Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 81614
Gene Symbol: NIPA2
NIPA2
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		0.030 GeneticVariation BEFREE To reveal the pathogenesis and find the precision treatment for the childhood absence epilepsy (CAE) patients with NIPA2 mutations. 30895737

2019
Entrez Id: 81614
Gene Symbol: NIPA2
NIPA2
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		0.030 Biomarker BEFREE This study primarily reveals that a selective magnesium transporter NIPA2 may play a role in the pathogenesis of CAE. 25347071

2014
Entrez Id: 81614
Gene Symbol: NIPA2
NIPA2
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		0.030 Biomarker BEFREE We first identified that NIPA2, encoding a selective magnesium transporter, is a susceptible gene of CAE, and 15q11.2 microdeletions are important pathogenic CNVs for CAE with higher frequency in Chinese populations than that previously reported in Caucasians. 22367439

2012