TOX2
TOX high mobility group box family member 2
Summary
Enables transcription coactivator activity. Involved in positive regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs984748166 | 20:42,543,550 | C/T | — | uncertain significance |
| rs909809329 | 20:42,543,556 | G/T | — | uncertain significance |
| rs6073257 | 20:42,561,422 | C/T | intron variant | — |
| rs6031252 | 20:42,573,822 | C/A | intron variant | — |
| rs201938708 | 20:42,602,008 | T/C | — | uncertain significance |
| rs138829322 | 20:42,602,019 | A/G | — | uncertain significance |
| rs755427969 | 20:42,602,064 | A/G | — | uncertain significance |
| rs369949490 | 20:42,635,254 | C/T | — | uncertain significance |
| rs368247726 | 20:42,635,328 | G/A | — | uncertain significance |
| rs2515592055 | 20:42,635,407 | A/G | — | uncertain significance |
| rs1254464852 | 20:42,635,430 | A/G | — | uncertain significance |
| rs6031303 | 20:42,657,325 | A/T | — | — |
| rs6017247 | 20:42,657,841 | T/C | regulatory region variant | — |
| rs6031305 | 20:42,658,083 | A/G | regulatory region variant | — |
| rs6103575 | 20:42,658,613 | C/A | — | — |
| rs6073290 | 20:42,658,759 | A/G | intron variant | — |
| rs6017249 | 20:42,660,436 | A/T | intron variant | — |
| rs183623967 | 20:42,677,758 | C/T | intron variant | — |
| rs6103583 | 20:42,678,242 | G/A | intron variant | — |
| rs41279272 | 20:42,679,955 | A/G | — | likely benign |
| rs754794148 | 20:42,680,063 | A/T | — | uncertain significance |
| rs540374188 | 20:42,680,074 | G/A | — | uncertain significance |
| rs368511505 | 20:42,680,078 | A/G | — | uncertain significance |
| rs184778931 | 20:42,680,081 | C/T | — | uncertain significance |
| rs376494319 | 20:42,680,082 | G/A | — | uncertain significance |
| rs561015693 | 20:42,682,943 | C/T | — | uncertain significance |
| rs1569140429 | 20:42,682,953 | G/T | — | uncertain significance |
| rs138123229 | 20:42,682,957 | C/T | — | uncertain significance |
| rs867839104 | 20:42,682,997 | A/G | — | uncertain significance |
| rs1462680382 | 20:42,683,113 | G/A | — | uncertain significance |
| rs1216489112 | 20:42,694,436 | A/C | — | uncertain significance |
| rs2071804592 | 20:42,694,437 | T/C | — | uncertain significance |
| rs374248829 | 20:42,694,464 | C/T | — | uncertain significance |
| rs770444785 | 20:42,694,514 | C/T | — | uncertain significance |
| rs1031249099 | 20:42,694,530 | A/T | — | uncertain significance |
| rs748284007 | 20:42,694,566 | C/T | — | uncertain significance |
| rs749650557 | 20:42,694,581 | C/T | — | uncertain significance |
| rs143798869 | 20:42,694,619 | C/T | — | uncertain significance |
| rs778012248 | 20:42,694,646 | C/A | — | uncertain significance |
| rs755688390 | 20:42,695,440 | G/T | — | uncertain significance |
| rs2515698908 | 20:42,695,442 | A/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.