RXRG
retinoid X receptor gamma
Summary
This gene encodes a member of the retinoid X receptor (RXR) family of nuclear receptors which are involved in mediating the antiproliferative effects of retinoic acid (RA). This receptor forms dimers with the retinoic acid, thyroid hormone, and vitamin D receptors, increasing both DNA binding and transcriptional function on their respective response elements. This gene is expressed at significantly lower levels in non-small cell lung cancer cells. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jun 2010]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10918169 | 1:165,370,475 | G/C | 3 prime UTR variant | — |
| rs1306538888 | 1:165,370,534 | A/G | — | uncertain significance |
| rs283696 | 1:165,376,043 | T/C | splice region variant | — |
| rs776927068 | 1:165,376,064 | G/T | — | uncertain significance |
| rs773507609 | 1:165,376,109 | T/C | — | uncertain significance |
| rs1478125488 | 1:165,377,467 | G/T | — | uncertain significance |
| rs2134095 | 1:165,377,552 | G/C | synonymous variant | — |
| rs1416940954 | 1:165,380,011 | C/T | — | uncertain significance |
| rs757312135 | 1:165,380,267 | C/T | — | uncertain significance |
| rs199977692 | 1:165,380,286 | G/C | — | likely benign |
| rs759787868 | 1:165,380,319 | C/T | — | uncertain significance |
| rs2651860 | 1:165,381,055 | A/C | intron variant | — |
| rs1128977 | 1:165,389,129 | G/A | synonymous variant | — |
| rs2525076704 | 1:165,389,146 | C/A | — | uncertain significance |
| rs200646455 | 1:165,389,155 | C/T | — | uncertain significance |
| rs2525076968 | 1:165,389,194 | G/T | — | uncertain significance |
| rs2525076992 | 1:165,389,200 | C/G | — | uncertain significance |
| rs571691252 | 1:165,389,203 | G/T | — | uncertain significance |
| rs466639 | 1:165,394,882 | T/C | intron variant | — |
| rs1469851984 | 1:165,398,042 | G/C | — | uncertain significance |
| rs149455886 | 1:165,398,071 | G/T | — | uncertain significance |
| rs1394273977 | 1:165,398,083 | C/T | — | uncertain significance |
| rs113471 | 1:165,398,115 | T/C | synonymous variant | — |
| rs1278232099 | 1:165,398,154 | C/A | — | uncertain significance |
| rs371155454 | 1:165,398,162 | C/T | — | uncertain significance |
| rs285480 | 1:165,403,903 | G/T | — | — |
| rs10800098 | 1:165,409,095 | G/A | intron variant | — |
| rs2194899 | 1:165,410,785 | A/G | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.