Primary Identifier | MGI:3621484 | Allele Type | Spontaneous |
Gene | Spta1 | Inheritance Mode | Recessive |
Strain of Origin | NOD/ShiLtJ | Is Recombinase | false |
Is Wild Type | false |
molecularNote | The mutation is a C-to-T transition in exon 43 that results in substitution of histidine with tyrosine at amino acid position 2012 (p.H2012Y). |