Primary Identifier | MGI:5578570 | Allele Type | Chemically induced (ENU) |
Attribute String | Not Specified | Gene | Ampd3 |
Inheritance Mode | Dominant | Strain of Origin | SJL/J |
Is Recombinase | false | Is Wild Type | false |
molecularNote | The molecular lesion is an A-to-G base substitution at location 7:117953361. This results in a substitution of alanine for threonine at position 689 in the encoded protein. |