GPATCH4
G-patch domain containing 4 (gene/pseudogene)
Summary
Enables RNA binding activity. Predicted to act upstream of or within hematopoietic progenitor cell differentiation. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs886041063 | 1:156,563,752 | — | — | pathogenic |
| rs1677467861 | 1:156,565,084 | T/C | — | uncertain significance |
| rs201712425 | 1:156,565,111 | C/A | — | uncertain significance |
| rs772198575 | 1:156,565,124 | G/C | — | uncertain significance |
| rs760032095 | 1:156,565,171 | G/A | — | uncertain significance |
| rs140797137 | 1:156,565,256 | T/C | — | uncertain significance |
| rs758005641 | 1:156,565,385 | T/A | — | uncertain significance |
| rs77904383 | 1:156,565,386 | T/C | — | likely benign |
| rs1220982084 | 1:156,565,462 | G/A | — | uncertain significance |
| rs746101233 | 1:156,565,521 | G/T | — | uncertain significance |
| rs1279022355 | 1:156,565,522 | C/A | — | uncertain significance |
| rs2526063153 | 1:156,565,524 | C/G | — | uncertain significance |
| rs370560676 | 1:156,565,546 | C/T | — | uncertain significance |
| rs930185688 | 1:156,565,568 | G/A | — | uncertain significance |
| rs2526063868 | 1:156,565,618 | A/T | — | uncertain significance |
| rs1456427043 | 1:156,566,248 | C/G | — | uncertain significance |
| rs138066315 | 1:156,566,366 | G/C | downstream gene variant | — |
| rs190963426 | 1:156,566,431 | C/T | downstream gene variant | — |
| rs557505857 | 1:156,566,595 | C/T | — | — |
| rs3748574 | 1:156,567,778 | A/G | downstream gene variant | — |
| rs150650489 | 1:156,567,863 | A/G | — | likely benign |
| rs773138197 | 1:156,567,894 | C/T | — | uncertain significance |
| rs2526074886 | 1:156,568,027 | T/C | — | uncertain significance |
| rs369352887 | 1:156,568,104 | T/C | — | uncertain significance |
| rs745392006 | 1:156,568,775 | G/A | — | uncertain significance |
| rs771957824 | 1:156,568,776 | C/A | — | uncertain significance |
| rs767697299 | 1:156,571,207 | T/G | — | uncertain significance |
| rs200635908 | 1:156,571,216 | C/G | — | uncertain significance |
| rs369276126 | 1:156,571,221 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.