| Primary Identifier | MGI:7486783 | Allele Type | Chemically induced (ENU) |
| Gene | Chd7 | Inheritance Mode | Dominant |
| Strain of Origin | BALB/c | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | A point mutation in intron 9 (c.3219-18 T > A) created a cryptic splice site. This mutation results in the expression of alternate transcripts including one retaining 16 nt of intron 9 resulting in a frameshift and premature stop codon in exon 10. |
