| Primary Identifier | MGI:5484771 | Allele Type | Spontaneous |
| Gene | Ap3d1 | Inheritance Mode | Recessive |
| Strain of Origin | (B6(129P2)-shsn/GrsrJ x BALB/cJ)F2 | Is Recombinase | false |
| Is Wild Type | false |
| description | Because this spontaneous mutation arose on and was characterized on an albino background it is not known whether it causes diluted pigmentation. |
| molecularNote | This spontaneous 8 base pair deletion of GTAGCAGG from chromosome 10 position 80,709,203-210 (GRCm38) causes a frameshift mutation beginning at amino acid position 1098 and subsequent premature termination. |
