| Primary Identifier | MGI:5004953 | Allele Type | Chemically induced (ENU) |
| Gene | Ptch1 | Strain of Origin | 129S1/Sv or C57BL/6 |
| Is Recombinase | false | Is Wild Type | false |
| molecularNote | This phenotypic mutant was generated in an ENU mutagenesis screen for early craniofacial development phenotypes. Genome sequencing revealed a T to A nucleotide change in intron 15, which created a new splice acceptor site, resulting in a premature stop codon in exon 16 and generation of a truncated protein. |
