| Primary Identifier | MGI:3819772 | Allele Type | Targeted |
| Attribute String | Conditional ready, No functional change | Gene | Uqcrfs1 |
| Transmission | Germline | Strain of Origin | Not Specified |
| Is Recombinase | false | Is Wild Type | false |
| description | Phenotypic Similarity to Human Syndrome: Mitochondrial Complex III Deficiency in homozygous mice carrying Tg(Camk2a-cre)#Szi (J:188773) |
| molecularNote | The exon 2 was flanked by loxP sites and a neomycin/thymidine kinase cassette was inserted in the 3' untranslated region via homologous recombination. Western blot analysis detected decreased protein levels in skin but not muscle, heart, brain or liver from homozygotes. |
