| Primary Identifier | MGI:3813487 | Allele Type | Spontaneous |
| Gene | Ppp1r13l | Inheritance Mode | Recessive |
| Strain of Origin | BALB/cJ | Is Recombinase | false |
| Is Wild Type | false |
| description | Phenotypic Similarity to Human Syndrome: novel autosomal recessive cardio-cutaneous syndrome (J:264272). |
| molecularNote | The underlying mutation is a 4 base pair deletion in exon 12. |
