NOX5
NADPH oxidase 5
Summary
Enables proton channel activity and superoxide-generating NAD(P)H oxidase activity. Involved in several processes, including endothelial cell proliferation; proton transmembrane transport; and superoxide anion generation. Located in endoplasmic reticulum and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs534536836 | 15:69,256,919 | C/T | — | — |
| rs575250197 | 15:69,318,881 | G/A | — | uncertain significance |
| rs2505207806 | 15:69,318,897 | G/C | — | uncertain significance |
| rs1023485734 | 15:69,318,903 | G/A | — | likely benign |
| rs147937844 | 15:69,318,947 | G/A | — | likely benign |
| rs761647093 | 15:69,318,956 | C/G | — | uncertain significance |
| rs548945801 | 15:69,320,594 | G/A | — | uncertain significance |
| rs147117800 | 15:69,320,601 | G/A | — | uncertain significance |
| rs759200679 | 15:69,320,661 | C/T | — | uncertain significance |
| rs36036826 | 15:69,320,670 | A/T | — | benign |
| rs148321747 | 15:69,320,672 | C/T | — | uncertain significance |
| rs200180547 | 15:69,323,969 | T/C | — | uncertain significance |
| rs751190593 | 15:69,323,974 | A/G | — | uncertain significance |
| rs746394410 | 15:69,324,085 | A/G | — | uncertain significance |
| rs764548905 | 15:69,325,477 | C/A | — | uncertain significance |
| rs143909710 | 15:69,325,529 | C/T | — | uncertain significance |
| rs748888839 | 15:69,325,548 | C/G | — | uncertain significance |
| rs764557559 | 15:69,325,576 | G/C | — | uncertain significance |
| rs2505239221 | 15:69,327,703 | C/T | — | uncertain significance |
| rs575904483 | 15:69,327,709 | C/T | — | uncertain significance |
| rs145609289 | 15:69,327,734 | C/T | — | benign |
| rs34406284 | 15:69,327,737 | G/A | — | benign |
| rs769118589 | 15:69,328,185 | C/T | — | uncertain significance |
| rs1227813483 | 15:69,328,222 | C/A | — | likely benign |
| rs1263191893 | 15:69,328,229 | A/G | — | uncertain significance |
| rs141804052 | 15:69,329,401 | G/A | — | likely benign |
| rs753049513 | 15:69,329,501 | C/T | — | uncertain significance |
| rs764287965 | 15:69,329,503 | C/T | — | uncertain significance |
| rs373906925 | 15:69,329,504 | G/A | — | uncertain significance |
| rs769784392 | 15:69,331,218 | C/T | — | uncertain significance |
| rs145542415 | 15:69,331,221 | C/A | — | uncertain significance |
| rs769615321 | 15:69,331,237 | A/G | — | uncertain significance |
| rs900336435 | 15:69,331,312 | G/A | — | uncertain significance |
| rs1045447166 | 15:69,339,163 | G/T | — | likely benign |
| rs571739852 | 15:69,339,759 | A/G | — | uncertain significance |
| rs759159780 | 15:69,339,813 | G/A | — | uncertain significance |
| rs145431252 | 15:69,339,834 | G/A | — | uncertain significance |
| rs34576567 | 15:69,340,258 | A/G | — | benign |
| rs139553033 | 15:69,341,330 | G/A | — | uncertain significance |
| rs2140278241 | 15:69,341,380 | G/T | — | uncertain significance |
| rs311904 | 15:69,346,946 | T/A | — | — |
| rs769046961 | 15:69,347,676 | C/T | — | uncertain significance |
| rs562414382 | 15:69,347,677 | G/A | — | uncertain significance |
| rs773236709 | 15:69,347,697 | T/C | — | uncertain significance |
| rs774597800 | 15:69,347,806 | C/T | — | uncertain significance |
| rs767570585 | 15:69,347,808 | C/T | — | uncertain significance |
| rs144201182 | 15:69,347,809 | G/A | — | uncertain significance |
| rs527628160 | 15:69,347,824 | G/A | — | uncertain significance |
| rs762503991 | 15:69,348,923 | G/A | — | uncertain significance |
| rs772321172 | 15:69,348,999 | A/G | — | uncertain significance |
| rs7168025 | 15:69,349,013 | A/G | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.