| Primary Identifier | MGI:2656387 | Allele Type | Spontaneous |
| Gene | Szt1 | Inheritance Mode | Dominant |
| Strain of Origin | C57BL/6J | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | The Szt1 mutation represents a genomic deletion of about 300 kb of mouse chromosome 2. The deletion involves 3 known genes including those encoding the potassium channel, Kcnq2, and the nicotinic acetylcholine receptor subunit, Chrna4, and ADP-ribosylation factor GTPase activating protein 1, Arfgap1. |
