ABLIM3
actin binding LIM protein family member 3
Summary
This gene encodes a member of the actin-binding LIM (abLIM) family of proteins. These proteins are characterized by an N-terminal LIM domain and a C-terminal dematin-like domain. The encoded protein interacts with actin filaments and may be a component of adherens junctions in several cell types. A variant of this gene may be associated with pain sensitivity in male human patients. [provided by RefSeq, Sep 2016]
Known Variants62 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs4134361 | 5:148,527,101 | G/C | intron variant | — |
| rs7714046 | 5:148,550,501 | T/A | — | — |
| rs768003190 | 5:148,563,059 | G/A | — | uncertain significance |
| rs10875646 | 5:148,564,757 | A/T | — | — |
| rs10463416 | 5:148,572,915 | G/A | intron variant | — |
| rs4235743 | 5:148,573,649 | C/T | intron variant | — |
| rs7720260 | 5:148,576,253 | T/C | intron variant | — |
| rs778989066 | 5:148,577,872 | G/A | — | uncertain significance |
| rs750610592 | 5:148,577,881 | G/A | — | uncertain significance |
| rs1385473956 | 5:148,577,886 | C/T | — | uncertain significance |
| rs199548691 | 5:148,577,887 | G/A | — | uncertain significance |
| rs750466880 | 5:148,577,949 | G/A | — | uncertain significance |
| rs774374268 | 5:148,579,893 | T/C | — | uncertain significance |
| rs76939309 | 5:148,579,975 | G/A | — | benign |
| rs186503737 | 5:148,586,579 | G/A | — | uncertain significance |
| rs759481034 | 5:148,586,585 | A/G | — | uncertain significance |
| rs767983995 | 5:148,596,564 | C/T | — | uncertain significance |
| rs376872688 | 5:148,610,217 | G/A | — | uncertain significance |
| rs1400412856 | 5:148,610,236 | G/A | — | uncertain significance |
| rs758578982 | 5:148,610,250 | C/T | — | uncertain significance |
| rs114575408 | 5:148,610,251 | G/A | — | uncertain significance |
| rs1011400 | 5:148,611,941 | G/A | — | — |
| rs1449115415 | 5:148,612,813 | T/C | — | uncertain significance |
| rs1223711292 | 5:148,612,862 | G/A | — | uncertain significance |
| rs1270449365 | 5:148,617,012 | C/T | — | uncertain significance |
| rs756449768 | 5:148,617,080 | G/A | — | uncertain significance |
| rs149749871 | 5:148,617,090 | G/A | — | uncertain significance |
| rs556018790 | 5:148,617,117 | A/T | — | uncertain significance |
| rs2480759260 | 5:148,618,821 | C/T | — | uncertain significance |
| rs148352775 | 5:148,619,331 | G/A | — | uncertain significance |
| rs150488528 | 5:148,619,346 | C/G | — | uncertain significance |
| rs142716823 | 5:148,619,368 | C/T | — | uncertain significance |
| rs552321551 | 5:148,619,398 | G/A | — | uncertain significance |
| rs2480770726 | 5:148,619,408 | G/A | — | uncertain significance |
| rs147351594 | 5:148,619,424 | C/T | — | uncertain significance |
| rs143929547 | 5:148,620,322 | C/A | — | uncertain significance |
| rs61733085 | 5:148,622,082 | C/A | — | benign |
| rs368153520 | 5:148,622,083 | C/T | — | uncertain significance |
| rs61744926 | 5:148,622,085 | G/A | — | benign |
| rs139404389 | 5:148,622,095 | C/T | — | uncertain significance |
| rs759188635 | 5:148,624,486 | T/C | — | uncertain significance |
| rs756456127 | 5:148,624,512 | A/G | — | uncertain significance |
| rs1295692341 | 5:148,624,560 | T/C | — | uncertain significance |
| rs1348374121 | 5:148,626,085 | T/G | — | uncertain significance |
| rs148988138 | 5:148,626,095 | C/T | — | uncertain significance |
| rs369536848 | 5:148,626,096 | G/A | — | uncertain significance |
| rs1753528127 | 5:148,627,375 | A/C | — | uncertain significance |
| rs386352275 | 5:148,627,377 | G/A | — | uncertain significance |
| rs199889968 | 5:148,627,400 | G/A | — | uncertain significance |
| rs567315993 | 5:148,627,420 | A/G | — | uncertain significance |
| rs138587496 | 5:148,627,430 | G/A | — | uncertain significance |
| rs142642160 | 5:148,627,438 | A/G | — | uncertain significance |
| rs386352274 | 5:148,627,458 | G/A | — | uncertain significance |
| rs776050391 | 5:148,627,478 | T/C | — | uncertain significance |
| rs761389232 | 5:148,629,387 | C/T | — | uncertain significance |
| rs1421226226 | 5:148,630,012 | C/T | — | uncertain significance |
| rs2480878594 | 5:148,630,018 | A/T | — | uncertain significance |
| rs771233493 | 5:148,630,066 | A/G | — | uncertain significance |
| rs781176765 | 5:148,630,925 | C/T | — | uncertain significance |
| rs770290671 | 5:148,630,949 | G/A | — | uncertain significance |
| rs979930405 | 5:148,637,957 | G/A | — | uncertain significance |
| rs529496414 | 5:148,639,800 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.