LPCAT3
lysophosphatidylcholine acyltransferase 3
Summary
Enables 1-acylglycerophosphocholine O-acyltransferase activity; 1-acylglycerophosphoethanolamine O-acyltransferase activity; and 1-acylglycerophosphoserine O-acyltransferase activity. Involved in phosphatidylcholine acyl-chain remodeling; phosphatidylethanolamine acyl-chain remodeling; and phosphatidylserine acyl-chain remodeling. Located in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs199705379 | 12:7,085,009 | T/C | downstream gene variant | — |
| rs1405137368 | 12:7,086,317 | C/G | — | uncertain significance |
| rs782718258 | 12:7,086,370 | T/C | — | uncertain significance |
| rs781810040 | 12:7,086,391 | A/T | — | uncertain significance |
| rs921327898 | 12:7,086,393 | A/G | — | uncertain significance |
| rs1035421832 | 12:7,086,659 | G/A | — | uncertain significance |
| rs782278519 | 12:7,086,887 | T/C | — | uncertain significance |
| rs372779694 | 12:7,087,510 | C/G | — | uncertain significance |
| rs1555153591 | 12:7,087,519 | T/G | — | uncertain significance |
| rs1565596659 | 12:7,087,542 | A/G | — | uncertain significance |
| rs200922476 | 12:7,087,551 | G/A | — | uncertain significance |
| rs1555153647 | 12:7,087,821 | T/C | — | uncertain significance |
| rs61170325 | 12:7,089,613 | A/C | — | — |
| rs782324010 | 12:7,090,307 | C/G | — | uncertain significance |
| rs60718946 | 12:7,091,021 | G/A | — | benign |
| rs200178788 | 12:7,091,071 | A/G | — | benign |
| rs367654948 | 12:7,091,857 | T/C | — | uncertain significance |
| rs142589366 | 12:7,091,863 | C/T | — | uncertain significance |
| rs782492797 | 12:7,091,877 | C/T | — | uncertain significance |
| rs139480947 | 12:7,091,883 | A/G | — | uncertain significance |
| rs376479324 | 12:7,091,893 | G/C | — | uncertain significance |
| rs781806022 | 12:7,092,638 | G/A | — | uncertain significance |
| rs148310884 | 12:7,096,102 | T/C | upstream gene variant | — |
| rs748097723 | 12:7,102,857 | C/T | — | — |
| rs3867477 | 12:7,111,062 | T/A | — | — |
| rs57301478 | 12:7,111,184 | A/C | — | — |
| rs60015123 | 12:7,112,902 | T/C | intron variant | — |
| rs58845597 | 12:7,120,942 | T/C | intron variant | — |
| rs192308173 | 12:7,121,127 | G/A | intron variant | — |
| rs2539564614 | 12:7,125,655 | T/C | — | uncertain significance |
| rs782445575 | 12:7,125,677 | C/A | — | uncertain significance |
| rs782726275 | 12:7,125,685 | A/G | — | uncertain significance |
| rs781813073 | 12:7,125,716 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.