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: 343171
MIM: 616729
HGNC: 15021
Ensembl: ENSG00000238243
Variants:
dbSNP: 343171
ClinVar: 343171
TCGA: ENSG00000238243
COSMIC: OR2W3
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000238243 | ENST00000360358 | Q7Z3T1 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 33097666 | 2020 | The odorant receptor OR2W3 on airway smooth muscle evokes bronchodilation via a cooperative chemosensory tradeoff between TMEM16A and CFTR. | 10 |
| 33097666 | 2020 | The odorant receptor OR2W3 on airway smooth muscle evokes bronchodilation via a cooperative chemosensory tradeoff between TMEM16A and CFTR. | 10 |
| 27916748 | 2017 | OR2M3: A Highly Specific and Narrowly Tuned Human Odorant Receptor for the Sensitive Detection of Onion Key Food Odorant 3-Mercapto-2-methylpentan-1-ol. | 23 |
| 28262088 | 2017 | Genome-Wide Association Study of Post-Traumatic Stress Disorder in Two High-Risk Populations. | 9 |
| 27916748 | 2017 | OR2M3: A Highly Specific and Narrowly Tuned Human Odorant Receptor for the Sensitive Detection of Onion Key Food Odorant 3-Mercapto-2-methylpentan-1-ol. | 23 |
| 28262088 | 2017 | Genome-Wide Association Study of Post-Traumatic Stress Disorder in Two High-Risk Populations. | 9 |
| 26891008 | 2016 | OR2W3 sequence variants are unlikely to cause inherited retinal diseases. | 4 |
| 26891008 | 2016 | OR2W3 sequence variants are unlikely to cause inherited retinal diseases. | 4 |
| 25374392 | 2015 | Association of single nucleotide polymorphisms in the USF1, GTF2A1L and OR2W3 genes with non-obstructive azoospermia in the Chinese population. | 2 |
| 25783483 | 2015 | Whole-exome sequencing identifies OR2W3 mutation as a cause of autosomal dominant retinitis pigmentosa. | 12 |
| 25847845 | 2015 | Susceptibility to male infertility: replication study in Japanese men looking for an association with four GWAS-derived loci identified in European men. | 0 |
| 25374392 | 2015 | Association of single nucleotide polymorphisms in the USF1, GTF2A1L and OR2W3 genes with non-obstructive azoospermia in the Chinese population. | 2 |
| 25783483 | 2015 | Whole-exome sequencing identifies OR2W3 mutation as a cause of autosomal dominant retinitis pigmentosa. | 12 |
| 25847845 | 2015 | Susceptibility to male infertility: replication study in Japanese men looking for an association with four GWAS-derived loci identified in European men. | 0 |
Citation
Dessen P
OR2W3 (olfactory receptor family 2 subfamily W member 3)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/71295/or2w3-(olfactory-receptor-family-2-subfamily-w-member-3)
