| Primary Identifier | MGI:4999725 | Allele Type | Spontaneous |
| Gene | Oca2 | Inheritance Mode | Recessive |
| Strain of Origin | B10.RIII-H2<r> H2-T18<b>/(71NS)SnJ | Is Recombinase | false |
| Is Wild Type | false |
| description | This allele has been discontinued as a mouse strain at The Jackson Laboratory but is available as DNA, JR 014100, B10.Cg-H2r H2-T18b Oca2p-18J/GrsrJ |
| molecularNote | This spontaneous mutation was proven allelic with Oca2p by a failed complementation tests. A single C-to-A nucleotide transversion was identified at position 56,357,112 (GRCm38), changing alanine codon 649 to aspartic acid (p.A649D). |
