| Primary Identifier | MGI:2386682 | Allele Type | Spontaneous |
| Gene | Sharpin | Inheritance Mode | Recessive |
| Strain of Origin | OcB3/Dem | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | This allele comprises a C-to-A transition at coding nucleotide 15 near the 5' end of exon 1 (a silent mutation that doesn't change the alanine codon at position 5), followed by a 14 bp deletion of coding nucleotides 19-32. The deletion disrupts the reading frame resulting in a premature stop codon. |
