| Primary Identifier | MGI:1857838 | Allele Type | Spontaneous |
| Gene | Slc12a2 | Inheritance Mode | Recessive |
| Strain of Origin | MK/ReJ x C57BL/6J | Is Recombinase | false |
| Is Wild Type | false |
| description | This allele fails to complement the sy locus but does complement the fused plalanges alleles. Therefore, the original sy deletion includes both the gene responsible for deafness (Slc12a2) and the gene responsible for abnormal foot morphology. |
| molecularNote | Nucleotide insertion at position 2955 located in exon 21 causes a frameshift and a premature stop codon. |
