Identity
HGNC
LOCATION
Xp11.22
LOCUSID
ALIAS
DLXIN-1,NRAGE
FUSION GENES
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: 9500
MIM: 300224
HGNC: 6813
Ensembl: ENSG00000179222
Variants:
dbSNP: 9500
ClinVar: 9500
TCGA: ENSG00000179222
COSMIC: MAGED1
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000179222 | ENST00000326587 | Q9Y5V3 |
| ENSG00000179222 | ENST00000375695 | Q9Y5V3 |
| ENSG00000179222 | ENST00000375722 | Q9Y5V3 |
| ENSG00000179222 | ENST00000375772 | Q9Y5V3 |
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 31916845 | 2020 | Knockdown of NRAGE Impairs Homologous Recombination Repair and Sensitizes Hepatoblastoma Cells to Ionizing Radiation. | 3 |
| 31916845 | 2020 | Knockdown of NRAGE Impairs Homologous Recombination Repair and Sensitizes Hepatoblastoma Cells to Ionizing Radiation. | 3 |
| 29516958 | 2018 | The role of NRAGE subcellular location and epithelial-mesenchymal transition on radiation resistance of esophageal carcinoma cell. | 5 |
| 29778424 | 2018 | NRAGE confers poor prognosis and promotes proliferation, invasion, and chemoresistance in gastric cancer. | 5 |
| 30508943 | 2018 | NRAGE is a potential diagnostic biomarker of hepatocellular carcinoma. | 2 |
| 29516958 | 2018 | The role of NRAGE subcellular location and epithelial-mesenchymal transition on radiation resistance of esophageal carcinoma cell. | 5 |
| 29778424 | 2018 | NRAGE confers poor prognosis and promotes proliferation, invasion, and chemoresistance in gastric cancer. | 5 |
| 30508943 | 2018 | NRAGE is a potential diagnostic biomarker of hepatocellular carcinoma. | 2 |
| 28414775 | 2017 | Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability. | 7 |
| 28427939 | 2017 | NRAGE induces β-catenin/Arm O-GlcNAcylation and negatively regulates Wnt signaling. | 3 |
| 28639909 | 2017 | Silencing of NRAGE induces autophagy via AMPK/Ulk1/Atg13 signaling pathway in NSCLC cells. | 3 |
| 28414775 | 2017 | Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability. | 7 |
| 28427939 | 2017 | NRAGE induces β-catenin/Arm O-GlcNAcylation and negatively regulates Wnt signaling. | 3 |
| 28639909 | 2017 | Silencing of NRAGE induces autophagy via AMPK/Ulk1/Atg13 signaling pathway in NSCLC cells. | 3 |
| 26738870 | 2016 | Identification of novel NRAGE involved in the radioresistance of esophageal cancer cells. | 8 |
Citation
Dessen P
MAGED1 (MAGE family member D1)
Atlas Genet Cytogenet Oncol Haematol. 2003-06-01
Online version: http://atlasgeneticsoncology.org/gene/41261/maged1-(mage-family-member-d1)
