STXBP3
syntaxin binding protein 3
Summary
Enables syntaxin binding activity. Involved in negative regulation of calcium ion-dependent exocytosis; neutrophil degranulation; and platelet aggregation. Located in cytosol; plasma membrane; and secretory granule. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1261197120 | 1:109,299,336 | G/A | — | uncertain significance |
| rs1662066309 | 1:109,301,178 | A/G | — | uncertain significance |
| rs753442306 | 1:109,302,657 | A/G | — | uncertain significance |
| rs141377350 | 1:109,302,697 | A/G | — | uncertain significance |
| rs115292790 | 1:109,310,728 | G/A | upstream gene variant | — |
| rs2524492978 | 1:109,315,290 | T/C | — | uncertain significance |
| rs145246178 | 1:109,315,291 | A/T | — | uncertain significance |
| rs377217237 | 1:109,315,383 | G/A | — | likely benign |
| rs2524493221 | 1:109,315,388 | G/T | — | uncertain significance |
| rs771177543 | 1:109,315,420 | A/G | — | uncertain significance |
| rs1036637188 | 1:109,318,969 | A/G | — | uncertain significance |
| rs2524500585 | 1:109,318,983 | G/A | — | likely pathogenic |
| rs2524504904 | 1:109,321,921 | C/T | — | uncertain significance |
| rs199558647 | 1:109,325,055 | A/G | — | uncertain significance |
| rs746585106 | 1:109,325,278 | C/T | — | uncertain significance |
| rs375222072 | 1:109,336,249 | T/G | — | uncertain significance |
| rs147446724 | 1:109,336,253 | G/A | — | uncertain significance |
| rs1384737521 | 1:109,336,270 | G/A | — | uncertain significance |
| rs2524537325 | 1:109,336,271 | T/G | — | likely pathogenic |
| rs768181860 | 1:109,337,489 | A/C | — | uncertain significance |
| rs1219042264 | 1:109,337,494 | A/C | — | uncertain significance |
| rs772306065 | 1:109,338,901 | T/A | — | uncertain significance |
| rs145367060 | 1:109,339,298 | A/G | — | uncertain significance |
| rs757694612 | 1:109,340,816 | T/G | — | uncertain significance |
| rs1416472478 | 1:109,340,830 | T/G | — | uncertain significance |
| rs140703879 | 1:109,345,776 | T/C | intron variant | — |
| rs757268104 | 1:109,350,066 | A/C | — | uncertain significance |
| rs143767674 | 1:109,350,067 | A/G | — | uncertain significance |
| rs917624374 | 1:109,351,429 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.