ACTL7B
actin like 7B
Summary
The protein encoded by this gene is a member of a family of actin-related proteins (ARPs) which share significant amino acid sequence identity to conventional actins. Both actins and ARPs have an actin fold, which is an ATP-binding cleft, as a common feature. The ARPs are involved in diverse cellular processes, including vesicular transport, spindle orientation, nuclear migration and chromatin remodeling. This gene (ACTL7B), and related gene, ACTL7A, are intronless, and are located approximately 4 kb apart in a head-to-head orientation within the familial dysautonomia candidate region on 9q31. Based on mutational analysis of the ACTL7B gene in patients with this disorder, it was concluded that it is unlikely to be involved in the pathogenesis of dysautonomia. Unlike ACTL7A, the ACTL7B gene is expressed predominantly in the testis, however, its exact function is not known. [provided by RefSeq, Jul 2008]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs752064414 | 9:111,617,139 | C/T | — | uncertain significance |
| rs753089435 | 9:111,617,151 | G/A | — | uncertain significance |
| rs114143830 | 9:111,617,174 | G/C | — | benign |
| rs1271933655 | 9:111,617,288 | G/A | — | likely benign |
| rs2537880390 | 9:111,617,340 | T/C | — | uncertain significance |
| rs566851763 | 9:111,617,345 | A/G | — | uncertain significance |
| rs140336222 | 9:111,617,355 | C/T | — | uncertain significance |
| rs1301600694 | 9:111,617,367 | C/T | — | uncertain significance |
| rs369622245 | 9:111,617,390 | G/A | — | likely benign |
| rs150394114 | 9:111,617,422 | G/T | — | benign |
| rs2537824176 | 9:111,617,429 | T/A | — | uncertain significance |
| rs143927577 | 9:111,617,553 | T/A | — | uncertain significance |
| rs146541685 | 9:111,617,555 | G/A | — | uncertain significance |
| rs1382113416 | 9:111,617,579 | T/C | — | uncertain significance |
| rs758565813 | 9:111,617,582 | G/A | — | uncertain significance |
| rs150518659 | 9:111,617,679 | C/T | — | uncertain significance |
| rs2537825144 | 9:111,617,718 | C/T | — | uncertain significance |
| rs1267790926 | 9:111,617,721 | C/T | — | uncertain significance |
| rs2537825158 | 9:111,617,730 | C/T | — | uncertain significance |
| rs1407009912 | 9:111,617,744 | G/A | — | uncertain significance |
| rs145110192 | 9:111,617,757 | G/A | — | uncertain significance |
| rs2537825207 | 9:111,617,769 | G/T | — | uncertain significance |
| rs149121708 | 9:111,617,776 | G/C | — | uncertain significance |
| rs1165083441 | 9:111,617,787 | G/C | — | uncertain significance |
| rs142207473 | 9:111,617,790 | G/C | — | uncertain significance |
| rs372513303 | 9:111,617,847 | C/T | — | uncertain significance |
| rs911946010 | 9:111,617,871 | G/A | — | uncertain significance |
| rs755792266 | 9:111,617,984 | G/A | — | uncertain significance |
| rs150446824 | 9:111,618,014 | G/A | — | uncertain significance |
| rs767799116 | 9:111,618,056 | A/G | — | uncertain significance |
| rs1827093804 | 9:111,618,057 | C/T | — | likely benign |
| rs138263222 | 9:111,618,080 | C/A | — | uncertain significance |
| rs1381739827 | 9:111,618,093 | T/C | — | uncertain significance |
| rs1259000718 | 9:111,618,104 | G/C | — | uncertain significance |
| rs763647244 | 9:111,618,132 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.