MAGT1, magnesium transporter 1, 84061

N. diseases: 120; N. variants: 8
Disease: Intellectual Disability ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.030 Biomarker group BEFREE On the other hand, recent genetic investigations question the previously proposed role for MAGT1 in intellectual disability. 26422833 2015
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.030 Biomarker group BEFREE MAGT1 is an Mg²⁺ transporter previously associated with primary immunodeficiency and ID, whereas mutations in ATRX cause ATRX-ID syndrome. 24130152 2014
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.030 GeneticVariation group LHGDN Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation. 18455129 2008