ABLIM2
actin binding LIM protein family member 2
Summary
Predicted to enable actin filament binding activity. Predicted to be involved in lamellipodium assembly. Predicted to act upstream of or within positive regulation of transcription by RNA polymerase II. Located in actin cytoskeleton. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants60 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2545417379 | 4:7,968,742 | A/G | — | uncertain significance |
| rs571203819 | 4:7,969,924 | C/A | — | — |
| rs747471823 | 4:7,985,011 | C/T | — | uncertain significance |
| rs374407006 | 4:7,985,028 | A/G | — | uncertain significance |
| rs750016618 | 4:7,985,031 | C/T | — | uncertain significance |
| rs200508979 | 4:7,985,047 | C/T | — | uncertain significance |
| rs1285314481 | 4:7,986,591 | G/T | — | uncertain significance |
| rs957121311 | 4:7,986,598 | C/T | — | uncertain significance |
| rs1462247852 | 4:7,986,607 | G/T | — | uncertain significance |
| rs375119926 | 4:7,986,613 | T/C | — | uncertain significance |
| rs201611635 | 4:7,994,594 | C/T | — | uncertain significance |
| rs41266509 | 4:7,994,726 | G/T | intron variant | — |
| rs766457929 | 4:8,009,823 | G/T | — | uncertain significance |
| rs375623912 | 4:8,009,888 | T/C | — | uncertain significance |
| rs1311703718 | 4:8,010,807 | C/A | — | uncertain significance |
| rs774733942 | 4:8,010,827 | C/A | — | uncertain significance |
| rs868504646 | 4:8,021,932 | G/C | — | uncertain significance |
| rs368630237 | 4:8,021,935 | C/T | — | uncertain significance |
| rs760544443 | 4:8,021,957 | C/G | — | uncertain significance |
| rs187056157 | 4:8,021,976 | G/A | — | uncertain significance |
| rs375921912 | 4:8,021,995 | C/T | — | uncertain significance |
| rs776250088 | 4:8,022,027 | C/T | — | uncertain significance |
| rs2547255592 | 4:8,029,572 | C/T | — | uncertain significance |
| rs547044955 | 4:8,031,427 | C/T | — | uncertain significance |
| rs111255429 | 4:8,031,487 | C/T | — | uncertain significance |
| rs768462513 | 4:8,037,896 | C/A | — | uncertain significance |
| rs200191701 | 4:8,037,944 | G/A | — | uncertain significance |
| rs560311179 | 4:8,039,229 | G/T | — | — |
| rs11931521 | 4:8,043,700 | A/G | intron variant | — |
| rs757458512 | 4:8,046,907 | G/A | — | uncertain significance |
| rs201328445 | 4:8,046,928 | G/A | — | uncertain significance |
| rs185934307 | 4:8,055,963 | G/C | — | uncertain significance |
| rs6811028 | 4:8,062,689 | T/C | — | benign |
| rs10938683 | 4:8,062,690 | G/A | — | benign |
| rs756529150 | 4:8,062,725 | C/T | — | uncertain significance |
| rs369935153 | 4:8,079,363 | C/T | — | uncertain significance |
| rs202211361 | 4:8,079,385 | A/G | — | likely benign |
| rs375896292 | 4:8,079,398 | C/T | — | uncertain significance |
| rs370597514 | 4:8,079,399 | G/A | — | uncertain significance |
| rs778115675 | 4:8,079,414 | C/T | — | likely benign |
| rs1288190877 | 4:8,082,404 | T/G | — | uncertain significance |
| rs1561236738 | 4:8,082,457 | C/A | — | uncertain significance |
| rs34049746 | 4:8,082,472 | T/C | — | uncertain significance |
| rs780667383 | 4:8,082,515 | C/T | — | uncertain significance |
| rs2546261496 | 4:8,089,905 | C/T | — | uncertain significance |
| rs371815593 | 4:8,089,920 | C/T | — | uncertain significance |
| rs947707877 | 4:8,089,926 | T/G | — | uncertain significance |
| rs190189401 | 4:8,089,932 | C/T | — | likely benign |
| rs747138981 | 4:8,090,002 | G/T | — | uncertain significance |
| rs764119014 | 4:8,098,833 | C/T | — | uncertain significance |
| rs751566556 | 4:8,098,842 | C/T | — | uncertain significance |
| rs199762433 | 4:8,098,870 | C/A | — | likely benign |
| rs2546611171 | 4:8,098,914 | A/C | — | uncertain significance |
| rs202014516 | 4:8,098,926 | C/T | — | uncertain significance |
| rs780709611 | 4:8,098,955 | A/G | — | uncertain significance |
| rs556771279 | 4:8,098,983 | C/T | — | uncertain significance |
| rs760268567 | 4:8,108,265 | C/T | — | uncertain significance |
| rs752430305 | 4:8,108,316 | G/A | — | uncertain significance |
| rs371949822 | 4:8,108,337 | G/A | — | uncertain significance |
| rs13151374 | 4:8,122,221 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.