PAOX
polyamine oxidase
Summary
Enables polyamine oxidase activity. Involved in polyamine metabolic process and positive regulation of spermidine biosynthetic process. Predicted to be located in cytosol and peroxisomal matrix. Predicted to be active in cytoplasm. Implicated in lung non-small cell carcinoma. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1849284047 | 10:135,192,894 | G/T | — | uncertain significance |
| rs995390471 | 10:135,192,920 | G/T | — | uncertain significance |
| rs1295602208 | 10:135,192,948 | T/C | — | uncertain significance |
| rs944947936 | 10:135,192,983 | C/T | — | uncertain significance |
| rs770874285 | 10:135,192,984 | G/A | — | uncertain significance |
| rs374608714 | 10:135,193,508 | G/A | — | uncertain significance |
| rs781058801 | 10:135,193,548 | G/T | — | uncertain significance |
| rs563058344 | 10:135,193,603 | G/A | — | likely benign |
| rs1019643710 | 10:135,193,667 | G/T | — | uncertain significance |
| rs753690252 | 10:135,193,704 | C/T | — | uncertain significance |
| rs1849322345 | 10:135,193,713 | C/G | — | uncertain significance |
| rs775971773 | 10:135,193,727 | G/A | — | uncertain significance |
| rs900884214 | 10:135,194,965 | G/A | — | uncertain significance |
| rs139393085 | 10:135,195,101 | C/T | — | likely benign |
| rs1007265875 | 10:135,195,107 | A/G | — | uncertain significance |
| rs759077399 | 10:135,195,158 | C/T | — | uncertain significance |
| rs77004335 | 10:135,195,356 | C/T | upstream gene variant | — |
| rs4838735 | 10:135,196,301 | C/A | upstream gene variant | — |
| rs11101729 | 10:135,197,051 | G/A | upstream gene variant | — |
| rs11101730 | 10:135,197,336 | A/T | upstream gene variant | — |
| rs144695264 | 10:135,197,469 | C/A | — | uncertain significance |
| rs367664206 | 10:135,197,582 | G/T | — | uncertain significance |
| rs777691415 | 10:135,197,603 | C/G | — | uncertain significance |
| rs376605515 | 10:135,197,605 | A/G | — | uncertain significance |
| rs2493882422 | 10:135,197,666 | G/C | — | uncertain significance |
| rs540263187 | 10:135,197,689 | T/C | — | uncertain significance |
| rs149870806 | 10:135,202,480 | G/A | — | uncertain significance |
| rs572623831 | 10:135,202,490 | C/T | — | likely benign |
| rs905595124 | 10:135,202,510 | T/C | — | uncertain significance |
| rs112369139 | 10:135,202,538 | T/C | — | likely benign |
| rs767920735 | 10:135,202,560 | C/T | — | uncertain significance |
| rs531281583 | 10:135,203,129 | C/T | — | uncertain significance |
| rs147810590 | 10:135,203,135 | C/T | — | likely benign |
| rs2493901007 | 10:135,203,169 | A/C | — | uncertain significance |
| rs1178874946 | 10:135,203,219 | C/G | — | uncertain significance |
| rs375587914 | 10:135,203,240 | G/A | — | likely benign |
| rs376638594 | 10:135,203,243 | G/A | — | uncertain significance |
| rs2493908204 | 10:135,204,817 | T/A | — | uncertain significance |
| rs149574308 | 10:135,204,854 | G/A | — | likely benign |
| rs367874686 | 10:135,204,868 | C/T | — | uncertain significance |
| rs146088141 | 10:135,204,872 | C/T | — | likely benign |
| rs200635963 | 10:135,204,906 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.