RecName: Full=Magnesium transporter protein 1; Short=MagT1; AltName: F - Protein

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HLH and Recurrent EBV Lymphoma as the presenting manifestation of MAGT1 Deficiency: A Systematic Review of the Expanding Disease Spectrum. [J Clin Immunol. 2024]
HLH and Recurrent EBV Lymphoma as the presenting manifestation of MAGT1 Deficiency: A Systematic Review of the Expanding Disease Spectrum.
Golloshi K, Mitchell W, Kumar D, Malik S, Parikh S, Aljudi AA, Castellino SM, Chandrakasan S. J Clin Immunol. 2024 Jun 19; 44(7):153. Epub 2024 Jun 19.
Identification of a novel MAGT1 mutation supports a diagnosis of XMEN disease. [Genes Immun. 2022]
Identification of a novel MAGT1 mutation supports a diagnosis of XMEN disease.
Watson CM, Nadat F, Ahmed S, Crinnion LA, O'Riordan S, Carter C, Savic S. Genes Immun. 2022 Apr; 23(2):66-72. Epub 2022 Mar 9.
Lack of NKG2D in MAGT1-deficient patients is caused by hypoglycosylation. [Hum Genet. 2022]
Lack of NKG2D in MAGT1-deficient patients is caused by hypoglycosylation.
Blommaert E, Cherepanova NA, Staels F, Wilson MP, Gilmore R, Schrijvers R, Jaeken J, Foulquier F, Matthijs G. Hum Genet. 2022 Jul; 141(7):1279-1286. Epub 2022 Feb 19.

RefSeq genomic sequence
See the genomic reference sequence for the MAGT1 gene (NG_016390.1).
RefSeq protein isoforms
See 2 reference sequence protein isoforms for the MAGT1 gene.

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Q9H0U3 [Domain Mapping of Disease Mut...]
Q9H0U3
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
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RecName: Full=Magnesium transporter protein 1; Short=MagT1; AltName: Full=Dolich...
RecName: Full=Magnesium transporter protein 1; Short=MagT1; AltName: Full=Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit MAGT1; Short=Oligosaccharyl transferase subunit MAGT1; AltName: Full=Implantation-associated protein; Short=IAP; Flags: Precursor
gi|74761391|sp|Q9H0U3.1|MAGT1_HUMAN

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