ZC3H11A
zinc finger CCCH-type containing 11A
Summary
Enables RNA binding activity. Involved in poly(A)+ mRNA export from nucleus. Located in transcription export complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7518201 | 1:203,773,096 | A/C | downstream gene variant | — |
| rs34027291 | 1:203,775,522 | C/T | upstream gene variant | — |
| rs2545840944 | 1:203,786,244 | T/C | — | uncertain significance |
| rs12403777 | 1:203,788,756 | T/C | — | — |
| rs1489888562 | 1:203,798,708 | G/T | — | uncertain significance |
| rs2546037256 | 1:203,798,929 | A/T | — | uncertain significance |
| rs761618531 | 1:203,798,946 | A/C | — | uncertain significance |
| rs148052821 | 1:203,798,949 | C/G | — | uncertain significance |
| rs200557789 | 1:203,798,970 | C/A | — | uncertain significance |
| rs375511866 | 1:203,800,809 | A/G | — | uncertain significance |
| rs765761791 | 1:203,800,818 | C/G | — | uncertain significance |
| rs779675915 | 1:203,800,833 | G/A | — | likely benign |
| rs141612045 | 1:203,800,886 | C/A | — | likely benign |
| rs371694128 | 1:203,800,888 | C/G | — | uncertain significance |
| rs747178787 | 1:203,800,891 | C/T | — | uncertain significance |
| rs59867004 | 1:203,801,249 | T/C | downstream gene variant | — |
| rs758839560 | 1:203,802,949 | C/T | — | uncertain significance |
| rs1313293644 | 1:203,807,120 | C/T | — | uncertain significance |
| rs376190579 | 1:203,807,162 | G/A | — | uncertain significance |
| rs760091218 | 1:203,809,499 | A/G | — | likely benign |
| rs1205915069 | 1:203,816,337 | C/G | — | uncertain significance |
| rs1359765327 | 1:203,816,422 | C/A | — | uncertain significance |
| rs1688190854 | 1:203,816,551 | G/A | — | uncertain significance |
| rs747947362 | 1:203,816,576 | T/C | — | likely benign |
| rs147526086 | 1:203,816,657 | C/T | — | uncertain significance |
| rs766895586 | 1:203,816,669 | A/G | — | uncertain significance |
| rs2546326544 | 1:203,816,678 | A/G | — | uncertain significance |
| rs2546326868 | 1:203,816,705 | T/C | — | uncertain significance |
| rs777641508 | 1:203,816,756 | C/T | — | uncertain significance |
| rs201804286 | 1:203,816,767 | G/A | — | uncertain significance |
| rs148859249 | 1:203,816,788 | C/T | — | uncertain significance |
| rs536662986 | 1:203,817,467 | G/A | — | uncertain significance |
| rs374960783 | 1:203,817,489 | G/A | — | likely benign |
| rs146745298 | 1:203,817,527 | G/A | — | uncertain significance |
| rs368114391 | 1:203,818,893 | G/A | — | uncertain significance |
| rs760377233 | 1:203,818,960 | G/A | — | likely benign |
| rs1688840230 | 1:203,818,989 | G/C | — | uncertain significance |
| rs755520271 | 1:203,819,025 | A/C | — | uncertain significance |
| rs1326298378 | 1:203,819,073 | G/A | — | uncertain significance |
| rs202156016 | 1:203,819,098 | G/A | — | uncertain significance |
| rs188389997 | 1:203,819,104 | C/T | — | uncertain significance |
| rs139049200 | 1:203,819,122 | G/C | — | uncertain significance |
| rs769636674 | 1:203,819,152 | A/G | — | uncertain significance |
| rs147577711 | 1:203,819,654 | G/A | — | uncertain significance |
| rs887794553 | 1:203,819,748 | C/A | — | uncertain significance |
| rs2546371040 | 1:203,819,787 | C/T | — | uncertain significance |
| rs528920540 | 1:203,820,200 | G/A | — | uncertain significance |
| rs142870888 | 1:203,821,293 | C/G | — | benign |
| rs778059892 | 1:203,821,313 | C/T | — | uncertain significance |
| rs371361520 | 1:203,821,327 | C/A | — | uncertain significance |
| rs373989899 | 1:203,821,358 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.