CPA4
carboxypeptidase A4
Summary
This gene is a member of the carboxypeptidase A/B subfamily, and it is located in a cluster with three other family members on chromosome 7. Carboxypeptidases are zinc-containing exopeptidases that catalyze the release of carboxy-terminal amino acids, and are synthesized as zymogens that are activated by proteolytic cleavage. This gene could be involved in the histone hyperacetylation pathway. It is imprinted and may be a strong candidate gene for prostate cancer aggressiveness. [provided by RefSeq, Jul 2008]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs771082708 | 7:129,938,611 | A/G | — | uncertain significance |
| rs1011554643 | 7:129,939,144 | G/A | — | uncertain significance |
| rs2535713646 | 7:129,939,155 | G/A | — | uncertain significance |
| rs372031946 | 7:129,939,161 | G/A | — | uncertain significance |
| rs1418112193 | 7:129,939,209 | G/A | — | uncertain significance |
| rs1341282367 | 7:129,939,242 | C/A | — | uncertain significance |
| rs961771358 | 7:129,940,717 | A/G | — | uncertain significance |
| rs555570892 | 7:129,944,198 | T/C | — | — |
| rs578138591 | 7:129,944,327 | G/A | — | uncertain significance |
| rs766625502 | 7:129,944,334 | A/G | — | uncertain significance |
| rs754551102 | 7:129,944,377 | G/T | — | uncertain significance |
| rs367921847 | 7:129,944,399 | C/T | — | uncertain significance |
| rs368665966 | 7:129,945,684 | C/T | — | uncertain significance |
| rs770077714 | 7:129,946,661 | C/T | — | uncertain significance |
| rs771641019 | 7:129,946,674 | G/T | — | uncertain significance |
| rs1793829779 | 7:129,946,715 | G/T | — | uncertain significance |
| rs7787960 | 7:129,947,454 | G/A | intron variant | — |
| rs145012020 | 7:129,948,221 | G/A | — | likely benign |
| rs570075096 | 7:129,950,677 | G/A | — | uncertain significance |
| rs201774085 | 7:129,950,681 | A/G | — | uncertain significance |
| rs763242315 | 7:129,950,684 | C/T | — | uncertain significance |
| rs768232162 | 7:129,950,690 | T/C | — | uncertain significance |
| rs2171492 | 7:129,950,740 | G/T | missense variant | — |
| rs1765262289 | 7:129,950,757 | C/G | — | uncertain significance |
| rs147134098 | 7:129,950,765 | C/T | — | uncertain significance |
| rs375886402 | 7:129,950,789 | G/A | — | uncertain significance |
| rs143094036 | 7:129,962,366 | C/A | — | uncertain significance |
| rs771428963 | 7:129,962,370 | G/A | — | uncertain significance |
| rs138648309 | 7:129,962,488 | T/C | — | uncertain significance |
| rs748012321 | 7:129,962,490 | G/A | — | uncertain significance |
| rs763081297 | 7:129,962,499 | C/T | — | uncertain significance |
| rs761843253 | 7:129,962,507 | C/A | — | uncertain significance |
| rs376985428 | 7:129,962,512 | A/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.