| Primary Identifier | MGI:5817460 | Allele Type | Chemically induced (ENU) |
| Attribute String | Not Specified | Gene | Scube3 |
| Inheritance Mode | Recessive | Strain of Origin | C3HeB/FeJ |
| Is Recombinase | false | Is Wild Type | false |
| description | Phenotypic Similarity to Human Syndrome: Paget disease of the bone 1 J: 237904. |
| molecularNote | A C-to-A transversion at nucleotide position 882 in exon 8 leads to an asparagine to lysine exchange at protein position 294 (N294K). |
