OR13G1 (olfactory receptor family 13 subfamily G member 1)

2014-11-01  

Identity

HGNC
LOCATION
1q44
LOCUSID
ALIAS
OR1-37

Other Information

Locus ID:

NCBI: 441933
MIM: 611677
HGNC: 14999
Ensembl: ENSG00000197437

Variants:

dbSNP: 441933
ClinVar: 441933
TCGA: ENSG00000197437
COSMIC: OR13G1

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000197437ENST00000359688Q8NGZ3
ENSG00000197437ENST00000642119Q8NGZ3

Expression (GTEx)

0
1

Pathways

PathwaySourceExternal ID
Olfactory transductionKEGGko04740
Olfactory transductionKEGGhsa04740
Signal TransductionREACTOMER-HSA-162582
Signaling by GPCRREACTOMER-HSA-372790
GPCR downstream signalingREACTOMER-HSA-388396
Olfactory Signaling PathwayREACTOMER-HSA-381753

References

Pubmed IDYearTitleCitations
197097662011Variations of specific non-candidate genes and risk of myocardial infarction: a replication study.7
197097662011Variations of specific non-candidate genes and risk of myocardial infarction: a replication study.7
190230992009Gene variants associated with ischemic stroke: the cardiovascular health study.20
190564822009Association of a polymorphism of the apolipoprotein E gene with chronic kidney disease in Japanese individuals with metabolic syndrome.6
191666922009Usefulness of genetic polymorphisms and conventional risk factors to predict coronary heart disease in patients with familial hypercholesterolemia.14
190230992009Gene variants associated with ischemic stroke: the cardiovascular health study.20
190564822009Association of a polymorphism of the apolipoprotein E gene with chronic kidney disease in Japanese individuals with metabolic syndrome.6
191666922009Usefulness of genetic polymorphisms and conventional risk factors to predict coronary heart disease in patients with familial hypercholesterolemia.14
179751192008Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study.77
185995542008Replication study of 10 genetic polymorphisms associated with coronary heart disease in a specific high-risk population with familial hypercholesterolemia.18
179751192008Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study.77
185995542008Replication study of 10 genetic polymorphisms associated with coronary heart disease in a specific high-risk population with familial hypercholesterolemia.18
161755052005Identification of four gene variants associated with myocardial infarction.50
161755052005Identification 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/or13g1-(olfactory-receptor-family-13-subfamily-g-member-1)