| Primary Identifier | MGI:2661962 | Allele Type | Spontaneous |
| Gene | Ncf1 | Inheritance Mode | Recessive |
| Strain of Origin | B6.Cg-Dock7<m> +/+ Lepr<db>/J | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | The mutation is an A-to-C transversion at the -2 position 5' off exon 8 in intron 7, changing splice acceptor site CAG to CCG. This results in aberrant splicing of the transcript. Immunoblotting detected no intact NCF1 protein in cells from these mice. |
