| Primary Identifier | MGI:1856620 | Allele Type | Spontaneous |
| Gene | olt | Inheritance Mode | Recessive |
| Strain of Origin | C3H/HeJOrl | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | This phenotypic mutation has been localized to chromosome 9 distal to D9Mit279. Nucleotide 118,855,090 is joined to 119,089,970 (Build 37) indicating that this is a 234 kb deletion. The deletion region contains Vill, Plcd1, Dlec1, Acaa1b, and parts of Ctdspl and Slc22a14. |
