PLCL2
phospholipase C like 2
Summary
Enables GABA receptor binding 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 act upstream of or within B cell proliferation involved in immune response; B-1a B cell differentiation; and negative regulation of B cell receptor signaling pathway. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs114766804 | 3:16,928,027 | T/C | intron variant | — |
| rs1992382 | 3:16,928,092 | G/A | intron variant | — |
| rs1992383 | 3:16,928,137 | G/C | intron variant | — |
| rs116480867 | 3:16,928,621 | C/T | intron variant | — |
| rs6777965 | 3:16,929,593 | C/G | — | — |
| rs79843017 | 3:16,932,366 | A/G | intron variant | — |
| rs10510468 | 3:16,938,623 | G/T | intron variant | — |
| rs142289859 | 3:16,954,941 | T/C | intron variant | — |
| rs1372072 | 3:16,955,259 | G/C | — | — |
| rs74509702 | 3:16,959,964 | G/A | intron variant | — |
| rs6783769 | 3:16,966,423 | G/A | — | — |
| rs9821630 | 3:16,970,938 | A/T | — | — |
| rs4685408 | 3:16,996,035 | G/A | intron variant | — |
| rs3906814 | 3:17,011,474 | C/G | intron variant | — |
| rs73039077 | 3:17,036,387 | G/C | intron variant | — |
| rs7617779 | 3:17,045,586 | A/C | — | — |
| rs5019428 | 3:17,046,866 | G/C | — | — |
| rs4452313 | 3:17,047,032 | A/C | — | — |
| rs2546733657 | 3:17,051,903 | A/G | — | likely benign |
| rs776884102 | 3:17,052,200 | C/T | — | benign |
| rs4602367 | 3:17,053,499 | A/G | synonymous variant | — |
| rs74332311 | 3:17,056,278 | C/T | — | benign |
| rs6776032 | 3:17,064,893 | C/T | — | — |
| rs4535211 | 3:17,072,997 | A/G | intron variant | — |
| rs4685422 | 3:17,110,874 | G/A | intron variant | — |
| rs4685423 | 3:17,114,920 | C/G | — | — |
| rs111333873 | 3:17,123,818 | T/G | intron variant | — |
| rs4618210 | 3:17,124,384 | A/G | intron variant | — |
| rs60111091 | 3:17,131,402 | T/G | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.