| Primary Identifier | MGI:3034162 | Allele Type | Chemically induced (ENU) |
| Gene | Nox3 | Inheritance Mode | Recessive |
| Strain of Origin | C3H | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | The mutation in the R542 mouse was identified as an A-to-G substitution at coding nucleotide position 1516 (c.1516A>G), replacing a lysine residue with a glutamic acid at postion 506 (p.K506E). The lysine residue is part of the putative NADPH binding site. |
