OR51B5
olfactory receptor family 51 subfamily B member 5
Summary
Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs551800558 | 11:5,362,354 | C/T | coding sequence variant | — |
| rs773359755 | 11:5,363,851 | G/C | — | uncertain significance |
| rs757159468 | 11:5,363,926 | C/T | — | uncertain significance |
| rs771089918 | 11:5,363,994 | A/G | — | uncertain significance |
| rs1848918438 | 11:5,364,048 | A/G | — | uncertain significance |
| rs371637413 | 11:5,364,075 | G/A | — | uncertain significance |
| rs763132943 | 11:5,364,150 | A/G | — | uncertain significance |
| rs771737118 | 11:5,364,199 | C/T | — | uncertain significance |
| rs767661897 | 11:5,364,253 | G/A | — | uncertain significance |
| rs201073099 | 11:5,364,277 | G/A | — | uncertain significance |
| rs148591287 | 11:5,364,321 | C/G | — | uncertain significance |
| rs767734992 | 11:5,364,339 | A/C | — | uncertain significance |
| rs547271833 | 11:5,364,342 | C/T | — | uncertain significance |
| rs1250585720 | 11:5,364,358 | C/T | — | likely benign |
| rs1848928074 | 11:5,364,405 | G/A | — | uncertain significance |
| rs1589942099 | 11:5,364,423 | C/G | — | uncertain significance |
| rs1435926857 | 11:5,364,438 | G/C | — | uncertain significance |
| rs1286534067 | 11:5,364,454 | A/G | — | uncertain significance |
| rs61738484 | 11:5,364,471 | C/A | — | uncertain significance |
| rs370740392 | 11:5,364,528 | A/G | — | uncertain significance |
| rs747190967 | 11:5,364,529 | T/C | — | uncertain significance |
| rs2494419095 | 11:5,364,541 | C/A | — | uncertain significance |
| rs546965603 | 11:5,364,551 | G/C | — | uncertain significance |
| rs763376441 | 11:5,364,552 | T/C | — | uncertain significance |
| rs5006884 | 11:5,373,251 | C/T | missense variant | — |
| rs535388418 | 11:5,376,172 | G/A | coding sequence variant | — |
| rs542968504 | 11:5,377,965 | G/A | — | — |
| rs149728699 | 11:5,385,204 | G/A | regulatory region variant | — |
| rs6578627 | 11:5,407,017 | C/T | upstream gene variant | — |
| rs770182365 | 11:5,429,769 | A/G | — | — |
| rs10838094 | 11:5,443,893 | G/C | missense variant | — |
| rs551956132 | 11:5,464,316 | A/C | — | — |
| rs10500641 | 11:5,469,576 | C/T | intron variant | — |
| rs7948471 | 11:5,471,746 | G/A | upstream gene variant | — |
| rs11037480 | 11:5,472,472 | T/C | upstream gene variant | — |
| rs547614934 | 11:5,507,182 | C/T | — | — |
| rs73392143 | 11:5,513,654 | G/T | downstream gene variant | — |
| rs372091 | 11:5,518,156 | A/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.