
VDR 		0.100 GeneticVariation disease BEFREE The keywords used for the search were "vitamin D receptor or VDR" and "polymorphisms or SNPs" combined with "urolithiasis or nephrolithiasis". 31212049 2019
Entrez Id: 7421
Gene Symbol: VDR
VDR 		0.100 GeneticVariation disease BEFREE In our population, CO2CP and levels of uric acid and serum Na as well as polymorphism of the F allele of the VDR FokⅠ may provide important clues to evaluate the risk of urolithiasis in Uyghur children. 30742686 2019
Entrez Id: 7021
Gene Symbol: TFAP2B
TFAP2B 		0.100 GeneticVariation disease GWASCAT Novel Risk Loci Identified in a Genome-Wide Association Study of Urolithiasis in a Japanese Population. 30975718 2019
Entrez Id: 10636
Gene Symbol: RGS14
RGS14 		0.100 GeneticVariation disease GWASCAT Novel Risk Loci Identified in a Genome-Wide Association Study of Urolithiasis in a Japanese Population. 30975718 2019
Entrez Id: 54828
Gene Symbol: BCAS3
BCAS3 		0.100 GeneticVariation disease GWASCAT Novel Risk Loci Identified in a Genome-Wide Association Study of Urolithiasis in a Japanese Population. 30975718 2019
Entrez Id: 2037
Gene Symbol: EPB41L2
EPB41L2 		0.100 GeneticVariation disease GWASCAT Novel Risk Loci Identified in a Genome-Wide Association Study of Urolithiasis in a Japanese Population. 30975718 2019
Entrez Id: 79068
Gene Symbol: FTO
FTO 		0.100 GeneticVariation disease GWASCAT Novel Risk Loci Identified in a Genome-Wide Association Study of Urolithiasis in a Japanese Population. 30975718 2019
Entrez Id: 160851
Gene Symbol: DGKH
DGKH 		0.100 GeneticVariation disease GWASCAT Novel Risk Loci Identified in a Genome-Wide Association Study of Urolithiasis in a Japanese Population. 30975718 2019
Entrez Id: 84182
Gene Symbol: MINDY4
MINDY4 		0.100 GeneticVariation disease GWASCAT Novel Risk Loci Identified in a Genome-Wide Association Study of Urolithiasis in a Japanese Population. 30975718 2019
Entrez Id: 2646
Gene Symbol: GCKR
GCKR 		0.100 GeneticVariation disease GWASCAT Novel Risk Loci Identified in a Genome-Wide Association Study of Urolithiasis in a Japanese Population. 30975718 2019
Entrez Id: 204474
Gene Symbol: PDILT
PDILT 		0.100 GeneticVariation disease GWASCAT Novel Risk Loci Identified in a Genome-Wide Association Study of Urolithiasis in a Japanese Population. 30975718 2019
Entrez Id: 100526825
Gene Symbol: INMT-MINDY4
INMT-MINDY4 		0.100 GeneticVariation disease GWASCAT Novel Risk Loci Identified in a Genome-Wide Association Study of Urolithiasis in a Japanese Population. 30975718 2019