FIGN
fidgetin, microtubule severing factor
Summary
Predicted to enable ATP hydrolysis activity and microtubule severing ATPase activity. Predicted to be involved in cell division and microtubule cytoskeleton organization. Predicted to act upstream of or within locomotory behavior. Predicted to be located in nuclear matrix. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs202007179 | 2:164,466,172 | C/T | — | uncertain significance |
| rs1691190448 | 2:164,466,262 | C/T | — | uncertain significance |
| rs772366924 | 2:164,466,298 | C/T | — | uncertain significance |
| rs1691196308 | 2:164,466,409 | T/C | — | uncertain significance |
| rs1691197029 | 2:164,466,433 | C/T | — | uncertain significance |
| rs374396460 | 2:164,466,520 | C/T | — | uncertain significance |
| rs748183827 | 2:164,466,532 | G/A | — | uncertain significance |
| rs2467836882 | 2:164,466,560 | T/G | — | uncertain significance |
| rs201166518 | 2:164,466,673 | C/T | — | uncertain significance |
| rs1490839889 | 2:164,466,730 | A/G | — | uncertain significance |
| rs1268336530 | 2:164,466,736 | C/A | — | uncertain significance |
| rs762741451 | 2:164,466,788 | T/G | — | uncertain significance |
| rs759236740 | 2:164,466,868 | C/T | — | uncertain significance |
| rs1691214593 | 2:164,466,907 | G/T | — | uncertain significance |
| rs745997168 | 2:164,466,967 | C/T | — | uncertain significance |
| rs769689570 | 2:164,466,968 | G/T | — | uncertain significance |
| rs1156642059 | 2:164,467,080 | T/G | — | uncertain significance |
| rs1290259645 | 2:164,467,137 | G/A | — | uncertain significance |
| rs370402484 | 2:164,467,156 | T/C | — | uncertain significance |
| rs762970125 | 2:164,467,375 | T/C | — | uncertain significance |
| rs749664782 | 2:164,467,396 | G/A | — | uncertain significance |
| rs748294735 | 2:164,467,468 | C/T | — | uncertain significance |
| rs866216827 | 2:164,467,491 | G/A | — | uncertain significance |
| rs776413594 | 2:164,467,523 | C/T | — | likely benign |
| rs756271439 | 2:164,467,547 | C/T | — | likely benign |
| rs2467840001 | 2:164,467,602 | T/G | — | uncertain significance |
| rs751576888 | 2:164,467,632 | T/C | — | uncertain significance |
| rs2467840140 | 2:164,467,652 | T/A | — | likely benign |
| rs775473694 | 2:164,467,845 | C/T | — | uncertain significance |
| rs900271392 | 2:164,467,888 | G/A | — | uncertain significance |
| rs2467840942 | 2:164,467,959 | A/T | — | uncertain significance |
| rs201440665 | 2:164,467,966 | C/T | — | uncertain significance |
| rs375294645 | 2:164,467,968 | G/A | — | uncertain significance |
| rs778596686 | 2:164,468,037 | C/T | — | uncertain significance |
| rs368385434 | 2:164,468,098 | G/A | — | uncertain significance |
| rs777998583 | 2:164,468,197 | T/C | — | uncertain significance |
| rs982393 | 2:164,490,529 | A/T | intron variant | — |
| rs56328583 | 2:164,523,801 | C/G | — | — |
| rs28473311 | 2:164,573,847 | C/G | intron variant | — |
| rs80163246 | 2:164,574,344 | T/C | regulatory region variant | — |
| rs1460678 | 2:164,584,156 | C/G | intron variant | — |
| rs9287838 | 2:164,585,004 | G/A | — | — |
| rs62173861 | 2:164,593,148 | C/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.