| Primary Identifier | MGI:1856307 | Allele Type | Chemically and radiation induced |
| Gene | Tyr | Inheritance Mode | Recessive |
| Strain of Origin | (C3H/HeH x 101/H)F1 | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | The defect is a G-to-T point mutation, altering serine to isoleucine at position 146 or 128 (p.S146I in pre-protein, p.S128I in mature protein) in the encoded protein. |
