MICAL2
microtubule associated monooxygenase, calponin and LIM domain containing 2
Summary
The protein encoded by this gene is a monooxygenase that enhances depolymerization of F-actin and is therefore involved in cytoskeletal dynamics. The encoded protein is a regulator of the SRF signaling pathway. Increased expression of this gene has been associated with cancer progression and metastasis. [provided by RefSeq, Oct 2016]
Known Variants146 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1994318 | 11:12,159,661 | C/A | regulatory region variant | — |
| rs1017723028 | 11:12,183,710 | A/T | — | uncertain significance |
| rs1189253030 | 11:12,183,717 | G/C | — | uncertain significance |
| rs1485101994 | 11:12,183,721 | G/A | — | uncertain significance |
| rs964421576 | 11:12,183,785 | C/G | — | uncertain significance |
| rs141382782 | 11:12,183,822 | C/A | — | uncertain significance |
| rs77782413 | 11:12,183,823 | C/G | — | conflicting classifications of pathogenicity |
| rs375504985 | 11:12,183,832 | C/G | — | uncertain significance |
| rs749392019 | 11:12,183,917 | G/A | — | uncertain significance |
| rs1212364149 | 11:12,183,927 | C/A | — | uncertain significance |
| rs1332950505 | 11:12,183,962 | C/A | — | uncertain significance |
| rs17477949 | 11:12,219,203 | C/T | intron variant | — |
| rs774020963 | 11:12,225,803 | A/T | — | uncertain significance |
| rs755905050 | 11:12,225,849 | C/A | — | uncertain significance |
| rs773933327 | 11:12,225,872 | G/A | — | uncertain significance |
| rs2496345467 | 11:12,225,942 | T/A | — | uncertain significance |
| rs774881551 | 11:12,225,996 | A/G | — | uncertain significance |
| rs149218318 | 11:12,229,611 | A/T | — | uncertain significance |
| rs1257869145 | 11:12,231,071 | C/T | — | uncertain significance |
| rs2496428341 | 11:12,231,110 | T/C | — | uncertain significance |
| rs145597085 | 11:12,231,120 | C/T | synonymous variant | — |
| rs1855743107 | 11:12,234,829 | A/T | — | uncertain significance |
| rs750975984 | 11:12,234,877 | C/T | — | uncertain significance |
| rs1350500856 | 11:12,234,924 | C/G | — | uncertain significance |
| rs777916894 | 11:12,237,853 | G/A | — | uncertain significance |
| rs150558972 | 11:12,240,474 | C/G | intron variant | — |
| rs2496622849 | 11:12,241,748 | G/C | — | uncertain significance |
| rs369887102 | 11:12,241,779 | C/T | — | uncertain significance |
| rs545376692 | 11:12,241,817 | C/T | — | uncertain significance |
| rs144642828 | 11:12,241,818 | G/A | — | uncertain significance |
| rs202206049 | 11:12,241,934 | A/T | — | uncertain significance |
| rs140391872 | 11:12,241,950 | G/A | — | uncertain significance |
| rs200883778 | 11:12,242,009 | C/T | — | likely benign |
| rs780210943 | 11:12,243,222 | G/A | — | uncertain significance |
| rs200623078 | 11:12,243,264 | G/A | — | likely benign |
| rs1410860607 | 11:12,243,271 | C/A | — | uncertain significance |
| rs757670405 | 11:12,243,290 | G/A | — | uncertain significance |
| rs375247527 | 11:12,244,199 | C/T | — | uncertain significance |
| rs551546075 | 11:12,246,239 | C/A | — | uncertain significance |
| rs571399686 | 11:12,246,240 | A/G | — | uncertain significance |
| rs757968579 | 11:12,246,297 | G/A | — | uncertain significance |
| rs748545295 | 11:12,246,309 | T/A | — | uncertain significance |
| rs370855282 | 11:12,246,316 | G/A | — | uncertain significance |
| rs138170636 | 11:12,246,354 | C/T | — | uncertain significance |
| rs35387130 | 11:12,246,355 | G/A | — | benign |
| rs2496754709 | 11:12,247,741 | A/G | — | uncertain significance |
| rs184076407 | 11:12,247,851 | C/T | — | uncertain significance |
