ACTL9
actin like 9
Summary
Involved in acrosome assembly and fertilization. Located in acrosomal vesicle; perinuclear theca; and sperm head. Implicated in spermatogenic failure 53. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs34687433 | 19:8,807,843 | G/C | — | pathogenic |
| rs112957538 | 19:8,807,853 | C/T | — | likely benign |
| rs1555753234 | 19:8,807,859 | A/G | — | uncertain significance |
| rs781910740 | 19:8,807,881 | G/T | — | uncertain significance |
| rs532021673 | 19:8,807,914 | C/A | — | pathogenic |
| rs1478948010 | 19:8,808,018 | G/A | — | pathogenic |
| rs782009335 | 19:8,808,041 | G/C | — | uncertain significance |
| rs782429705 | 19:8,808,051 | A/G | — | uncertain significance |
| rs2512730201 | 19:8,808,097 | C/A | — | uncertain significance |
| rs781996157 | 19:8,808,177 | T/C | — | uncertain significance |
| rs373541326 | 19:8,808,196 | G/A | — | uncertain significance |
| rs2043206967 | 19:8,808,210 | T/C | — | uncertain significance |
| rs1555753339 | 19:8,808,229 | C/T | — | uncertain significance |
| rs374419357 | 19:8,808,264 | G/C | — | uncertain significance |
| rs142929347 | 19:8,808,271 | C/T | — | uncertain significance |
| rs781854741 | 19:8,808,298 | C/T | — | uncertain significance |
| rs987371604 | 19:8,808,370 | G/C | — | uncertain significance |
| rs139329295 | 19:8,808,430 | C/T | — | uncertain significance |
| rs782544746 | 19:8,808,442 | A/T | — | uncertain significance |
| rs782170839 | 19:8,808,451 | C/T | — | uncertain significance |
| rs146070515 | 19:8,808,476 | G/C | — | uncertain significance |
| rs140031572 | 19:8,808,487 | C/T | — | uncertain significance |
| rs782803809 | 19:8,808,532 | C/T | — | uncertain significance |
| rs782635456 | 19:8,808,558 | A/T | — | uncertain significance |
| rs535368376 | 19:8,808,625 | C/T | — | uncertain significance |
| rs782661274 | 19:8,808,663 | C/A | — | uncertain significance |
| rs781807703 | 19:8,808,733 | C/G | — | uncertain significance |
| rs782679775 | 19:8,808,757 | C/G | — | uncertain significance |
| rs782628590 | 19:8,808,837 | G/C | — | uncertain significance |
| rs782351872 | 19:8,808,939 | G/C | — | uncertain significance |
| rs376440765 | 19:8,808,948 | C/T | — | likely benign |
| rs961197862 | 19:8,808,984 | T/A | — | uncertain significance |
| rs782410923 | 19:8,808,996 | C/T | — | uncertain significance |
| rs2043213890 | 19:8,809,004 | C/A | — | uncertain significance |
| rs782193952 | 19:8,809,005 | T/C | — | uncertain significance |
| rs2512731821 | 19:8,809,030 | A/G | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.