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MAGED2, MAGE family member D2

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MAGED2, MAGE family member D2

  • This gene is a member of the MAGED gene family. The MAGED genes are clustered on chromosome Xp11. This gene is located in Xp11.2, a hot spot for X-linked intellectual disability (XLID). Mutations in this gene cause a form of transient antenatal Bartter's syndrome. This gene may also be involved in several types of cancer, including breast cancer and melanoma. The protein encoded by this gene is progressively recruited from the cytoplasm to the nucleoplasm during the interphase and after nucleolar stress and is thus thought to play a role in cell cycle regulation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2017]

  • Gene Synonyms (11B6, BARTS5, BCG-1, BCG1, HCA10, MAGE-D2, melanoma-associated antigen D2, MAGE-D2 antigen, breast cancer-associated gene 1 protein, hepatocellular carcinoma-associated protein JCL-1, melanoma antigen family D, 2, melanoma antigen family D2,)
  • NCBI Gene ID: 10916
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q9UNF1
    UNIPROT ID#>>A0A024R9Y7
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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

MAGE family member D2 interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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