| rs142377929 | 11:12,247,860 | G/T | — | uncertain significance |
| rs762245573 | 11:12,247,897 | G/T | — | uncertain significance |
| rs951402098 | 11:12,247,899 | A/T | — | uncertain significance |
| rs972563428 | 11:12,247,914 | G/A | — | uncertain significance |
| rs35228638 | 11:12,248,590 | A/G | — | benign |
| rs1857574325 | 11:12,248,635 | A/G | — | uncertain significance |
| rs146540356 | 11:12,248,649 | C/T | — | uncertain significance |
| rs769329735 | 11:12,248,676 | C/T | — | uncertain significance |
| rs1330405360 | 11:12,257,761 | G/A | — | uncertain significance |
| rs202081792 | 11:12,257,778 | A/G | — | uncertain significance |
| rs2496941232 | 11:12,261,053 | A/C | — | uncertain significance |
| rs371411174 | 11:12,261,107 | C/T | — | uncertain significance |
| rs761260855 | 11:12,261,109 | C/T | — | uncertain significance |
| rs2496942701 | 11:12,261,116 | C/T | — | uncertain significance |
| rs753200392 | 11:12,262,590 | C/T | — | uncertain significance |
| rs376168249 | 11:12,262,591 | G/A | — | uncertain significance |
| rs531909303 | 11:12,262,634 | C/T | — | likely benign |
| rs200663760 | 11:12,263,780 | C/T | — | uncertain significance |
| rs1166042941 | 11:12,263,906 | C/G | — | uncertain significance |
| rs756958104 | 11:12,263,947 | C/T | — | uncertain significance |
| rs375386842 | 11:12,263,948 | G/A | — | uncertain significance |
| rs758394455 | 11:12,263,954 | A/G | — | uncertain significance |
| rs746485317 | 11:12,263,964 | G/T | — | uncertain significance |
| rs2496991314 | 11:12,263,965 | G/C | — | uncertain significance |
| rs780768530 | 11:12,264,224 | G/A | — | uncertain significance |
| rs2496998640 | 11:12,264,270 | A/G | — | uncertain significance |
| rs146142372 | 11:12,264,276 | C/T | — | uncertain significance |
| rs148802800 | 11:12,264,293 | A/T | — | uncertain significance |
| rs779266555 | 11:12,264,315 | C/T | — | uncertain significance |
| rs748304331 | 11:12,265,562 | A/G | — | uncertain significance |
| rs770107867 | 11:12,265,564 | A/G | — | uncertain significance |
| rs969208728 | 11:12,265,615 | T/G | — | uncertain significance |
| rs1380350357 | 11:12,270,743 | C/T | — | uncertain significance |
| rs553285474 | 11:12,270,750 | G/T | — | uncertain significance |
| rs542038120 | 11:12,270,764 | C/T | — | uncertain significance |
| rs147611377 | 11:12,277,191 | T/G | — | uncertain significance |
| rs147838643 | 11:12,277,214 | G/A | — | uncertain significance |
| rs2134646647 | 11:12,277,245 | A/G | — | uncertain significance |
| rs2497165334 | 11:12,277,293 | A/G | — | uncertain significance |
| rs201529406 | 11:12,278,335 | T/A | — | uncertain significance |
| rs780747971 | 11:12,278,407 | G/A | — | uncertain significance |
| rs574121025 | 11:12,278,410 | A/G | — | uncertain significance |
| rs61877173 | 11:12,278,417 | G/A | — | uncertain significance |
| rs374855539 | 11:12,278,447 | G/A | — | uncertain significance |
| rs368099985 | 11:12,278,486 | G/A | — | uncertain significance |
| rs869025227 | 11:12,278,507 | A/G | — | uncertain significance |
| rs2497198810 | 11:12,280,093 | A/C | — | uncertain significance |
| rs1027334 | 11:12,281,353 | A/G | — | benign |
| rs1197414188 | 11:12,281,421 | G/A | — | uncertain significance |
| rs1027335 | 11:12,281,427 | T/C | — | benign |
| rs113124121 | 11:12,281,537 | G/T | — | likely benign |
| rs774468064 | 11:12,313,753 | T/A | — | uncertain significance |
| rs746061557 | 11:12,313,839 | C/T | — | uncertain significance |
Showing 100 of 146 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.