| Primary Identifier | MGI:2183518 | Allele Type | Radiation induced |
| Gene | Gapdh | Strain of Origin | (101/El x C3H/El)F1 |
| Is Recombinase | false | Is Wild Type | false |
| molecularNote | An X-ray induced mutation that was shown to express 50% of normal levels of the encoded enzyme in heterozygous mice. This mutation as an A to G transition at nucleotide position 926 in exon 5. This causes an isoleucine to serine amino acid residue change at position 308. |
