| Primary Identifier | MGI:3033229 | 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 | A to G transition in exon 7 results in a missense mutation and substitution of alanine for threonine at amino acid 228. This same mutation is found in human MODY2 patients. |
