| Primary Identifier | MGI:1856499 | Allele Type | Spontaneous |
| Gene | Egfr | Inheritance Mode | Recessive |
| Strain of Origin | B10.D2-H2<d>/nSnJ | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | A complementation test with Egfrwa2 identified this mutation as a mutation in Egfr. The molecular lesion in this allele has not been identified. |
