| Primary Identifier | MGI:5515368 | Allele Type | Chemically induced (ENU) |
| Attribute String | Null/knockout | Gene | Smarcc1 |
| Inheritance Mode | Dominant | Strain of Origin | FVB/N |
| Is Recombinase | false | Is Wild Type | false |
| molecularNote | A T-to-G single point mutation in the exon 10 splice acceptor site is predicted to result in a splicing defect in the mRNA. The encoded protein was not detected on Western blot of embryonic tissue, suggesting that this allele is null. |
