SYT9
synaptotagmin 9
Summary
Predicted to enable SNARE binding activity; calcium ion sensor activity; and calcium-dependent phospholipid binding activity. Predicted to be involved in chemical synaptic transmission; regulation of vesicle-mediated transport; and vesicle-mediated transport. Predicted to be located in clathrin-coated endocytic vesicle membrane. Predicted to be active in hippocampal mossy fiber to CA3 synapse; plasma membrane; and secretory vesicle. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs747985314 | 11:7,273,427 | G/A | — | uncertain significance |
| rs749543472 | 11:7,273,467 | C/T | — | uncertain significance |
| rs146068689 | 11:7,273,526 | C/G | — | uncertain significance |
| rs765977411 | 11:7,324,273 | T/C | — | uncertain significance |
| rs982227091 | 11:7,324,341 | G/A | — | uncertain significance |
| rs778837379 | 11:7,324,426 | A/G | — | uncertain significance |
| rs1467974321 | 11:7,324,443 | A/G | — | uncertain significance |
| rs148454232 | 11:7,324,463 | G/C | — | uncertain significance |
| rs1054802519 | 11:7,324,467 | T/C | — | uncertain significance |
| rs779476138 | 11:7,324,578 | G/A | — | likely benign |
| rs202241519 | 11:7,324,581 | C/T | — | uncertain significance |
| rs754383902 | 11:7,334,692 | A/C | — | uncertain significance |
| rs568579361 | 11:7,334,765 | G/A | — | uncertain significance |
| rs753974212 | 11:7,334,772 | G/A | — | likely benign |
| rs138467146 | 11:7,334,930 | C/T | — | uncertain significance |
| rs1376647871 | 11:7,334,975 | C/G | — | uncertain significance |
| rs202199041 | 11:7,335,072 | G/A | — | uncertain significance |
| rs10769780 | 11:7,367,095 | T/A | — | — |
| rs144728371 | 11:7,372,714 | G/T | — | — |
| rs10769783 | 11:7,396,191 | A/T | — | — |
| rs72846013 | 11:7,408,743 | G/A | intron variant | — |
| rs1420453158 | 11:7,437,291 | G/A | — | uncertain significance |
| rs1847242090 | 11:7,437,345 | A/G | — | uncertain significance |
| rs369237179 | 11:7,439,324 | A/T | — | uncertain significance |
| rs776629146 | 11:7,439,358 | C/T | — | uncertain significance |
| rs571404172 | 11:7,441,738 | G/A | — | uncertain significance |
| rs772941356 | 11:7,441,750 | G/A | — | uncertain significance |
| rs2494294495 | 11:7,441,805 | A/T | — | uncertain significance |
| rs200921056 | 11:7,441,831 | C/T | — | uncertain significance |
| rs796805386 | 11:7,441,861 | G/C | — | uncertain significance |
| rs10839780 | 11:7,446,728 | G/T | downstream gene variant | — |
| rs5001115 | 11:7,457,481 | A/T | — | — |
| rs4076555 | 11:7,464,372 | T/C | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.