Primary Identifier | MGI:3033232 | Allele Type | Chemically induced (ENU) |
Gene | Gck | Inheritance Mode | Dominant |
Strain of Origin | C57BL/6J | Is Recombinase | false |
Is Wild Type | false | Project Collection | RIKEN GSC ENU Project |
molecularNote | C to T transition in exon 6 results in a missense mutation and a non conservative substitution for methionine for threonine at amino acid 206. This same mutation is found in human MODY2 patients. |