PLCL1
phospholipase C like 1 (inactive)
Summary
Predicted to enable GABA receptor binding activity and phosphatidylinositol-4,5-bisphosphate phospholipase C activity. Predicted to be involved in several processes, including gamma-aminobutyric acid signaling pathway; negative regulation of cold-induced thermogenesis; and phosphatidylinositol-mediated signaling. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants84 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2469178419 | 2:198,669,830 | G/C | — | uncertain significance |
| rs2469178518 | 2:198,669,867 | A/C | — | uncertain significance |
| rs1267664086 | 2:198,669,872 | G/A | — | uncertain significance |
| rs1690442294 | 2:198,669,891 | C/T | — | uncertain significance |
| rs1005028494 | 2:198,669,894 | G/A | — | uncertain significance |
| rs1690443549 | 2:198,669,924 | T/A | — | uncertain significance |
| rs958726865 | 2:198,669,930 | C/T | — | uncertain significance |
| rs949343585 | 2:198,669,999 | C/T | — | uncertain significance |
| rs700675 | 2:198,700,216 | G/A | intron variant | — |
| rs16825188 | 2:198,741,134 | G/T | — | — |
| rs6735214 | 2:198,760,507 | C/T | intron variant | — |
| rs62277889 | 2:198,783,693 | C/A | — | — |
| rs376702757 | 2:198,787,412 | T/G | — | — |
| rs61435657 | 2:198,825,506 | G/C | intron variant | — |
| rs1850634 | 2:198,827,896 | T/C | intron variant | — |
| rs10204166 | 2:198,835,264 | C/A | — | — |
| rs1518359 | 2:198,847,383 | C/T | regulatory region variant | — |
| rs1016883 | 2:198,881,668 | G/C | — | — |
| rs12693829 | 2:198,885,425 | G/T | intron variant | — |
| rs2139049 | 2:198,887,660 | G/T | — | — |
| rs6738825 | 2:198,896,895 | A/G | intron variant | — |
| rs17520121 | 2:198,898,718 | T/G | intron variant | — |
| rs892512 | 2:198,905,910 | C/A | intron variant | — |
| rs67031482 | 2:198,911,166 | C/A | — | — |
| rs67748055 | 2:198,911,426 | G/C | — | — |
| rs10497813 | 2:198,914,072 | G/T | intron variant | — |
| rs34388051 | 2:198,929,083 | G/A | intron variant | — |
| rs35657897 | 2:198,929,086 | A/G | intron variant | — |
| rs7572733 | 2:198,929,806 | C/T | intron variant | — |
| rs74688411 | 2:198,934,873 | A/G | intron variant | — |
| rs2164068 | 2:198,943,852 | T/A | intron variant | — |
| rs6716898 | 2:198,944,271 | G/A | intron variant | — |
| rs1022642979 | 2:198,948,643 | T/A | — | uncertain significance |
| rs1692787330 | 2:198,948,743 | C/G | — | uncertain significance |
| rs1692792468 | 2:198,948,868 | T/A | — | uncertain significance |
| rs1005120936 | 2:198,948,962 | T/C | — | uncertain significance |
| rs371442939 | 2:198,948,974 | A/G | — | uncertain significance |
| rs1692797544 | 2:198,949,016 | A/T | — | uncertain significance |
| rs2468857069 | 2:198,949,046 | A/G | — | uncertain significance |
| rs146525330 | 2:198,949,061 | A/G | — | uncertain significance |
| rs61752178 | 2:198,949,074 | C/T | — | likely benign |
| rs140990771 | 2:198,949,131 | G/A | — | uncertain significance |
| rs1244383035 | 2:198,949,250 | C/A | — | uncertain significance |
| rs373797233 | 2:198,949,278 | C/T | — | uncertain significance |
| rs780048494 | 2:198,949,341 | G/A | — | uncertain significance |
| rs766846507 | 2:198,949,377 | A/G | — | uncertain significance |
| rs754994541 | 2:198,949,644 | T/A | — | uncertain significance |
| rs765105645 | 2:198,949,646 | C/G | — | uncertain significance |
| rs780710675 | 2:198,949,685 | G/T | — | uncertain significance |
| rs143432997 | 2:198,949,875 | C/T | — | uncertain significance |
| rs751476038 | 2:198,949,933 | G/A | — | uncertain significance |
| rs148333022 | 2:198,949,949 | G/A | — | uncertain significance |
| rs147098937 | 2:198,949,976 | A/G | — | uncertain significance |
| rs769404805 | 2:198,950,000 | G/A | — | uncertain significance |
| rs146000716 | 2:198,950,035 | G/C | — | uncertain significance |
| rs201079513 | 2:198,950,128 | G/C | — | uncertain significance |
| rs772026588 | 2:198,950,184 | G/A | — | uncertain significance |
| rs1295975332 | 2:198,950,186 | A/T | — | uncertain significance |
| rs545770182 | 2:198,950,227 | T/C | — | likely benign |
| rs1419008718 | 2:198,950,271 | T/G | — | uncertain significance |
| rs144487956 | 2:198,950,287 | G/T | — | benign |
| rs2468860792 | 2:198,950,420 | A/G | — | uncertain significance |
| rs762447591 | 2:198,950,451 | A/G | — | uncertain significance |
| rs1485844471 | 2:198,950,505 | A/G | — | uncertain significance |
| rs1216853108 | 2:198,950,774 | A/T | — | uncertain significance |
| rs199848125 | 2:198,950,859 | C/G | — | uncertain significance |
| rs2468862236 | 2:198,950,891 | G/T | — | uncertain significance |
| rs2468862372 | 2:198,950,930 | G/A | — | uncertain significance |
| rs770796285 | 2:198,950,934 | T/C | — | uncertain significance |
| rs143802664 | 2:198,950,949 | A/G | — | uncertain significance |
| rs142389942 | 2:198,953,588 | A/T | — | conflicting classifications of pathogenicity |
| rs2468865783 | 2:198,953,691 | C/T | — | uncertain significance |
| rs1205673795 | 2:198,953,706 | T/A | — | uncertain significance |
| rs370504499 | 2:198,953,707 | G/T | — | uncertain significance |
| rs41270239 | 2:198,953,793 | A/G | — | likely benign |
| rs7595412 | 2:198,962,243 | G/A | intron variant | — |
| rs3771362 | 2:198,962,831 | C/T | intron variant | — |
| rs139123427 | 2:198,966,025 | G/A | — | uncertain significance |
| rs2228136 | 2:198,966,044 | G/A | — | benign |
| rs202019878 | 2:198,968,575 | A/C | — | uncertain significance |
| rs892515 | 2:198,977,821 | C/A | — | — |
| rs988583 | 2:198,987,935 | C/A | intron variant | — |
| rs2468933314 | 2:199,011,526 | A/G | — | uncertain significance |
| rs1694532279 | 2:199,011,606 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.