MICAL3
microtubule associated monooxygenase, calponin and LIM domain containing 3
Summary
Enables actin binding activity and molecular adaptor activity. Involved in actin filament depolymerization. Located in several cellular components, including Flemming body; intercellular bridge; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants170 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs183092756 | 22:18,273,641 | T/C | — | uncertain significance |
| rs115182420 | 22:18,273,976 | C/A | — | benign |
| rs61743624 | 22:18,273,978 | G/A | — | likely benign |
| rs760179971 | 22:18,273,983 | G/A | — | uncertain significance |
| rs5992105 | 22:18,283,247 | A/G | regulatory region variant | — |
| rs5992106 | 22:18,283,916 | T/A | — | — |
| rs375603 | 22:18,284,420 | G/C | intron variant | — |
| rs748416314 | 22:18,291,627 | G/A | — | uncertain significance |
| rs76474025 | 22:18,291,643 | C/T | — | uncertain significance |
| rs1480640890 | 22:18,291,649 | T/C | — | uncertain significance |
| rs558756509 | 22:18,291,661 | G/A | — | uncertain significance |
| rs371784330 | 22:18,291,663 | C/T | — | uncertain significance |
| rs2518766224 | 22:18,291,666 | T/C | — | uncertain significance |
| rs763294962 | 22:18,293,486 | G/A | — | uncertain significance |
| rs201337842 | 22:18,293,533 | C/T | — | uncertain significance |
| rs781511126 | 22:18,293,541 | C/G | — | likely benign |
| rs200100943 | 22:18,293,572 | G/A | — | uncertain significance |
| rs750739956 | 22:18,299,464 | G/A | — | uncertain significance |
| rs201187618 | 22:18,299,495 | G/A | — | likely benign |
| rs1335282820 | 22:18,299,507 | G/T | — | uncertain significance |
| rs201041100 | 22:18,299,535 | C/T | — | uncertain significance |
| rs888455219 | 22:18,299,538 | C/T | — | uncertain significance |
| rs1921115335 | 22:18,300,088 | A/T | — | uncertain significance |
| rs200437633 | 22:18,300,098 | C/T | — | likely benign |
| rs2518786193 | 22:18,300,103 | T/G | — | uncertain significance |
| rs1431557366 | 22:18,300,122 | T/C | — | uncertain significance |
| rs1373919614 | 22:18,300,125 | C/T | — | uncertain significance |
| rs751534126 | 22:18,300,184 | T/C | — | uncertain significance |
| rs186055762 | 22:18,300,200 | C/T | — | uncertain significance |
| rs749902831 | 22:18,300,349 | C/A | — | uncertain significance |
| rs1187845941 | 22:18,300,350 | T/C | — | uncertain significance |
| rs566820936 | 22:18,300,403 | G/A | — | uncertain significance |
| rs2518787039 | 22:18,300,445 | G/C | — | uncertain significance |
| rs45518631 | 22:18,300,470 | G/T | — | likely benign |
| rs369106641 | 22:18,300,493 | C/T | — | uncertain significance |
| rs758742610 | 22:18,300,494 | G/A | — | uncertain significance |
| rs963856119 | 22:18,300,502 | C/T | — | uncertain significance |
| rs775830864 | 22:18,300,523 | G/A | — | uncertain significance |
| rs779023205 | 22:18,300,598 | C/T | — | uncertain significance |
| rs780716515 | 22:18,300,667 | G/T | — | uncertain significance |
| rs560819207 | 22:18,300,679 | G/C | — | uncertain significance |
| rs560519874 | 22:18,300,706 | G/A | — | uncertain significance |
| rs370318089 | 22:18,300,710 | C/T | — | uncertain significance |
| rs200812565 | 22:18,300,757 | C/T | — | uncertain significance |
| rs2518787730 | 22:18,300,764 | T/C | — | uncertain significance |
| rs548921349 | 22:18,300,772 | C/T | — | uncertain significance |
| rs199944756 | 22:18,300,787 | G/A | — | uncertain significance |
| rs369717291 | 22:18,300,898 | C/T | — | uncertain significance |
