STXBP4
syntaxin binding protein 4
Summary
Enables syntaxin binding activity. Involved in several processes, including positive regulation of cell cycle G1/S phase transition; positive regulation of keratinocyte proliferation; and protein stabilization. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6504950 | 17:53,056,471 | G/A | intron variant | — |
| rs1445120718 | 17:53,068,186 | G/T | — | uncertain significance |
| rs765530887 | 17:53,068,204 | G/T | — | uncertain significance |
| rs372904801 | 17:53,068,211 | A/G | — | likely benign |
| rs757140831 | 17:53,068,259 | C/T | — | uncertain significance |
| rs778811461 | 17:53,068,260 | G/A | — | uncertain significance |
| rs769987070 | 17:53,076,712 | C/G | — | uncertain significance |
| rs200471337 | 17:53,076,713 | G/A | — | uncertain significance |
| rs2509542808 | 17:53,076,734 | T/G | — | uncertain significance |
| rs750031690 | 17:53,076,769 | T/C | — | uncertain significance |
| rs1156287 | 17:53,076,799 | G/A | missense variant | — |
| rs1223223320 | 17:53,077,112 | C/T | — | uncertain significance |
| rs1480428015 | 17:53,077,199 | G/T | — | likely benign |
| rs140691664 | 17:53,084,867 | A/C | — | uncertain significance |
| rs2078032824 | 17:53,084,927 | C/T | — | uncertain significance |
| rs113592246 | 17:53,096,179 | G/A | intron variant | — |
| rs78781855 | 17:53,102,367 | T/G | intron variant | — |
| rs2078503594 | 17:53,108,553 | C/A | — | uncertain significance |
| rs2509640487 | 17:53,108,600 | C/G | — | uncertain significance |
| rs62078811 | 17:53,109,176 | G/A | intron variant | — |
| rs57785146 | 17:53,112,192 | G/A | intron variant | — |
| rs2509689782 | 17:53,124,510 | A/G | — | uncertain significance |
| rs60940178 | 17:53,147,725 | G/T | — | — |
| rs770185487 | 17:53,150,373 | G/A | — | uncertain significance |
| rs767763765 | 17:53,150,405 | G/C | — | uncertain significance |
| rs974439618 | 17:53,150,412 | T/C | — | uncertain significance |
| rs866011823 | 17:53,155,469 | A/G | — | uncertain significance |
| rs777780406 | 17:53,155,478 | G/A | — | uncertain significance |
| rs953103086 | 17:53,158,464 | A/G | — | uncertain significance |
| rs765126157 | 17:53,158,539 | T/C | — | uncertain significance |
| rs35505893 | 17:53,162,486 | G/C | — | — |
| rs2787487 | 17:53,209,382 | G/C | intron variant | — |
| rs2787486 | 17:53,209,774 | A/T | — | — |
| rs2628317 | 17:53,212,573 | A/G | intron variant | — |
| rs2509863530 | 17:53,218,671 | G/T | — | uncertain significance |
| rs1485718070 | 17:53,218,698 | A/G | — | uncertain significance |
| rs374843138 | 17:53,237,165 | A/T | — | uncertain significance |
| rs2529518 | 17:53,252,010 | C/T | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.