L3MBTL4
L3MBTL histone methyl-lysine binding protein 4
Summary
Predicted to enable chromatin binding activity and histone binding activity. Predicted to be involved in negative regulation of DNA-templated transcription. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs184790196 | 18:5,956,224 | C/T | — | uncertain significance |
| rs1442762350 | 18:5,956,245 | C/T | — | uncertain significance |
| rs2144576678 | 18:5,956,263 | G/A | — | uncertain significance |
| rs2095226847 | 18:5,956,370 | G/A | — | uncertain significance |
| rs2155579 | 18:5,959,006 | A/C | intron variant | — |
| rs715149 | 18:5,962,067 | T/A | — | — |
| rs373197727 | 18:5,969,472 | C/A | — | uncertain significance |
| rs765233692 | 18:5,969,481 | G/C | — | uncertain significance |
| rs373941763 | 18:5,969,507 | G/A | — | uncertain significance |
| rs767710721 | 18:5,969,537 | T/C | — | uncertain significance |
| rs1539808 | 18:5,978,931 | C/T | intron variant | — |
| rs138175239 | 18:6,080,903 | A/G | — | uncertain significance |
| rs372111918 | 18:6,093,387 | T/C | — | uncertain significance |
| rs369119792 | 18:6,093,472 | C/T | — | uncertain significance |
| rs372472030 | 18:6,138,211 | C/T | — | uncertain significance |
| rs2511245676 | 18:6,138,226 | T/C | — | uncertain significance |
| rs1489488386 | 18:6,138,233 | T/C | — | uncertain significance |
| rs202192251 | 18:6,138,275 | G/T | — | uncertain significance |
| rs1177518531 | 18:6,138,280 | T/G | — | uncertain significance |
| rs537938132 | 18:6,138,785 | A/C | — | — |
| rs369477616 | 18:6,171,870 | G/C | — | uncertain significance |
| rs2511847775 | 18:6,213,163 | A/C | — | uncertain significance |
| rs138372104 | 18:6,213,174 | C/T | — | likely benign |
| rs374471908 | 18:6,213,230 | A/G | — | uncertain significance |
| rs139480207 | 18:6,215,816 | T/A | — | uncertain significance |
| rs773056707 | 18:6,215,834 | C/T | — | uncertain significance |
| rs370912442 | 18:6,239,780 | G/A | — | uncertain significance |
| rs1369772189 | 18:6,239,782 | T/C | — | uncertain significance |
| rs769707553 | 18:6,239,790 | C/A | — | uncertain significance |
| rs1397679607 | 18:6,239,809 | G/T | — | uncertain significance |
| rs199523434 | 18:6,239,823 | C/T | — | uncertain significance |
| rs147627432 | 18:6,241,358 | G/A | — | uncertain significance |
| rs757539125 | 18:6,241,407 | C/A | — | uncertain significance |
| rs377614549 | 18:6,243,294 | C/G | — | uncertain significance |
| rs780230270 | 18:6,243,335 | C/T | — | uncertain significance |
| rs908386779 | 18:6,243,349 | T/C | — | uncertain significance |
| rs371265301 | 18:6,243,379 | T/C | — | uncertain significance |
| rs140374046 | 18:6,244,503 | A/T | — | uncertain significance |
| rs752700059 | 18:6,244,540 | T/G | — | uncertain significance |
| rs2512343193 | 18:6,263,977 | G/A | — | uncertain significance |
| rs201234226 | 18:6,264,014 | C/A | — | uncertain significance |
| rs2048522055 | 18:6,264,017 | C/T | — | uncertain significance |
| rs1461941448 | 18:6,301,926 | C/T | — | uncertain significance |
| rs377411728 | 18:6,305,754 | C/T | — | — |
| rs8097200 | 18:6,309,334 | A/T | — | — |
| rs777141155 | 18:6,311,561 | C/T | — | uncertain significance |
| rs11660658 | 18:6,410,213 | T/C | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.