| Primary Identifier | MGI:7638770 | Allele Type | Spontaneous |
| Attribute String | Not Specified | Gene | rd22 |
| Inheritance Mode | Recessive | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | This spontaneous mutation mapped to an interval between D12Mit158 and D12Mit133 and has not been proven to be caused by a mutation in Ttll5, but retinal cDNA sequence for Ttll5 shows a G to A point substitution in the 5th base of the 3-prime UTR and a duplication of 122 base pairs beginning at the 7th base pair of the 3-prime UTR. |
