LCOR
ligand dependent nuclear receptor corepressor
Summary
LCOR is a transcriptional corepressor widely expressed in fetal and adult tissues that is recruited to agonist-bound nuclear receptors through a single LxxLL motif, also referred to as a nuclear receptor (NR) box (Fernandes et al., 2003 [PubMed 12535528]).[supplied by OMIM, Mar 2008]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs12258469 | 10:98,639,434 | C/T | intron variant | — |
| rs17112190 | 10:98,639,846 | G/A | intron variant | — |
| rs7906294 | 10:98,697,842 | C/G | intron variant | — |
| rs2492964555 | 10:98,708,981 | T/C | — | uncertain significance |
| rs1847691645 | 10:98,711,911 | C/A | — | uncertain significance |
| rs148761756 | 10:98,714,886 | C/T | — | uncertain significance |
| rs763593857 | 10:98,714,937 | T/C | — | uncertain significance |
| rs913165449 | 10:98,715,051 | C/T | — | uncertain significance |
| rs2492977665 | 10:98,715,087 | C/G | — | uncertain significance |
| rs200583240 | 10:98,715,216 | T/C | — | uncertain significance |
| rs145573126 | 10:98,715,228 | C/T | — | uncertain significance |
| rs1037672122 | 10:98,715,245 | A/C | — | uncertain significance |
| rs78929926 | 10:98,715,284 | A/G | — | uncertain significance |
| rs773041729 | 10:98,715,294 | A/G | — | uncertain significance |
| rs889205142 | 10:98,715,333 | C/T | — | uncertain significance |
| rs1163920471 | 10:98,715,375 | A/G | — | uncertain significance |
| rs2492979270 | 10:98,715,608 | G/A | — | uncertain significance |
| rs2492979378 | 10:98,715,645 | C/G | — | uncertain significance |
| rs186552055 | 10:98,730,145 | C/T | intron variant | — |
| rs11188980 | 10:98,741,293 | A/T | missense variant | — |
| rs1160269548 | 10:98,741,655 | A/G | — | uncertain significance |
| rs1293062296 | 10:98,742,000 | C/T | — | uncertain significance |
| rs149783917 | 10:98,742,525 | A/G | — | uncertain significance |
| rs746615879 | 10:98,742,781 | G/A | — | uncertain significance |
| rs768983264 | 10:98,743,028 | T/G | — | likely benign |
| rs1848112312 | 10:98,743,129 | A/C | — | uncertain significance |
| rs779904619 | 10:98,744,089 | A/G | — | uncertain significance |
| rs193262451 | 10:98,744,167 | G/A | — | uncertain significance |
| rs2493027056 | 10:98,744,388 | C/A | — | uncertain significance |
| rs763723577 | 10:98,744,461 | C/A | — | uncertain significance |
| rs746854067 | 10:98,744,671 | C/T | — | uncertain significance |
| rs2493028126 | 10:98,744,764 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.