| rs373213687 | 22:18,300,932 | G/C | — | uncertain significance |
| rs138062653 | 22:18,300,940 | C/T | — | uncertain significance |
| rs199672102 | 22:18,300,947 | A/C | — | conflicting classifications of pathogenicity |
| rs761904383 | 22:18,300,953 | C/G | — | uncertain significance |
| rs780678345 | 22:18,300,964 | G/A | — | uncertain significance |
| rs774870093 | 22:18,300,979 | G/A | — | uncertain significance |
| rs2518788174 | 22:18,300,982 | T/C | — | likely benign |
| rs766517694 | 22:18,301,009 | C/T | — | uncertain significance |
| rs375690426 | 22:18,301,010 | G/A | — | uncertain significance |
| rs1173335387 | 22:18,301,038 | T/G | — | likely benign |
| rs771139321 | 22:18,301,067 | T/C | — | uncertain significance |
| rs777028329 | 22:18,301,071 | C/A | — | uncertain significance |
| rs568643015 | 22:18,301,171 | C/T | — | uncertain significance |
| rs534856649 | 22:18,301,184 | C/T | — | uncertain significance |
| rs73382765 | 22:18,301,190 | G/A | — | benign |
| rs143411730 | 22:18,301,214 | G/A | — | uncertain significance |
| rs760595870 | 22:18,301,216 | G/C | — | uncertain significance |
| rs770858360 | 22:18,301,219 | G/A | — | uncertain significance |
| rs756299375 | 22:18,301,243 | T/G | — | uncertain significance |
| rs751011868 | 22:18,301,309 | T/C | — | uncertain significance |
| rs200625626 | 22:18,301,325 | C/T | — | uncertain significance |
| rs541380717 | 22:18,301,348 | G/A | — | uncertain significance |
| rs368880854 | 22:18,301,423 | C/T | — | uncertain significance |
| rs1289121545 | 22:18,301,433 | C/A | — | uncertain significance |
| rs148613283 | 22:18,301,508 | C/T | — | likely benign |
| rs750173882 | 22:18,301,537 | G/T | — | uncertain significance |
| rs73876508 | 22:18,301,570 | G/A | — | benign |
| rs747674587 | 22:18,301,586 | G/A | — | likely benign |
| rs2146009528 | 22:18,301,588 | A/G | — | uncertain significance |
| rs1028483030 | 22:18,301,610 | G/A | — | uncertain significance |
| rs776990932 | 22:18,301,618 | G/A | — | uncertain significance |
| rs368048560 | 22:18,301,702 | G/A | — | uncertain significance |
| rs369894156 | 22:18,301,744 | A/T | — | uncertain significance |
| rs555800332 | 22:18,301,756 | C/T | — | uncertain significance |
| rs755339826 | 22:18,301,820 | G/A | — | uncertain significance |
| rs765184052 | 22:18,301,840 | C/T | — | uncertain significance |
| rs369298683 | 22:18,301,873 | G/C | — | uncertain significance |
| rs1016912017 | 22:18,304,239 | T/C | — | uncertain significance |
| rs375696139 | 22:18,304,245 | G/A | — | uncertain significance |
| rs200224924 | 22:18,304,248 | C/T | — | uncertain significance |
| rs186745892 | 22:18,304,804 | T/C | — | benign |
| rs747994390 | 22:18,304,820 | C/T | — | uncertain significance |
| rs200633079 | 22:18,304,843 | G/A | — | uncertain significance |
| rs1921713125 | 22:18,304,886 | G/A | — | uncertain significance |
| rs1921714300 | 22:18,304,918 | C/G | — | uncertain significance |
| rs369532856 | 22:18,305,767 | C/T | — | uncertain significance |
| rs750434835 | 22:18,305,776 | C/T | — | uncertain significance |
| rs772622205 | 22:18,305,824 | G/A | — | uncertain significance |
| rs1393312968 | 22:18,310,413 | C/T | — | likely benign |
| rs563233019 | 22:18,310,436 | G/A | — | uncertain significance |
| rs773016318 | 22:18,310,452 | C/G | — | uncertain significance |
| rs758019211 | 22:18,310,481 | T/G | — | uncertain significance |
Showing 100 of 170 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.