| Primary Identifier | MGI:2651859 | Allele Type | Spontaneous |
| Attribute String | Modified isoform(s) | Gene | Ush1c |
| Inheritance Mode | Recessive | Strain of Origin | B6;129S4-Add2<tm1Llp> |
| Is Recombinase | false | Is Wild Type | false |
| molecularNote | The dfcr-2J mutation has been identified as the deletion of a single base pair, the fourth nucleotide in the inner ear-specific exon C of the 28-exon Ush1c gene. This shifts the translational reading frame shift so that 38 incorrect amino acids are incorporated before a premature stop codon is encountered. |
