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: 441933
MIM: 611677
HGNC: 14999
Ensembl: ENSG00000197437
Variants:
dbSNP: 441933
ClinVar: 441933
TCGA: ENSG00000197437
COSMIC: OR13G1
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000197437 | ENST00000359688 | Q8NGZ3 |
| ENSG00000197437 | ENST00000642119 | Q8NGZ3 |
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 19709766 | 2011 | Variations of specific non-candidate genes and risk of myocardial infarction: a replication study. | 7 |
| 19709766 | 2011 | Variations of specific non-candidate genes and risk of myocardial infarction: a replication study. | 7 |
| 19023099 | 2009 | Gene variants associated with ischemic stroke: the cardiovascular health study. | 20 |
| 19056482 | 2009 | Association of a polymorphism of the apolipoprotein E gene with chronic kidney disease in Japanese individuals with metabolic syndrome. | 6 |
| 19166692 | 2009 | Usefulness of genetic polymorphisms and conventional risk factors to predict coronary heart disease in patients with familial hypercholesterolemia. | 14 |
| 19023099 | 2009 | Gene variants associated with ischemic stroke: the cardiovascular health study. | 20 |
| 19056482 | 2009 | Association of a polymorphism of the apolipoprotein E gene with chronic kidney disease in Japanese individuals with metabolic syndrome. | 6 |
| 19166692 | 2009 | Usefulness of genetic polymorphisms and conventional risk factors to predict coronary heart disease in patients with familial hypercholesterolemia. | 14 |
| 17975119 | 2008 | Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study. | 77 |
| 18599554 | 2008 | Replication study of 10 genetic polymorphisms associated with coronary heart disease in a specific high-risk population with familial hypercholesterolemia. | 18 |
| 17975119 | 2008 | Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study. | 77 |
| 18599554 | 2008 | Replication study of 10 genetic polymorphisms associated with coronary heart disease in a specific high-risk population with familial hypercholesterolemia. | 18 |
| 16175505 | 2005 | Identification of four gene variants associated with myocardial infarction. | 50 |
| 16175505 | 2005 | Identification of four gene variants associated with myocardial infarction. | 50 |
Citation
Dessen P
OR13G1 (olfactory receptor family 13 subfamily G member 1)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/71194/tumors-explorer/new-content/
