UNK
unk zinc finger
Summary
Enables mRNA CDS binding activity. Involved in cell morphogenesis involved in neuron differentiation and negative regulation of cytoplasmic translation. Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs78057960 | 17:73,779,075 | C/A | — | — |
| rs1474409133 | 17:73,781,064 | A/C | — | uncertain significance |
| rs4789229 | 17:73,796,002 | C/G | — | — |
| rs11652539 | 17:73,797,775 | C/A | intron variant | — |
| rs10401030 | 17:73,799,103 | A/G | — | — |
| rs139729499 | 17:73,805,868 | G/T | — | uncertain significance |
| rs201905047 | 17:73,805,945 | G/A | — | uncertain significance |
| rs139675007 | 17:73,808,761 | C/T | regulatory region variant | — |
| rs1264339563 | 17:73,809,270 | G/A | — | uncertain significance |
| rs1005314489 | 17:73,809,892 | G/C | — | uncertain significance |
| rs199569572 | 17:73,809,906 | G/A | — | uncertain significance |
| rs11658385 | 17:73,810,400 | C/T | downstream gene variant | — |
| rs9913385 | 17:73,810,674 | C/A | downstream gene variant | — |
| rs35103294 | 17:73,810,937 | C/T | regulatory region variant | — |
| rs2143796334 | 17:73,811,334 | C/T | — | uncertain significance |
| rs113930559 | 17:73,813,398 | T/C | — | benign |
| rs754393636 | 17:73,813,432 | G/C | — | uncertain significance |
| rs763366409 | 17:73,813,515 | T/C | — | uncertain significance |
| rs2545956722 | 17:73,814,227 | A/G | — | uncertain significance |
| rs76256594 | 17:73,814,836 | C/T | — | benign |
| rs373411446 | 17:73,814,852 | G/A | — | uncertain significance |
| rs552908426 | 17:73,815,803 | G/A | — | uncertain significance |
| rs2062053567 | 17:73,816,183 | T/C | — | uncertain significance |
| rs2545967062 | 17:73,819,356 | C/T | — | uncertain significance |
| rs2143835645 | 17:73,819,382 | G/A | — | uncertain significance |
| rs768235083 | 17:73,819,398 | C/T | — | uncertain significance |
| rs2062086520 | 17:73,819,404 | G/A | — | uncertain significance |
| rs774346420 | 17:73,819,409 | G/A | — | uncertain significance |
| rs765398377 | 17:73,819,424 | C/T | — | uncertain significance |
| rs2545967528 | 17:73,819,505 | C/A | — | uncertain significance |
| rs541391429 | 17:73,819,508 | G/A | — | uncertain significance |
| rs561355053 | 17:73,819,509 | C/A | — | uncertain significance |
| rs573819589 | 17:73,819,517 | G/A | — | likely benign |
| rs531397930 | 17:73,819,578 | G/A | — | uncertain significance |
| rs372706399 | 17:73,820,362 | C/T | — | uncertain significance |
| rs575612726 | 17:73,820,374 | T/G | — | uncertain significance |
| rs757873524 | 17:73,820,451 | G/A | — | uncertain significance |
| rs772068812 | 17:73,820,494 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.