Gene: AGXT ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 189
Gene Symbol: AGXT
AGXT 		0.110 GeneticVariation disease CLINVAR Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis. 28893421 2018
Entrez Id: 189
Gene Symbol: AGXT
AGXT 		0.110 GeneticVariation disease BEFREE In this study, AGXT gene sequence analyses were performed in 82 patients who were clinically suspected (hyperoxaluria and nephrolithiasis or nephrocalcinosis with or without renal impairment) to have PH1. 27915025 2016
Entrez Id: 189
Gene Symbol: AGXT
AGXT 		0.110 Biomarker disease HPO