ICA1L
islet cell autoantigen 1 like
Summary
Predicted to enable protein domain specific binding activity. Predicted to be involved in regulation of transport. Predicted to act upstream of or within spermatid development. Predicted to be located in acrosomal vesicle. Predicted to be active in Golgi apparatus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs72932709 | 2:203,639,501 | A/C | — | — |
| rs62194157 | 2:203,641,142 | T/G | — | — |
| rs62194158 | 2:203,642,155 | G/A | upstream gene variant | — |
| rs775230690 | 2:203,644,300 | G/T | — | uncertain significance |
| rs151227020 | 2:203,644,357 | T/A | — | uncertain significance |
| rs112440397 | 2:203,647,136 | G/T | intron variant | — |
| rs72932727 | 2:203,649,501 | G/C | intron variant | — |
| rs72932729 | 2:203,650,267 | C/T | intron variant | — |
| rs143911965 | 2:203,650,998 | G/A | intron variant | — |
| rs138356872 | 2:203,653,609 | C/T | — | likely benign |
| rs750934313 | 2:203,653,622 | C/T | — | uncertain significance |
| rs1163285685 | 2:203,653,657 | G/A | — | uncertain significance |
| rs774586076 | 2:203,653,709 | C/G | — | uncertain significance |
| rs1475743152 | 2:203,653,783 | A/G | — | uncertain significance |
| rs72932741 | 2:203,661,048 | A/T | intron variant | — |
| rs78128841 | 2:203,663,975 | C/T | intron variant | — |
| rs80087860 | 2:203,673,072 | A/C | intron variant | — |
| rs115400054 | 2:203,676,105 | C/T | intron variant | — |
| rs760799931 | 2:203,676,484 | A/T | — | uncertain significance |
| rs190290860 | 2:203,679,494 | G/A | — | uncertain significance |
| rs148874980 | 2:203,680,638 | A/G | — | uncertain significance |
| rs775359777 | 2:203,680,711 | T/C | — | likely benign |
| rs775001763 | 2:203,680,731 | C/G | — | uncertain significance |
| rs79633844 | 2:203,683,990 | A/G | intron variant | — |
| rs139150386 | 2:203,684,469 | T/A | — | uncertain significance |
| rs369897890 | 2:203,684,596 | C/A | — | uncertain significance |
| rs13011600 | 2:203,684,612 | A/G | — | uncertain significance |
| rs140408869 | 2:203,690,453 | A/G | — | uncertain significance |
| rs1264343627 | 2:203,690,474 | T/C | — | uncertain significance |
| rs758991122 | 2:203,693,606 | C/T | — | uncertain significance |
| rs72932780 | 2:203,695,826 | G/C | intron variant | — |
| rs13017420 | 2:203,701,529 | G/T | — | — |
| rs10207567 | 2:203,714,973 | G/C | intron variant | — |
| rs150622102 | 2:203,716,804 | G/A | — | — |
| rs183979857 | 2:203,723,050 | T/C | intron variant | — |
| rs145664840 | 2:203,726,502 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.