This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. [provided by RefSeq, Jul 2008]
Function:
Not known, though may play a role in embryonal development and tumor transformation or aspects of tumor progression.
Tissue Specificity:
Expressed in many tumors of several types, such as melanoma, head and neck squamous cell carcinoma, lung carcinoma and breast carcinoma, but not in normal tissues except for testes and placenta.
Similarity:
Contains 1 MAGE domain.
SWISS:
P43362
Gene ID:
4108
Database links:
Entrez Gene: 4108 Human
Entrez Gene: 728269 Human
Omim: 300342 Human
SwissProt: P43362 Human
Unigene: 92974 Human
Unigene: 512582 Human
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