MOXD1
monooxygenase DBH like 1
Summary
Predicted to enable copper ion binding activity and dopamine beta-monooxygenase activity. Predicted to be involved in dopamine catabolic process; norepinephrine biosynthetic process; and octopamine biosynthetic process. Part of endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6902875 | 6:132,617,072 | A/G | downstream gene variant | — |
| rs142389314 | 6:132,618,314 | G/A | — | uncertain significance |
| rs2482459943 | 6:132,618,441 | C/A | — | uncertain significance |
| rs748046713 | 6:132,618,927 | G/A | — | uncertain significance |
| rs776614952 | 6:132,619,051 | G/A | — | uncertain significance |
| rs4897574 | 6:132,623,184 | C/A | — | — |
| rs770639429 | 6:132,636,781 | G/T | — | uncertain significance |
| rs762337716 | 6:132,636,805 | T/A | — | uncertain significance |
| rs199952832 | 6:132,636,849 | G/A | — | uncertain significance |
| rs1286558079 | 6:132,636,861 | C/A | — | uncertain significance |
| rs966635220 | 6:132,636,877 | G/T | — | uncertain significance |
| rs531459123 | 6:132,636,885 | A/T | — | uncertain significance |
| rs201228813 | 6:132,636,906 | C/T | — | uncertain significance |
| rs375489900 | 6:132,641,796 | T/C | — | uncertain significance |
| rs138817081 | 6:132,641,803 | G/A | — | uncertain significance |
| rs589756 | 6:132,643,117 | C/T | — | — |
| rs767282374 | 6:132,643,864 | T/C | — | uncertain significance |
| rs983736507 | 6:132,643,873 | A/G | — | uncertain significance |
| rs1775103173 | 6:132,643,892 | G/A | — | uncertain significance |
| rs201058024 | 6:132,643,915 | C/T | — | uncertain significance |
| rs752440623 | 6:132,643,925 | G/T | — | uncertain significance |
| rs142837226 | 6:132,643,977 | A/T | — | uncertain significance |
| rs200855350 | 6:132,645,077 | A/G | — | uncertain significance |
| rs2482547132 | 6:132,645,090 | T/A | — | uncertain significance |
| rs2482547323 | 6:132,645,119 | A/G | — | uncertain significance |
| rs779261453 | 6:132,645,126 | G/A | — | uncertain significance |
| rs1291415188 | 6:132,645,174 | C/G | — | uncertain significance |
| rs148803041 | 6:132,649,565 | T/C | — | uncertain significance |
| rs147693794 | 6:132,649,650 | G/T | — | uncertain significance |
| rs1773410152 | 6:132,649,694 | G/A | — | uncertain significance |
| rs188993886 | 6:132,659,142 | A/T | intron variant | — |
| rs118178463 | 6:132,662,999 | G/A | regulatory region variant | — |
| rs777762067 | 6:132,693,760 | T/C | — | uncertain significance |
| rs1465719276 | 6:132,693,817 | T/C | — | uncertain significance |
| rs1312044346 | 6:132,695,801 | T/C | — | uncertain significance |
| rs769723338 | 6:132,695,805 | G/T | — | uncertain significance |
| rs146200701 | 6:132,695,900 | G/A | — | uncertain significance |
| rs185973243 | 6:132,697,673 | G/A | intron variant | — |
| rs201008601 | 6:132,722,429 | C/T | — | uncertain significance |
| rs755926570 | 6:132,722,433 | C/G | — | uncertain significance |
| rs2482780421 | 6:132,722,466 | C/T | — | uncertain significance |
| rs771758982 | 6:132,722,480 | G/T | — | uncertain significance |
| rs1465524802 | 6:132,722,507 | C/T | — | uncertain significance |
| rs766791952 | 6:132,722,511 | C/A | — | uncertain significance |
| rs1483784510 | 6:132,722,529 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.