QSOX2
quiescin sulfhydryl oxidase 2
Summary
QSOX2 is a member of the sulfhydryl oxidase/quiescin-6 (Q6) family (QSOX1; MIM 603120) that regulates the sensitization of neuroblastoma cells for IFN-gamma (IFNG; MIM 147570)-induced cell death (Wittke et al., 2003 [PubMed 14633699]).[supplied by OMIM, Jun 2009]
Known Variants60 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1448526603 | 9:139,100,602 | T/A | — | uncertain significance |
| rs1392380852 | 9:139,100,625 | G/C | — | uncertain significance |
| rs1564288123 | 9:139,100,629 | A/G | — | uncertain significance |
| rs370105290 | 9:139,100,666 | C/T | — | uncertain significance |
| rs2490939127 | 9:139,100,725 | G/T | — | uncertain significance |
| rs142355207 | 9:139,100,726 | C/T | — | uncertain significance |
| rs151235947 | 9:139,100,733 | G/A | — | benign |
| rs746508624 | 9:139,100,769 | C/G | — | uncertain significance |
| rs941635962 | 9:139,100,794 | T/A | — | uncertain significance |
| rs763036431 | 9:139,100,807 | G/T | — | uncertain significance |
| rs998662880 | 9:139,100,851 | T/A | — | uncertain significance |
| rs757951204 | 9:139,100,860 | C/T | — | likely benign |
| rs201225826 | 9:139,100,882 | G/T | — | uncertain significance |
| rs1426526630 | 9:139,100,890 | A/G | — | uncertain significance |
| rs761945323 | 9:139,100,911 | C/T | — | uncertain significance |
| rs201357152 | 9:139,100,966 | C/G | — | uncertain significance |
| rs374591343 | 9:139,100,978 | C/T | — | uncertain significance |
| rs148017914 | 9:139,103,119 | G/A | — | uncertain significance |
| rs145948763 | 9:139,103,220 | C/G | — | uncertain significance |
| rs373864386 | 9:139,103,251 | C/T | — | likely benign |
| rs2490944082 | 9:139,103,257 | T/A | — | uncertain significance |
| rs144728279 | 9:139,107,029 | G/A | — | uncertain significance |
| rs1356902410 | 9:139,107,119 | T/C | — | uncertain significance |
| rs375455213 | 9:139,107,131 | G/T | — | uncertain significance |
| rs2490949707 | 9:139,107,135 | G/C | — | uncertain significance |
| rs200166292 | 9:139,108,475 | C/T | — | uncertain significance |
| rs72773790 | 9:139,109,080 | T/C | intron variant | — |
| rs1831943515 | 9:139,110,544 | A/G | — | uncertain significance |
| rs747175246 | 9:139,110,640 | G/A | — | uncertain significance |
| rs2490955422 | 9:139,110,913 | C/T | — | uncertain significance |
| rs142403115 | 9:139,110,935 | C/T | — | likely benign |
| rs1385954800 | 9:139,110,994 | C/T | — | uncertain significance |
| rs7849585 | 9:139,111,870 | G/T | intron variant | — |
| rs201972372 | 9:139,113,660 | G/A | — | uncertain significance |
| rs750834525 | 9:139,115,613 | C/A | — | uncertain significance |
| rs769585779 | 9:139,115,614 | G/A | — | uncertain significance |
| rs2490961950 | 9:139,115,667 | C/T | — | likely benign |
| rs769744648 | 9:139,115,668 | G/A | — | uncertain significance |
| rs148593601 | 9:139,115,869 | G/A | — | uncertain significance |
| rs199562922 | 9:139,115,887 | G/A | — | uncertain significance |
| rs967541020 | 9:139,116,727 | G/T | — | uncertain significance |
| rs1830286437 | 9:139,118,622 | G/A | — | uncertain significance |
| rs928242771 | 9:139,118,654 | T/C | — | likely benign |
| rs747314448 | 9:139,118,700 | C/T | — | uncertain significance |
| rs144677667 | 9:139,118,702 | C/T | — | uncertain significance |
| rs745954157 | 9:139,118,704 | A/C | — | uncertain significance |
| rs12338076 | 9:139,121,740 | A/T | — | — |
| rs4842133 | 9:139,127,566 | C/A | intron variant | — |
| rs11103398 | 9:139,134,474 | T/C | intron variant | — |
| rs782394109 | 9:139,137,336 | G/C | — | uncertain significance |
| rs2490989376 | 9:139,137,385 | A/T | — | uncertain significance |
| rs2490989408 | 9:139,137,399 | A/C | — | uncertain significance |
| rs1268553798 | 9:139,137,433 | C/A | — | uncertain significance |
| rs570092339 | 9:139,137,445 | C/G | — | uncertain significance |
| rs2490989598 | 9:139,137,462 | A/G | — | uncertain significance |
| rs1222759250 | 9:139,137,507 | C/T | — | uncertain significance |
| rs1830469459 | 9:139,137,585 | G/A | — | uncertain significance |
| rs1554758468 | 9:139,137,595 | C/T | — | uncertain significance |
| rs549282673 | 9:139,137,625 | C/T | — | uncertain significance |
| rs1228778827 | 9:139,137,637 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.