MAGEA10 - MAGE family member A10 Gene
Also Known as CT1.10; MAGE10
Species: Homo sapiens
About MAGEA10
This gene has 6 transcripts (splice variants), 208 orthologues and 37 paralogues. Biased expression in placenta (RPKM 4.9) and testis (RPKM 1.2).
Summary
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. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream melanoma antigen family A, 5 (MAGEA5) gene.[provided by RefSeq, Oct 2011]
MAGEA10 Products (3)
| mRNA | Protein | Name |
|---|---|---|
| NM_001011543.3 | NP_001011543.3 | melanoma-associated antigen 10 |
| NM_001251828.2 | NP_001238757.2 | melanoma-associated antigen 10 |
| NM_021048.5 | NP_066386.3 | melanoma-associated antigen 10 |
MAGEA10 Protein Structure
MAGE_N: Melanoma associated antigen family N terminal (3 - 60)
MAGE_N: Melanoma associated antigen family N terminal (58 - 119)
MAGE: MAGE family (141 - 311)
- 0
- 100
- 200
- 300
- 369 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
melanoma-associated antigen 10 |
|
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Melanoma |
|
|
| Dyskeratosis Congenita |
|
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Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Rattus norvegicus | MAGEA10 | RGD | RGD:1563693 |
| Others | MAGEA10 | NCBI |