ZNF334
zinc finger protein 334
Summary
This gene encodes a member of the C2H2 zinc finger family. The encoded protein contains a Krueppel-associated box, fourteen C2H2 zinc finger domains, and four C2H2-type/integrase DNA-binding domains. Decreased expression of this gene may be a marker for rheumatoid arthritis. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2516363436 | 20:45,129,953 | C/A | — | uncertain significance |
| rs763384880 | 20:45,129,982 | G/A | — | uncertain significance |
| rs921289341 | 20:45,130,005 | C/A | — | uncertain significance |
| rs769475819 | 20:45,130,051 | G/C | — | uncertain significance |
| rs143648111 | 20:45,130,065 | C/T | — | uncertain significance |
| rs1428737051 | 20:45,130,096 | A/G | — | uncertain significance |
| rs748134496 | 20:45,130,118 | T/A | — | uncertain significance |
| rs146816699 | 20:45,130,122 | C/G | — | uncertain significance |
| rs2516368312 | 20:45,130,149 | C/A | — | uncertain significance |
| rs368938609 | 20:45,130,165 | A/C | — | uncertain significance |
| rs373454002 | 20:45,130,203 | C/T | — | uncertain significance |
| rs775784193 | 20:45,130,252 | C/T | — | uncertain significance |
| rs769146818 | 20:45,130,263 | T/C | — | uncertain significance |
| rs573752780 | 20:45,130,275 | C/T | — | uncertain significance |
| rs142709272 | 20:45,130,295 | G/T | — | uncertain significance |
| rs374488446 | 20:45,130,402 | C/T | — | likely benign |
| rs2516374625 | 20:45,130,434 | T/G | — | uncertain significance |
| rs138011257 | 20:45,130,510 | C/T | — | uncertain significance |
| rs2516378590 | 20:45,130,620 | A/G | — | uncertain significance |
| rs541289992 | 20:45,130,716 | T/C | — | uncertain significance |
| rs1276427668 | 20:45,130,726 | A/T | — | uncertain significance |
| rs151029464 | 20:45,130,797 | G/A | — | uncertain significance |
| rs760237369 | 20:45,130,838 | C/G | — | uncertain significance |
| rs186911997 | 20:45,130,893 | G/A | — | uncertain significance |
| rs201084413 | 20:45,130,962 | T/C | — | uncertain significance |
| rs201701826 | 20:45,130,984 | G/A | — | uncertain significance |
| rs141491794 | 20:45,131,100 | T/C | — | uncertain significance |
| rs368115464 | 20:45,131,133 | C/T | — | uncertain significance |
| rs1389972878 | 20:45,131,230 | A/T | — | uncertain significance |
| rs2516392512 | 20:45,131,311 | T/C | — | uncertain significance |
| rs2061270700 | 20:45,131,314 | C/G | — | uncertain significance |
| rs200631966 | 20:45,131,385 | A/G | — | uncertain significance |
| rs189187102 | 20:45,132,868 | T/G | — | uncertain significance |
| rs766430405 | 20:45,133,259 | A/G | — | uncertain significance |
| rs148860826 | 20:45,133,292 | C/T | — | uncertain significance |
| rs746526118 | 20:45,133,305 | C/A | — | uncertain significance |
| rs847055 | 20:45,142,619 | A/T | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.