| Primary Identifier | MGI:2671784 | Allele Type | Chemically induced (ENU) |
| Gene | Zfp423 | Inheritance Mode | Recessive |
| Strain of Origin | C57BL/6J | Is Recombinase | false |
| Is Wild Type | false | Project Collection | Mutagenesis for Dev. Defects |
| description | Phenotypic Similarity to Human Syndrome: Cerebellar vermis hypoplasia (J:114758). |
| molecularNote | This phenotypic mutant was identified in an ENU mutagenesis screen at the Baylor College of Medicine. A C-to-T transition mutation in the fourth exon results in the introduction of a premature stop codon. Western blot analysis showed that no detectable protein was expressed from this allele. |
