Primary Identifier | MGI:5607604 | Allele Type | Spontaneous |
Attribute String | Not Specified | Gene | Myo5a |
Inheritance Mode | Recessive | Strain of Origin | BALB/cJ |
Is Recombinase | false | Is Wild Type | false |
molecularNote | This spontaneous mutation is a T-to-C transition at chromosome 9:75,140,731 bp (GRCm38), which is predicted to have a high impact on the exon 7 splice donor site by changing it from G-GT to G-GC. |