ACP6
acid phosphatase 6, lysophosphatidic
Summary
This gene encodes a member of the histidine acid phosphatase protein family. The encoded protein hydrolyzes lysophosphatidic acid, which is involved in G protein-coupled receptor signaling, lipid raft modulation, and in balancing lipid composition within the cell. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2016]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs80296758 | 1:147,101,355 | T/C | downstream gene variant | — |
| rs137969432 | 1:147,105,804 | T/C | intron variant | — |
| rs142461278 | 1:147,106,270 | T/C | intron variant | — |
| rs139302755 | 1:147,113,521 | T/C | downstream gene variant | — |
| rs57463094 | 1:147,118,006 | T/C | 3 prime UTR variant | — |
| rs781853603 | 1:147,119,247 | A/G | — | uncertain significance |
| rs782505855 | 1:147,119,306 | C/T | — | uncertain significance |
| rs114396949 | 1:147,119,308 | T/C | — | benign |
| rs146616655 | 1:147,120,053 | C/T | — | uncertain significance |
| rs782629079 | 1:147,120,072 | A/T | — | uncertain significance |
| rs782395582 | 1:147,120,078 | C/A | — | uncertain significance |
| rs79489938 | 1:147,121,000 | G/A | intron variant | — |
| rs782414489 | 1:147,121,956 | C/T | — | likely benign |
| rs140258721 | 1:147,126,320 | C/T | — | uncertain significance |
| rs782552755 | 1:147,126,323 | C/T | — | likely benign |
| rs782246421 | 1:147,126,356 | C/T | — | uncertain significance |
| rs1443058005 | 1:147,126,377 | T/C | — | likely benign |
| rs201893716 | 1:147,126,416 | G/C | — | uncertain significance |
| rs11541487 | 1:147,126,417 | T/C | — | benign |
| rs2526776925 | 1:147,126,429 | C/G | — | uncertain significance |
| rs140566115 | 1:147,126,437 | G/A | — | benign |
| rs2526781268 | 1:147,127,288 | C/T | — | uncertain significance |
| rs2526781561 | 1:147,127,316 | G/A | — | uncertain significance |
| rs2526781694 | 1:147,127,324 | A/C | — | uncertain significance |
| rs146958747 | 1:147,127,338 | T/G | — | uncertain significance |
| rs12145385 | 1:147,129,786 | G/A | intron variant | — |
| rs978886014 | 1:147,131,132 | G/A | — | uncertain significance |
| rs146298808 | 1:147,131,530 | A/T | — | uncertain significance |
| rs781849731 | 1:147,131,581 | C/T | — | uncertain significance |
| rs144959805 | 1:147,131,611 | C/T | missense variant | pathogenic |
| rs1553212315 | 1:147,131,632 | A/T | — | uncertain significance |
| rs1553212321 | 1:147,131,637 | C/T | — | uncertain significance |
| rs140398965 | 1:147,131,784 | T/C | — | uncertain significance |
| rs374575256 | 1:147,131,809 | T/G | — | uncertain significance |
| rs143599880 | 1:147,133,008 | G/C | intron variant | — |
| rs1336514463 | 1:147,141,989 | G/C | — | uncertain significance |
| rs149388165 | 1:147,142,037 | C/T | — | uncertain significance |
| rs200702109 | 1:147,142,059 | C/T | — | uncertain significance |
| rs1462870297 | 1:147,142,149 | T/C | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.