| Primary Identifier | MGI:4456247 | Allele Type | Chemically induced (ENU) |
| Gene | Atp11c | Inheritance Mode | Not Specified |
| Strain of Origin | C57BL/6JApb | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | This mutation comprises a G to A transition in intron 27 (genomic position 57,491,646 of ENSMUSG00000062949) that alters the intron/exon boundary splice site. |