GON4L
gon-4 like
Summary
Predicted to enable transcription corepressor activity. Predicted to be involved in negative regulation of DNA-templated transcription. Predicted to act upstream of or within B cell differentiation. Located in nuclear body. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11264409 | 1:155,715,641 | G/A | regulatory region variant | — |
| rs766347337 | 1:155,721,550 | G/A | — | likely benign |
| rs1219408000 | 1:155,721,939 | A/G | — | likely benign |
| rs1756236 | 1:155,721,974 | G/T | — | likely benign |
| rs745365801 | 1:155,722,089 | C/T | — | likely benign |
| rs892180288 | 1:155,722,092 | G/A | — | likely benign |
| rs528896667 | 1:155,722,182 | C/T | — | likely benign |
| rs755943779 | 1:155,723,004 | G/T | — | uncertain significance |
| rs7550402 | 1:155,724,898 | T/G | — | — |
| rs541961794 | 1:155,727,894 | G/A | — | — |
| rs150685211 | 1:155,732,175 | C/G | — | benign |
| rs1350509021 | 1:155,733,185 | T/C | — | likely benign |
| rs607834 | 1:155,733,257 | T/G | — | likely benign |
| rs72706143 | 1:155,733,358 | G/A | — | likely benign |
| rs559465299 | 1:155,735,148 | C/T | — | likely benign |
| rs677219 | 1:155,735,721 | A/G | — | likely benign |
| rs150057388 | 1:155,735,790 | G/A | — | benign |
| rs141121842 | 1:155,735,887 | T/G | — | likely benign |
| rs144768837 | 1:155,735,988 | G/C | — | likely benign |
| rs185584587 | 1:155,736,041 | C/T | — | likely benign |
| rs61745601 | 1:155,736,258 | C/T | — | likely benign |
| rs534559107 | 1:155,738,015 | A/C | — | — |
| rs143886196 | 1:155,741,005 | C/T | — | likely benign |
| rs1553200563 | 1:155,742,897 | T/C | — | uncertain significance |
| rs146504521 | 1:155,746,245 | G/C | — | likely benign |
| rs143202491 | 1:155,747,464 | A/G | — | likely benign |
| rs2985707 | 1:155,749,870 | G/A | intron variant | — |
| rs200801519 | 1:155,774,873 | A/G | — | likely benign |
| rs71628688 | 1:155,779,031 | G/A | — | — |
| rs193114838 | 1:155,779,640 | A/C | intron variant | — |
| rs368634028 | 1:155,783,530 | C/T | — | likely benign |
| rs72706172 | 1:155,797,492 | A/G | — | — |
| rs140893634 | 1:155,803,205 | C/T | intron variant | — |
| rs147220372 | 1:155,823,496 | C/T | — | likely benign |
| rs775734366 | 1:155,823,498 | T/C | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.