MAGEA10


Description

The MAGEA10 (MAGE family member A10) is a protein-coding gene located on chromosome X.

MAGEA10, a protein-coding gene in humans, belongs to the MAGEA gene family located on the X chromosome at position Xq28. These genes share a high degree of sequence similarity and are thought to be involved in different transcriptional controls. MAGEA genes have been associated with disorders such as dyskeratosis congenita. Alternative splicing creates multiple transcript variants, and read-through transcription can occur between MAGEA10 and the MAGEA5 gene.

MAGEA10 is also known as CT1.10, MAGE10.

Associated Diseases



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