RTN4R
reticulon 4 receptor
Summary
This gene encodes the receptor for reticulon 4, oligodendrocyte myelin glycoprotein and myelin-associated glycoprotein. This receptor mediates axonal growth inhibition and may play a role in regulating axonal regeneration and plasticity in the adult central nervous system. [provided by RefSeq, Jul 2008]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs701428 | 22:20,228,542 | A/T | — | — |
| rs962899274 | 22:20,229,248 | G/A | — | uncertain significance |
| rs1309033080 | 22:20,229,258 | C/T | — | likely benign |
| rs1408533262 | 22:20,229,263 | C/T | — | uncertain significance |
| rs994098884 | 22:20,229,280 | G/C | — | uncertain significance |
| rs1478373174 | 22:20,229,283 | G/A | — | uncertain significance |
| rs374126911 | 22:20,229,291 | G/A | — | likely benign |
| rs368329252 | 22:20,229,338 | C/T | — | uncertain significance |
| rs113649687 | 22:20,229,355 | G/T | — | uncertain significance |
| rs1296361027 | 22:20,229,357 | C/G | — | uncertain significance |
| rs749760894 | 22:20,229,449 | A/G | — | uncertain significance |
| rs754570266 | 22:20,229,517 | T/C | — | uncertain significance |
| rs779384862 | 22:20,229,526 | C/T | — | uncertain significance |
| rs760190468 | 22:20,229,539 | C/T | — | uncertain significance |
| rs144464748 | 22:20,229,540 | G/A | — | likely benign |
| rs149231717 | 22:20,229,569 | C/T | — | likely benign |
| rs145150796 | 22:20,229,570 | G/A | — | likely benign |
| rs138981042 | 22:20,229,590 | C/T | — | uncertain significance |
| rs762415688 | 22:20,229,724 | A/G | — | uncertain significance |
| rs369655638 | 22:20,229,751 | G/C | — | uncertain significance |
| rs374205280 | 22:20,229,769 | C/T | — | uncertain significance |
| rs377689400 | 22:20,229,805 | T/A | — | uncertain significance |
| rs144550064 | 22:20,229,820 | C/T | — | uncertain significance |
| rs2517284853 | 22:20,229,847 | G/T | — | uncertain significance |
| rs777345223 | 22:20,230,000 | G/A | — | uncertain significance |
| rs147591609 | 22:20,230,067 | C/T | — | uncertain significance |
| rs74315509 | 22:20,230,069 | C/T | missense variant | risk factor |
| rs746384572 | 22:20,230,091 | G/A | — | uncertain significance |
| rs770160195 | 22:20,230,097 | C/T | — | uncertain significance |
| rs1464355538 | 22:20,230,100 | G/A | — | uncertain significance |
| rs1370988148 | 22:20,230,128 | G/A | — | likely benign |
| rs117955118 | 22:20,230,140 | G/C | — | uncertain significance |
| rs113041746 | 22:20,230,216 | G/A | — | uncertain significance |
| rs775504686 | 22:20,230,240 | C/T | — | uncertain significance |
| rs780355528 | 22:20,230,274 | C/G | — | uncertain significance |
| rs74315508 | 22:20,230,301 | G/A | missense variant | risk factor |
| rs149052299 | 22:20,230,317 | G/A | — | likely benign |
| rs745997652 | 22:20,230,414 | C/T | — | uncertain significance |
| rs539553864 | 22:20,230,415 | G/A | — | uncertain significance |
| rs774499670 | 22:20,230,423 | C/T | — | likely benign |
| rs2517285495 | 22:20,230,444 | T/A | — | uncertain significance |
| rs369027983 | 22:20,230,562 | C/T | — | uncertain significance |
| rs1365079965 | 22:20,230,628 | G/A | — | uncertain significance |
| rs701427 | 22:20,233,268 | A/G | — | — |
| rs854971 | 22:20,233,429 | T/C | downstream gene variant | — |
| rs887765 | 22:20,234,817 | C/T | regulatory region variant | — |
| rs696880 | 22:20,235,200 | G/A | regulatory region variant | — |
| rs1567871 | 22:20,241,160 | C/T | upstream gene variant | — |
| rs701421 | 22:20,246,081 | T/C | — | — |
| rs146835471 | 22:20,256,670 | G/A | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.