LIMCH1
LIM and calponin homology domains 1
Summary
Enables myosin II head/neck binding activity. Involved in several processes, including cytoplasmic actin-based contraction involved in cell motility; positive regulation of stress fiber assembly; and regulation of focal adhesion assembly. Located in myosin II complex and stress fiber. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants81 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1343349811 | 4:41,362,910 | C/A | — | uncertain significance |
| rs1214039735 | 4:41,362,916 | C/G | — | uncertain significance |
| rs4349633 | 4:41,485,212 | G/T | — | — |
| rs550262915 | 4:41,489,858 | A/G | — | — |
| rs1203963130 | 4:41,496,569 | G/A | — | uncertain significance |
| rs1554072557 | 4:41,496,610 | A/G | — | uncertain significance |
| rs141075683 | 4:41,601,021 | A/G | — | uncertain significance |
| rs2551845070 | 4:41,605,900 | A/T | — | uncertain significance |
| rs756416654 | 4:41,607,971 | A/G | — | uncertain significance |
| rs146838350 | 4:41,607,998 | G/A | — | uncertain significance |
| rs2551867571 | 4:41,615,630 | T/G | — | uncertain significance |
| rs531782327 | 4:41,615,633 | C/T | — | uncertain significance |
| rs2551867614 | 4:41,615,639 | A/C | — | uncertain significance |
| rs2551886128 | 4:41,621,289 | C/G | — | uncertain significance |
| rs147408540 | 4:41,621,367 | C/T | missense variant | uncertain significance |
| rs769827569 | 4:41,621,406 | G/T | — | uncertain significance |
| rs766254213 | 4:41,621,423 | G/A | — | uncertain significance |
| rs187942563 | 4:41,634,826 | G/A | — | likely benign |
| rs4345220 | 4:41,639,516 | A/T | — | — |
| rs778372980 | 4:41,646,527 | A/G | — | uncertain significance |
| rs868697031 | 4:41,646,558 | C/T | — | uncertain significance |
| rs542134097 | 4:41,648,150 | G/A | — | uncertain significance |
| rs140689582 | 4:41,648,507 | G/A | — | uncertain significance |
| rs771647731 | 4:41,648,545 | C/T | — | uncertain significance |
| rs2094069444 | 4:41,648,554 | G/C | — | uncertain significance |
| rs754453432 | 4:41,648,561 | C/T | — | uncertain significance |
| rs777885509 | 4:41,648,599 | A/G | — | uncertain significance |
| rs749018621 | 4:41,648,621 | G/T | — | uncertain significance |
| rs373341850 | 4:41,648,654 | A/G | — | uncertain significance |
| rs143733086 | 4:41,648,713 | C/T | — | uncertain significance |
| rs767672193 | 4:41,648,714 | G/A | — | uncertain significance |
| rs148133956 | 4:41,648,767 | G/A | — | likely benign |
| rs763515008 | 4:41,648,773 | G/A | — | likely benign |
| rs2551961335 | 4:41,648,823 | A/T | — | uncertain significance |
| rs138689621 | 4:41,648,825 | C/T | — | uncertain significance |
| rs769175851 | 4:41,648,858 | C/T | — | uncertain significance |
| rs200620612 | 4:41,648,862 | G/C | — | uncertain significance |
| rs199602150 | 4:41,648,894 | T/G | — | uncertain significance |
| rs2094084715 | 4:41,648,902 | A/G | — | uncertain significance |
| rs751602376 | 4:41,652,416 | G/A | — | uncertain significance |
| rs201089774 | 4:41,652,426 | G/C | — | uncertain significance |
| rs562812091 | 4:41,652,441 | C/T | — | uncertain significance |
| rs1422273805 | 4:41,652,494 | C/T | — | uncertain significance |
| rs147874816 | 4:41,652,521 | G/A | — | uncertain significance |
| rs201825715 | 4:41,652,522 | A/G | — | uncertain significance |
| rs760282270 | 4:41,652,525 | G/C | — | uncertain significance |
| rs906644326 | 4:41,652,609 | T/C | — | uncertain significance |
| rs143987835 | 4:41,652,622 | C/T | — | likely benign |
| rs751880453 | 4:41,663,443 | A/C | — | uncertain significance |
| rs1026853917 | 4:41,663,467 | C/G | — | uncertain significance |
| rs780277346 | 4:41,663,471 | A/G | — | uncertain significance |
| rs139738687 | 4:41,663,489 | G/A | — | likely benign |
| rs57547885 | 4:41,663,518 | G/A | — | uncertain significance |
| rs184117721 | 4:41,664,841 | C/T | — | uncertain significance |
| rs200351703 | 4:41,664,868 | G/A | — | uncertain significance |
| rs759582356 | 4:41,664,875 | C/A | — | uncertain significance |
| rs538025734 | 4:41,664,894 | G/A | — | uncertain significance |
| rs1001793203 | 4:41,664,941 | A/C | — | uncertain significance |
| rs2094680531 | 4:41,664,988 | T/C | — | uncertain significance |
| rs1244018648 | 4:41,664,991 | T/C | — | uncertain significance |
| rs761754320 | 4:41,668,606 | A/G | — | uncertain significance |
| rs138567175 | 4:41,668,624 | C/T | — | uncertain significance |
| rs149292265 | 4:41,668,651 | A/G | — | uncertain significance |
| rs145925686 | 4:41,678,433 | G/A | — | uncertain significance |
| rs374330346 | 4:41,678,468 | C/T | — | uncertain significance |
| rs2552079298 | 4:41,682,042 | A/C | — | uncertain significance |
| rs1714415172 | 4:41,682,069 | A/G | — | uncertain significance |
| rs757204155 | 4:41,682,111 | A/G | — | uncertain significance |
| rs199980656 | 4:41,683,026 | G/A | — | uncertain significance |
| rs747438665 | 4:41,684,385 | A/C | — | uncertain significance |
| rs1046288262 | 4:41,686,468 | T/G | — | uncertain significance |
| rs772281959 | 4:41,686,475 | C/T | — | uncertain significance |
| rs61745963 | 4:41,686,520 | C/T | — | likely benign |
| rs2552084744 | 4:41,687,755 | T/A | — | uncertain significance |
| rs149115624 | 4:41,687,764 | C/A | — | uncertain significance |
| rs771835427 | 4:41,687,807 | A/G | — | uncertain significance |
| rs941497609 | 4:41,687,825 | G/A | — | uncertain significance |
| rs370336529 | 4:41,687,844 | G/A | — | uncertain significance |
| rs369048287 | 4:41,689,868 | G/T | — | uncertain significance |
| rs140341643 | 4:41,689,913 | C/G | — | uncertain significance |
| rs780764464 | 4:41,691,599 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.