ZDHHC1
zDHHC palmitoyltransferase 1
Summary
Enables protein-cysteine S-palmitoyltransferase activity. Involved in antiviral innate immune response; protein palmitoylation; and regulation of defense response. Located in Golgi apparatus and endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs939722581 | 16:67,428,607 | G/A | — | uncertain significance |
| rs1431388890 | 16:67,428,615 | T/A | — | uncertain significance |
| rs1036905545 | 16:67,428,616 | C/T | — | uncertain significance |
| rs1047983678 | 16:67,428,625 | C/G | — | uncertain significance |
| rs1363084327 | 16:67,428,636 | G/A | — | uncertain significance |
| rs757492652 | 16:67,428,766 | G/A | — | uncertain significance |
| rs1328207028 | 16:67,428,793 | G/C | — | uncertain significance |
| rs749577256 | 16:67,428,796 | C/T | — | uncertain significance |
| rs769869424 | 16:67,428,913 | G/A | — | uncertain significance |
| rs775505887 | 16:67,428,921 | G/A | — | uncertain significance |
| rs2040395727 | 16:67,428,922 | G/A | — | uncertain significance |
| rs766875350 | 16:67,428,978 | G/A | — | likely benign |
| rs374630307 | 16:67,429,014 | A/G | — | uncertain significance |
| rs559342411 | 16:67,429,038 | T/G | — | uncertain significance |
| rs765414079 | 16:67,429,057 | C/T | — | uncertain significance |
| rs575267844 | 16:67,429,087 | T/A | — | uncertain significance |
| rs143510690 | 16:67,429,390 | G/A | — | uncertain significance |
| rs145809493 | 16:67,432,125 | C/T | — | uncertain significance |
| rs1325301901 | 16:67,432,172 | C/A | — | uncertain significance |
| rs1435633500 | 16:67,432,179 | G/T | — | uncertain significance |
| rs762668418 | 16:67,432,185 | C/T | — | uncertain significance |
| rs2508523137 | 16:67,432,515 | C/T | — | uncertain significance |
| rs2508523400 | 16:67,432,547 | G/A | — | uncertain significance |
| rs150452234 | 16:67,432,584 | C/T | — | uncertain significance |
| rs889715739 | 16:67,432,590 | C/T | — | uncertain significance |
| rs1180578774 | 16:67,432,737 | T/C | — | uncertain significance |
| rs756237481 | 16:67,432,743 | C/T | — | uncertain significance |
| rs779123839 | 16:67,432,753 | T/A | — | uncertain significance |
| rs774844883 | 16:67,432,775 | G/A | — | likely benign |
| rs2508525618 | 16:67,432,789 | C/G | — | uncertain significance |
| rs775473492 | 16:67,434,920 | T/A | — | uncertain significance |
| rs775157699 | 16:67,434,960 | C/T | — | uncertain significance |
| rs774105548 | 16:67,434,975 | G/C | — | uncertain significance |
| rs375208273 | 16:67,434,978 | C/T | — | uncertain significance |
| rs199651286 | 16:67,434,990 | C/T | — | uncertain significance |
| rs2508556788 | 16:67,440,107 | T/C | — | uncertain significance |
| rs114187593 | 16:67,440,205 | C/T | — | benign |
| rs781144632 | 16:67,440,284 | G/A | — | uncertain significance |
| rs376044283 | 16:67,440,285 | G/A | — | uncertain significance |
| rs2508558448 | 16:67,440,299 | C/T | — | uncertain significance |
| rs117903946 | 16:67,449,639 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.