| Primary Identifier | MGI:6116661 | Allele Type | Targeted |
| Gene | Umod | Transmission | Germline |
| Strain of Origin | (129X1/SvJ x 129S1/Sv)F1-Kitl<+> | Is Recombinase | false |
| Is Wild Type | false |
| description | Phenotypic Similarity to Human Syndrome: autosomal dominant tubulointerstitial kidney disease J:242593. |
| molecularNote | Homologous recombination introduced the C125R mutation in exon 3 and a loxP flanked neomycin resistance cassette in intron 2. The floxed neomycin cassette was removed via Cre-mediated recombination. The C125R mutation alters the third cysteine residue of the calcium-binding epidermal growth factor-like domain 3. |
