RMDN2
regulator of microtubule dynamics 2
Summary
Enables microtubule binding activity. Located in Golgi apparatus; cytosol; and spindle. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1049449941 | 2:38,156,431 | C/A | — | uncertain significance |
| rs567727832 | 2:38,156,498 | G/C | — | uncertain significance |
| rs2466128009 | 2:38,156,531 | G/A | — | uncertain significance |
| rs750621679 | 2:38,156,764 | T/A | — | uncertain significance |
| rs182370326 | 2:38,164,013 | T/C | intron variant | — |
| rs1188707586 | 2:38,178,392 | C/G | — | uncertain significance |
| rs146510382 | 2:38,178,411 | C/T | — | uncertain significance |
| rs141147110 | 2:38,178,446 | C/T | — | uncertain significance |
| rs773070126 | 2:38,178,459 | C/T | — | uncertain significance |
| rs752203212 | 2:38,178,515 | C/A | — | uncertain significance |
| rs750918733 | 2:38,178,528 | C/A | — | uncertain significance |
| rs1324824276 | 2:38,178,574 | C/G | — | uncertain significance |
| rs370260752 | 2:38,178,684 | A/G | — | uncertain significance |
| rs1051283312 | 2:38,178,744 | C/G | — | uncertain significance |
| rs777954963 | 2:38,178,756 | G/A | — | uncertain significance |
| rs769302943 | 2:38,178,807 | G/A | — | uncertain significance |
| rs1183897649 | 2:38,178,818 | T/C | — | uncertain significance |
| rs768531525 | 2:38,178,857 | A/G | — | uncertain significance |
| rs75699143 | 2:38,178,877 | A/G | — | benign |
| rs372732058 | 2:38,178,937 | C/G | — | likely benign |
| rs200577012 | 2:38,178,969 | A/T | — | uncertain significance |
| rs1205703330 | 2:38,179,044 | A/G | — | uncertain significance |
| rs116259556 | 2:38,179,072 | G/A | — | benign |
| rs368297189 | 2:38,179,127 | A/G | — | uncertain significance |
| rs148437492 | 2:38,179,145 | A/G | — | uncertain significance |
| rs145168314 | 2:38,179,164 | C/G | — | uncertain significance |
| rs573063895 | 2:38,179,167 | C/G | — | uncertain significance |
| rs1356254708 | 2:38,179,240 | C/G | — | uncertain significance |
| rs374259749 | 2:38,179,244 | C/T | — | likely benign |
| rs2466346319 | 2:38,179,260 | C/T | — | uncertain significance |
| rs1381121096 | 2:38,179,292 | G/C | — | uncertain significance |
| rs200724936 | 2:38,179,330 | A/C | — | uncertain significance |
| rs138851338 | 2:38,201,247 | C/T | — | uncertain significance |
| rs2466684256 | 2:38,201,286 | G/C | — | uncertain significance |
| rs201237503 | 2:38,201,340 | C/T | — | likely benign |
| rs201685599 | 2:38,201,345 | C/A | — | uncertain significance |
| rs369570141 | 2:38,202,424 | A/G | — | likely benign |
| rs781065769 | 2:38,208,456 | G/C | — | uncertain significance |
| rs1016272455 | 2:38,216,704 | A/G | — | uncertain significance |
| rs1023186607 | 2:38,216,738 | C/G | — | uncertain significance |
| rs150686656 | 2:38,218,372 | G/A | — | uncertain significance |
| rs753770630 | 2:38,218,402 | C/G | — | uncertain significance |
| rs776173419 | 2:38,218,428 | A/C | — | uncertain significance |
| rs2465400298 | 2:38,218,433 | G/T | — | uncertain significance |
| rs773515557 | 2:38,224,638 | C/G | — | uncertain significance |
| rs368925051 | 2:38,224,643 | C/T | — | uncertain significance |
| rs1218464343 | 2:38,224,651 | C/G | — | uncertain significance |
| rs145720933 | 2:38,231,345 | A/G | — | uncertain significance |
| rs6741148 | 2:38,277,832 | T/C | — | — |
| rs13417487 | 2:38,289,162 | G/T | downstream gene variant | — |
| rs11674584 | 2:38,290,743 | T/C | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.