| Primary Identifier | MGI:1857018 | Allele Type | Spontaneous |
| Attribute String | Humanized sequence, Hypomorph | Gene | Oat |
| Inheritance Mode | Recessive | Strain of Origin | AKR/J |
| Is Recombinase | false | Is Wild Type | false |
| molecularNote | A spontaneous G-to-C transversion in exon 9 causes a glycine to alanine substitution at amino acid 353 (p.G353A), an evolutionarily conserved residue. This glycine is mutated in at least one family with gyrate atrophy of the choroid and retina. |
