Version 5.4
| Homo sapiens Gene: MAGEA3 | |||||||||||||||||||
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| Summary | |||||||||||||||||||
| InnateDB Gene | IDBG-281680.5 | ||||||||||||||||||
| Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
| Gene Symbol | MAGEA3 | ||||||||||||||||||
| Gene Name | melanoma antigen family A, 3 | ||||||||||||||||||
| Synonyms | CT1.3; HIP8; HYPD; MAGE3; MAGEA6 | ||||||||||||||||||
| Species | Homo sapiens | ||||||||||||||||||
| Ensembl Gene | ENSG00000221867 | ||||||||||||||||||
| Encoded Proteins |
melanoma antigen family A, 3
melanoma antigen family A, 3
melanoma antigen family A, 3
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| Protein Structure |
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| Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||||||
| Entrez Gene | |||||||||||||||||||
| 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. [provided by RefSeq, Jul 2008] 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] |
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| Gene Information | |||||||||||||||||||
| Type | Protein coding | ||||||||||||||||||
| Genomic Location | Chromosome X:152698752-152702347 | ||||||||||||||||||
| Strand | Forward strand | ||||||||||||||||||
| Band | q28 | ||||||||||||||||||
| Transcripts |
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| Interactions | |||||||||||||||||||
| Number of Interactions |
This gene and/or its encoded proteins are associated with 7 experimentally validated interaction(s) in this database.
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| Gene Ontology | |||||||||||||||||||
Molecular Function |
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| Biological Process |
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| Cellular Component |
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| Orthologs | |||||||||||||||||||
| No orthologs found for this gene | |||||||||||||||||||
| Cross-References | |||||||||||||||||||
| SwissProt | P43357 | ||||||||||||||||||
| TrEMBL | B9A060 E7EMU0 | ||||||||||||||||||
| UniProt Splice Variant | |||||||||||||||||||
| Entrez Gene | 4102 | ||||||||||||||||||
| UniGene | Hs.417816 Hs.441113 | ||||||||||||||||||
| RefSeq | NM_005362 XM_006724818 XM_005274676 | ||||||||||||||||||
| HUGO | HGNC:6801 | ||||||||||||||||||
| OMIM | 300174 | ||||||||||||||||||
| CCDS | CCDS76045 | ||||||||||||||||||
| HPRD | 02166 | ||||||||||||||||||
| IMGT | |||||||||||||||||||
| EMBL | AF002997 AK292384 BC000340 BC005963 BC011744 BC016803 BC017389 CR541767 CR541774 U03735 U82671 | ||||||||||||||||||
| GenPept | AAA17446 AAH00340 AAH05963 AAH11744 AAH16803 AAH17389 BAF85073 CAG46566 CAG46573 | ||||||||||||||||||
| RNA Seq Atlas | 4102 | ||||||||||||||||||