MON1A
MON1 vesicular trafficking associated A
Summary
Enables guanyl-nucleotide exchange factor activity. Predicted to be involved in protein secretion. Predicted to act upstream of or within establishment of localization in cell; intracellular iron ion homeostasis; and protein transport. Part of Mon1-Ccz1 complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs373133949 | 3:49,946,475 | A/T | — | uncertain significance |
| rs752527712 | 3:49,946,478 | C/T | — | uncertain significance |
| rs2082843549 | 3:49,946,502 | C/T | — | uncertain significance |
| rs199551254 | 3:49,946,527 | C/T | — | uncertain significance |
| rs200619339 | 3:49,946,577 | G/A | — | uncertain significance |
| rs762324470 | 3:49,946,705 | T/C | — | uncertain significance |
| rs765508531 | 3:49,946,825 | A/G | — | uncertain significance |
| rs751716934 | 3:49,947,636 | G/A | — | uncertain significance |
| rs370695036 | 3:49,947,639 | C/T | — | uncertain significance |
| rs377517287 | 3:49,947,640 | G/A | — | uncertain significance |
| rs199835897 | 3:49,947,765 | G/C | — | uncertain significance |
| rs753657449 | 3:49,947,784 | A/C | — | uncertain significance |
| rs779478155 | 3:49,947,819 | T/C | — | uncertain significance |
| rs963475088 | 3:49,947,843 | G/A | — | uncertain significance |
| rs199606970 | 3:49,947,954 | C/T | — | uncertain significance |
| rs201823530 | 3:49,949,019 | T/A | — | uncertain significance |
| rs2545377904 | 3:49,949,039 | A/G | — | uncertain significance |
| rs775910900 | 3:49,949,169 | G/A | — | uncertain significance |
| rs758490585 | 3:49,949,202 | G/A | — | uncertain significance |
| rs747943003 | 3:49,949,256 | G/A | — | uncertain significance |
| rs375068093 | 3:49,949,309 | C/G | — | uncertain significance |
| rs770345029 | 3:49,949,376 | C/T | — | uncertain significance |
| rs199559150 | 3:49,949,430 | C/T | — | uncertain significance |
| rs757855583 | 3:49,949,441 | G/A | — | uncertain significance |
| rs7634084 | 3:49,949,834 | A/T | intron variant | — |
| rs760700841 | 3:49,950,692 | C/G | — | uncertain significance |
| rs761732784 | 3:49,950,704 | T/A | — | uncertain significance |
| rs148483316 | 3:49,950,712 | C/A | — | uncertain significance |
| rs765908206 | 3:49,950,730 | G/A | — | uncertain significance |
| rs370877712 | 3:49,950,746 | C/T | — | uncertain significance |
| rs780195420 | 3:49,950,776 | C/T | — | uncertain significance |
| rs34034116 | 3:49,959,156 | C/A | downstream gene variant | — |
| rs62262093 | 3:49,960,388 | T/C | intron variant | — |
| rs35917071 | 3:49,965,609 | T/A | intron variant | — |
| rs373514881 | 3:49,967,059 | C/A | — | uncertain significance |
| rs2545401491 | 3:49,967,084 | A/G | — | uncertain significance |
| rs1180923360 | 3:49,967,166 | C/T | — | uncertain significance |
| rs943173689 | 3:49,967,203 | C/G | — | uncertain significance |
| rs2083079272 | 3:49,967,219 | T/A | — | uncertain significance |
| rs1348293646 | 3:49,967,228 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.