ZNF488
zinc finger protein 488
Summary
Predicted to enable DNA binding activity and zinc ion binding activity. Predicted to be involved in oligodendrocyte development and regulation of DNA-templated transcription. Predicted to act upstream of or within negative regulation of DNA-templated transcription and positive regulation of oligodendrocyte differentiation. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants24 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs187111258 | 10:48,354,315 | A/G | regulatory region variant | — |
| rs140874855 | 10:48,370,567 | C/T | — | uncertain significance |
| rs199801715 | 10:48,370,618 | C/T | — | uncertain significance |
| rs547062492 | 10:48,370,660 | G/A | — | uncertain significance |
| rs771854712 | 10:48,370,665 | T/C | — | likely benign |
| rs374041008 | 10:48,370,696 | G/A | — | likely benign |
| rs78212329 | 10:48,370,726 | C/T | — | uncertain significance |
| rs140711392 | 10:48,370,795 | C/T | — | uncertain significance |
| rs372710742 | 10:48,370,856 | G/A | — | uncertain significance |
| rs552091559 | 10:48,370,863 | C/G | — | uncertain significance |
| rs2549038240 | 10:48,370,896 | C/T | — | uncertain significance |
| rs782483934 | 10:48,370,902 | G/T | — | uncertain significance |
| rs782602245 | 10:48,371,032 | C/T | — | uncertain significance |
| rs150285927 | 10:48,371,038 | G/A | — | uncertain significance |
| rs781796487 | 10:48,371,115 | C/T | — | uncertain significance |
| rs373095491 | 10:48,371,163 | A/G | — | uncertain significance |
| rs782596702 | 10:48,371,226 | A/G | — | likely benign |
| rs201359415 | 10:48,371,248 | T/A | — | uncertain significance |
| rs781893966 | 10:48,371,289 | T/G | — | uncertain significance |
| rs150817564 | 10:48,371,325 | A/G | — | uncertain significance |
| rs139262307 | 10:48,371,341 | G/T | — | uncertain significance |
| rs200628899 | 10:48,371,392 | C/T | — | uncertain significance |
| rs146850128 | 10:48,371,467 | G/A | — | likely benign |
| rs201761137 | 10:48,371,511 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.