| Primary Identifier | MGI:1856929 | Allele Type | Chemically induced (ENU) |
| Gene | Dsg4 | Inheritance Mode | Recessive |
| Strain of Origin | NB | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | The mutation in the lah allele was identified as an A to C transversion at nucleotide 587 within exon 6. The mutation causes a tyrosine to serine change at amino acid position 196 affecting a potential phosphorylation site. |
