| Primary Identifier | MGI:3625823 | Allele Type | Chemically induced (ENU) |
| Gene | Nnt | Strain of Origin | (C3H/HeH x BALB/c)F1 |
| Is Recombinase | false | Is Wild Type | false |
| molecularNote | The mutation was identified as G>A substitution in exon 14, resulting in a nonconservative substitution of glycine by aspartic acid at amino acid 745 (p.G745D; p.G494D in exon 9 in the C57BL/6J strain (which has a 5-exon 251aa deletion)). Western blot analysis demonstrated that expressed protein was present in pancreatic islets of homozygous mice. |
