PLPPR3
phospholipid phosphatase related 3
Summary
The proteins in the lipid phosphate phosphatase (LPP) family, including PRG2, are integral membrane proteins that modulate bioactive lipid phosphates including phosphatidate, lysophosphatidate, and sphingosine-1-phosphate in the context of cell migration, neurite retraction, and mitogenesis (Brauer et al., 2003 [PubMed 12730698]).[supplied by OMIM, Mar 2008]
Known Variants79 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2034943375 | 19:812,589 | G/A | — | uncertain significance |
| rs891729946 | 19:812,595 | A/T | — | uncertain significance |
| rs1484469865 | 19:812,649 | A/G | — | uncertain significance |
| rs932961110 | 19:812,682 | C/G | — | uncertain significance |
| rs1398759106 | 19:812,691 | G/A | — | uncertain significance |
| rs1306544765 | 19:812,700 | G/T | — | uncertain significance |
| rs1164495464 | 19:812,712 | G/A | — | uncertain significance |
| rs891677636 | 19:812,722 | G/A | — | uncertain significance |
| rs945996181 | 19:812,725 | G/C | — | uncertain significance |
| rs1001609628 | 19:812,739 | G/A | — | uncertain significance |
| rs2512113217 | 19:812,740 | T/C | — | uncertain significance |
| rs1025653044 | 19:812,779 | C/G | — | uncertain significance |
| rs987097379 | 19:812,820 | C/G | — | uncertain significance |
| rs1043390466 | 19:812,823 | G/C | — | uncertain significance |
| rs1311030776 | 19:812,847 | C/T | — | uncertain significance |
| rs1234188631 | 19:812,918 | C/G | — | uncertain significance |
| rs558230542 | 19:812,946 | T/C | — | uncertain significance |
| rs551920844 | 19:812,971 | G/A | — | uncertain significance |
| rs778561610 | 19:812,983 | T/C | — | uncertain significance |
| rs749603336 | 19:813,012 | G/A | — | uncertain significance |
| rs2034963881 | 19:813,027 | G/A | — | uncertain significance |
| rs757959111 | 19:813,054 | G/A | — | uncertain significance |
| rs756890234 | 19:813,130 | G/A | — | uncertain significance |
| rs763941209 | 19:813,211 | C/T | — | uncertain significance |
| rs751823702 | 19:813,235 | C/T | — | uncertain significance |
| rs749231494 | 19:813,255 | G/A | — | uncertain significance |
| rs527549059 | 19:813,285 | C/A | — | uncertain significance |
| rs2034975377 | 19:813,301 | G/T | — | uncertain significance |
| rs765899709 | 19:813,324 | A/C | — | uncertain significance |
| rs958380808 | 19:813,333 | G/C | — | uncertain significance |
| rs991169314 | 19:813,336 | G/A | — | uncertain significance |
| rs750649743 | 19:813,382 | C/T | — | uncertain significance |
| rs780159532 | 19:813,386 | C/G | — | uncertain significance |
| rs746674994 | 19:813,501 | C/T | — | uncertain significance |
| rs530245812 | 19:813,547 | T/C | — | uncertain significance |
| rs756868110 | 19:813,595 | G/A | — | uncertain significance |
| rs1397804140 | 19:813,642 | C/T | — | uncertain significance |
| rs1447052647 | 19:813,687 | C/T | — | uncertain significance |
| rs1208247703 | 19:813,701 | C/G | — | likely benign |
| rs1458486162 | 19:813,705 | C/G | — | uncertain significance |
| rs1486948027 | 19:813,706 | G/A | — | uncertain significance |
| rs2034994751 | 19:813,715 | G/A | — | uncertain significance |
| rs1340097743 | 19:813,718 | G/A | — | uncertain significance |
| rs755722115 | 19:813,774 | T/C | — | uncertain significance |
| rs942553845 | 19:813,777 | T/C | — | uncertain significance |
| rs779560227 | 19:813,793 | C/T | — | uncertain significance |
| rs748738596 | 19:813,794 | G/C | — | uncertain significance |
| rs1013829871 | 19:813,832 | C/T | — | uncertain significance |
| rs972162299 | 19:813,861 | G/A | — | uncertain significance |
| rs916855339 | 19:813,862 | G/C | — | uncertain significance |
| rs771294478 | 19:814,453 | G/A | — | uncertain significance |
| rs760529206 | 19:814,487 | G/A | — | uncertain significance |
| rs763679235 | 19:814,540 | G/A | — | uncertain significance |
| rs143355871 | 19:814,547 | C/T | — | uncertain significance |
| rs1194483325 | 19:814,636 | G/A | — | uncertain significance |
| rs147509070 | 19:814,648 | G/A | — | uncertain significance |
| rs745799043 | 19:814,661 | C/T | — | uncertain significance |
| rs143962053 | 19:814,684 | G/A | — | uncertain significance |
| rs377665274 | 19:814,706 | C/T | — | uncertain significance |
| rs200639651 | 19:814,917 | C/T | — | uncertain significance |
| rs753912348 | 19:814,943 | G/A | — | uncertain significance |
| rs777402250 | 19:814,961 | G/A | — | uncertain significance |
| rs2512121373 | 19:815,007 | G/A | — | uncertain significance |
| rs759749607 | 19:815,021 | G/A | — | uncertain significance |
| rs146481415 | 19:815,195 | G/A | — | uncertain significance |
| rs150002055 | 19:815,206 | C/T | — | uncertain significance |
| rs200612058 | 19:815,234 | C/T | — | uncertain significance |
| rs748160295 | 19:815,239 | T/C | — | uncertain significance |
| rs904882797 | 19:815,249 | C/T | — | uncertain significance |
| rs976495091 | 19:815,309 | T/A | — | uncertain significance |
| rs375585666 | 19:815,671 | C/T | — | uncertain significance |
| rs201659263 | 19:815,800 | C/T | — | uncertain significance |
| rs761905550 | 19:815,832 | G/A | — | uncertain significance |
| rs72982156 | 19:816,540 | T/C | — | — |
| rs2512131856 | 19:821,490 | C/G | — | uncertain significance |
| rs779967897 | 19:821,523 | C/G | — | uncertain significance |
| rs910087103 | 19:821,528 | G/C | — | uncertain significance |
| rs954546750 | 19:821,529 | G/C | — | uncertain significance |
| rs150524534 | 19:821,542 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.