ZGPAT
zinc finger CCCH-type and G-patch domain containing
Summary
Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of epidermal growth factor-activated receptor activity and negative regulation of transcription by RNA polymerase II. Located in nucleoplasm and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants64 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs145783963 | 20:62,339,942 | G/A | — | uncertain significance |
| rs779358644 | 20:62,339,946 | G/C | — | uncertain significance |
| rs2517415469 | 20:62,339,993 | G/A | — | uncertain significance |
| rs1379599118 | 20:62,340,117 | T/C | — | uncertain significance |
| rs2517416727 | 20:62,340,155 | G/A | — | uncertain significance |
| rs374989957 | 20:62,340,221 | C/G | — | uncertain significance |
| rs6089764 | 20:62,340,246 | C/T | — | uncertain significance |
| rs1601309740 | 20:62,340,326 | A/T | — | uncertain significance |
| rs2517418677 | 20:62,340,366 | T/A | — | uncertain significance |
| rs771287246 | 20:62,340,419 | G/T | — | uncertain significance |
| rs764405178 | 20:62,340,440 | C/G | — | uncertain significance |
| rs769165453 | 20:62,340,497 | C/T | — | uncertain significance |
| rs3761123 | 20:62,342,468 | G/T | — | — |
| rs2750482 | 20:62,343,164 | T/A | — | — |
| rs2315008 | 20:62,343,956 | T/G | upstream gene variant | — |
| rs2315009 | 20:62,344,140 | C/T | — | — |
| rs143155137 | 20:62,345,183 | A/G | intron variant | — |
| rs62217798 | 20:62,347,189 | G/C | — | — |
| rs62217799 | 20:62,347,191 | G/T | — | — |
| rs4809327 | 20:62,348,190 | C/G | — | — |
| rs4809328 | 20:62,348,327 | C/T | intron variant | — |
| rs4809329 | 20:62,348,460 | C/T | intron variant | — |
| rs6062504 | 20:62,348,907 | A/T | — | — |
| rs4809330 | 20:62,349,586 | A/C | — | — |
| rs2738759 | 20:62,350,413 | A/C | — | — |
| rs6062304 | 20:62,351,539 | A/T | intron variant | — |
| rs183850545 | 20:62,353,818 | C/T | intron variant | — |
| rs1758205 | 20:62,355,756 | G/T | — | — |
| rs187577818 | 20:62,358,869 | A/C | regulatory region variant | — |
| rs2427531 | 20:62,362,116 | G/C | regulatory region variant | — |
| rs6062509 | 20:62,362,563 | G/T | regulatory region variant | — |
| rs71325463 | 20:62,362,834 | G/A | regulatory region variant | — |
| rs112756706 | 20:62,362,850 | A/T | regulatory region variant | — |
| rs6122157 | 20:62,362,954 | G/A | — | — |
| rs2427532 | 20:62,363,817 | G/C | — | — |
| rs539428117 | 20:62,363,837 | G/A | — | — |
| rs55791529 | 20:62,363,858 | C/A | — | — |
| rs2517478810 | 20:62,364,623 | C/T | — | uncertain significance |
| rs374721226 | 20:62,364,647 | G/A | — | uncertain significance |
| rs776481460 | 20:62,364,689 | G/A | — | uncertain significance |
| rs533220710 | 20:62,364,973 | C/A | — | uncertain significance |
| rs200749334 | 20:62,365,028 | C/T | — | uncertain significance |
| rs747760596 | 20:62,365,049 | G/A | — | uncertain significance |
| rs1265968613 | 20:62,365,083 | A/G | — | uncertain significance |
| rs1176701629 | 20:62,366,011 | G/A | — | uncertain significance |
| rs2517485148 | 20:62,366,087 | C/A | — | uncertain significance |
| rs2517485197 | 20:62,366,095 | T/C | — | uncertain significance |
| rs370604942 | 20:62,366,643 | C/T | — | uncertain significance |
| rs766390404 | 20:62,366,650 | G/T | — | uncertain significance |
| rs751698813 | 20:62,366,651 | T/A | — | uncertain significance |
| rs200343535 | 20:62,366,681 | C/T | — | uncertain significance |
| rs576313585 | 20:62,366,697 | A/G | — | likely benign |
| rs767662975 | 20:62,366,733 | A/C | — | uncertain significance |
| rs1354933283 | 20:62,366,748 | T/C | — | likely benign |
| rs201928593 | 20:62,366,765 | C/T | — | uncertain significance |
| rs2517488729 | 20:62,366,827 | C/G | — | uncertain significance |
| rs368346804 | 20:62,366,909 | G/A | — | likely benign |
| rs767605942 | 20:62,367,137 | A/T | — | uncertain significance |
| rs1456208482 | 20:62,367,144 | C/T | — | uncertain significance |
| rs1356299990 | 20:62,367,177 | C/T | — | uncertain significance |
| rs750664509 | 20:62,367,200 | C/T | — | uncertain significance |
| rs369758532 | 20:62,367,201 | G/A | — | uncertain significance |
| rs946269173 | 20:62,367,212 | G/T | — | uncertain significance |
| rs2517491144 | 20:62,367,213 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.