| Primary Identifier | MGI:1856536 | Allele Type | Spontaneous |
| Gene | Agtpbp1 | Inheritance Mode | Recessive |
| Strain of Origin | SM/J | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | The sequence defect underlying this mutant phenotype was identified a 7.8 kb insertion into intron 13 of the gene. The insertion contains repetitive elements similar to the T cell receptor locus. Northern analysis from cerebellum, heart and brain failed to detect any transcript using a probe from exons 16-19. However, transcript was detected in testis at reduced levels. |
