MAGT1, magnesium transporter 1

MAGT1, magnesium transporter 1

• This gene encodes a ubiquitously expressed magnesium cation transporter protein that localizes to the cell membrane. This protein also associates with N-oligosaccharyl transferase and therefore may have a role in N-glycosylation. Mutations in this gene cause a form of X-linked intellectual disability (XLID). This gene may have multiple in-frame translation initiation sites, one of which would encode a shorter protein with an N-terminus containing a signal peptide at amino acids 1-29. [provided by RefSeq, Jul 2017]

• Gene Synonyms (magnesium transporter protein 1, dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit MAGT1, implantation-associated protein, oligosaccharyl transferase subunit MAGT1, oligosaccharyltransferase 3 homolog B, CDG1CC, IAP, MRX95, OST3B, PRO0756, SLC58A1, XMEN, bA217H1.1,)
• NCBI Gene ID: 84061
• Species: Homo sapiens (Human)
• UNIPROT ID#>>A0A087WU53
  UNIPROT ID#>>Q9H0U3
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

magnesium transporter 1 interacts with:

• calreticulin 3
  EvC ciliary complex subunit 2
  kinesin family member 19A
  lactate dehydrogenase D
  leucine rich repeat kinase 2
  NEDD1 gamma-tubulin ring complex targeting factor
  ring finger protein 157
  STT3 oligosaccharyltransferase complex catalytic subunit B
  translocase of outer mitochondrial membrane 5
  transmembrane protein 67
  yippee like 5

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.