Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 57692
MIM: 300759
HGNC: 24934
Ensembl: ENSG00000198934
Variants:
dbSNP: 57692
ClinVar: 57692
TCGA: ENSG00000198934
COSMIC: MAGEE1
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000198934 | ENST00000361470 | Q9HCI5 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 23268337 | 2013 | Naturally occurring HCA1 missense mutations result in loss of function: potential impact on lipid deposition. | 3 |
| 23268337 | 2013 | Naturally occurring HCA1 missense mutations result in loss of function: potential impact on lipid deposition. | 3 |
| 20862285 | 2010 | Frequent MAGE mutations in human melanoma. | 16 |
| 20862285 | 2010 | Frequent MAGE mutations in human melanoma. | 16 |
| 14623885 | 2004 | DAMAGE, a novel alpha-dystrobrevin-associated MAGE protein in dystrophin complexes. | 12 |
| 14623885 | 2004 | DAMAGE, a novel alpha-dystrobrevin-associated MAGE protein in dystrophin complexes. | 12 |
Citation
Dessen P
MAGEE1 (MAGE family member E1)
Atlas Genet Cytogenet Oncol Haematol. 2003-06-01
Online version: http://atlasgeneticsoncology.org/gene/41066/magee1
