RCOR2
REST corepressor 2
Summary
Predicted to enable transcription corepressor activity. Predicted to be involved in negative regulation of DNA-templated transcription and regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. Predicted to be part of histone deacetylase complex and transcription regulator complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs750159142 | 11:63,679,392 | T/G | — | uncertain significance |
| rs913201485 | 11:63,679,405 | G/C | — | uncertain significance |
| rs2539358724 | 11:63,679,407 | G/A | — | uncertain significance |
| rs565254520 | 11:63,679,449 | G/A | — | uncertain significance |
| rs1277791369 | 11:63,679,524 | G/T | — | uncertain significance |
| rs774946706 | 11:63,679,557 | G/A | — | uncertain significance |
| rs548233693 | 11:63,679,617 | C/T | — | uncertain significance |
| rs1179884901 | 11:63,679,618 | G/C | — | uncertain significance |
| rs2539359826 | 11:63,679,802 | G/A | — | uncertain significance |
| rs2539359938 | 11:63,679,881 | C/T | — | uncertain significance |
| rs1476311673 | 11:63,680,412 | C/T | — | uncertain significance |
| rs4980532 | 11:63,680,719 | C/T | downstream gene variant | — |
| rs1276485780 | 11:63,681,575 | A/G | — | uncertain significance |
| rs758917942 | 11:63,681,614 | G/A | — | uncertain significance |
| rs371327834 | 11:63,681,756 | C/G | — | uncertain significance |
| rs199984646 | 11:63,681,782 | C/T | — | uncertain significance |
| rs762273099 | 11:63,681,783 | G/C | — | uncertain significance |
| rs2539363910 | 11:63,681,953 | T/C | — | uncertain significance |
| rs377722799 | 11:63,681,981 | T/G | — | uncertain significance |
| rs767244177 | 11:63,682,170 | G/C | — | uncertain significance |
| rs146976071 | 11:63,682,244 | C/T | synonymous variant | — |
| rs114566006 | 11:63,682,296 | G/A | — | benign |
| rs981994837 | 11:63,682,673 | T/C | — | uncertain significance |
| rs1941839518 | 11:63,682,724 | G/A | — | uncertain significance |
| rs1034054539 | 11:63,683,081 | T/G | — | uncertain significance |
| rs754458985 | 11:63,683,841 | G/A | — | uncertain significance |
| rs2539367613 | 11:63,683,861 | A/G | — | likely benign |
| rs372768915 | 11:63,683,889 | T/A | — | uncertain significance |
| rs1479842879 | 11:63,683,891 | C/G | — | uncertain significance |
| rs772745604 | 11:63,683,907 | G/C | — | uncertain significance |
| rs149337452 | 11:63,683,958 | G/A | regulatory region variant | — |
| rs76370995 | 11:63,685,804 | G/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.