CLUL1
clusterin like 1
Summary
Predicted to enable misfolded protein binding activity. Predicted to be located in extracellular region. Predicted to be active in extracellular space and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs191381354 | 18:602,883 | T/C | downstream gene variant | — |
| rs766168896 | 18:618,032 | G/T | — | uncertain significance |
| rs758691813 | 18:618,061 | G/A | — | uncertain significance |
| rs200703485 | 18:618,067 | A/G | — | uncertain significance |
| rs2509940973 | 18:619,260 | G/C | — | uncertain significance |
| rs1043732643 | 18:619,282 | T/C | — | uncertain significance |
| rs895852297 | 18:619,313 | A/T | — | uncertain significance |
| rs371171982 | 18:624,878 | T/A | — | uncertain significance |
| rs760704789 | 18:624,955 | T/C | — | uncertain significance |
| rs370390666 | 18:624,968 | T/C | — | uncertain significance |
| rs368036645 | 18:625,004 | A/C | — | uncertain significance |
| rs890279081 | 18:625,012 | T/C | — | uncertain significance |
| rs1161551213 | 18:627,200 | A/G | — | uncertain significance |
| rs766077524 | 18:627,250 | T/A | — | uncertain significance |
| rs753466551 | 18:627,251 | C/G | — | uncertain significance |
| rs200242838 | 18:627,274 | G/A | — | uncertain significance |
| rs550555452 | 18:627,313 | C/G | — | uncertain significance |
| rs529629931 | 18:627,325 | A/G | — | uncertain significance |
| rs2509964307 | 18:627,328 | T/C | — | uncertain significance |
| rs533292951 | 18:633,027 | C/G | — | — |
| rs2509980559 | 18:633,326 | G/T | — | uncertain significance |
| rs2509980565 | 18:633,327 | A/T | — | uncertain significance |
| rs368695647 | 18:633,345 | A/G | — | uncertain significance |
| rs2509980782 | 18:633,366 | G/T | — | uncertain significance |
| rs779281882 | 18:633,370 | A/G | — | uncertain significance |
| rs2510000754 | 18:641,341 | C/A | — | uncertain significance |
| rs527661052 | 18:641,365 | G/A | — | uncertain significance |
| rs761168896 | 18:641,536 | A/G | — | uncertain significance |
| rs2074431690 | 18:644,962 | T/C | — | uncertain significance |
| rs1188686355 | 18:645,034 | C/T | — | uncertain significance |
| rs12458057 | 18:645,655 | G/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.