NCLN
nicalin
Summary
Enables ribosome binding activity. Involved in several processes, including multi-pass transmembrane protein insertion into ER membrane; protein stabilization; and regulation of protein complex stability. Located in endoplasmic reticulum membrane. Part of multi-pass translocon complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs75620555 | 19:3,184,010 | C/G | regulatory region variant | — |
| rs147675154 | 19:3,186,110 | G/A | — | uncertain significance |
| rs200946193 | 19:3,186,137 | C/G | — | uncertain significance |
| rs1291809887 | 19:3,186,177 | G/T | — | uncertain significance |
| rs370383654 | 19:3,192,474 | G/A | — | uncertain significance |
| rs553503742 | 19:3,192,546 | G/A | — | uncertain significance |
| rs764081362 | 19:3,192,624 | G/A | — | uncertain significance |
| rs778733140 | 19:3,192,635 | G/A | — | uncertain significance |
| rs1167099141 | 19:3,192,645 | A/G | — | uncertain significance |
| rs200277850 | 19:3,192,650 | G/A | — | uncertain significance |
| rs200789264 | 19:3,192,657 | G/A | — | likely benign |
| rs373043932 | 19:3,193,376 | A/G | — | uncertain significance |
| rs1057519322 | 19:3,193,402 | C/T | stop gained | pathogenic |
| rs758662558 | 19:3,193,411 | G/A | — | uncertain significance |
| rs745739355 | 19:3,196,205 | A/G | — | uncertain significance |
| rs771930189 | 19:3,196,207 | G/A | — | uncertain significance |
| rs779305762 | 19:3,196,259 | T/G | — | uncertain significance |
| rs187629347 | 19:3,196,284 | C/T | — | benign |
| rs746900941 | 19:3,198,825 | C/T | — | uncertain significance |
| rs2512077411 | 19:3,198,834 | G/A | — | uncertain significance |
| rs1916126285 | 19:3,201,536 | G/A | — | uncertain significance |
| rs1205817573 | 19:3,201,612 | G/T | — | uncertain significance |
| rs182139911 | 19:3,201,634 | G/A | intron variant | — |
| rs144284241 | 19:3,203,962 | C/T | regulatory region variant | — |
| rs1339281470 | 19:3,204,083 | G/C | — | uncertain significance |
| rs745689989 | 19:3,204,129 | G/A | — | uncertain significance |
| rs1478129358 | 19:3,204,611 | T/G | — | uncertain significance |
| rs1201149553 | 19:3,204,619 | C/T | — | uncertain significance |
| rs149150446 | 19:3,204,721 | G/A | — | uncertain significance |
| rs2512083713 | 19:3,204,725 | A/C | — | uncertain significance |
| rs538467615 | 19:3,206,012 | C/A | — | uncertain significance |
| rs368969267 | 19:3,206,278 | C/A | — | uncertain significance |
| rs759323368 | 19:3,206,285 | C/T | — | uncertain significance |
| rs1269485173 | 19:3,206,357 | C/T | — | uncertain significance |
| rs538321269 | 19:3,206,378 | G/A | — | uncertain significance |
| rs748169183 | 19:3,207,218 | G/A | — | uncertain significance |
| rs2512086800 | 19:3,207,390 | G/A | — | uncertain significance |
| rs1916298448 | 19:3,207,397 | C/T | — | uncertain significance |
| rs76473246 | 19:3,207,398 | G/A | — | benign |
| rs1182255722 | 19:3,207,444 | G/A | — | uncertain significance |
| rs375588140 | 19:3,207,456 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.