| Primary Identifier | MGI:2138070 | Allele Type | Targeted |
| Attribute String | Null/knockout | Gene | Lamb2 |
| 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: human congenital or idiopathic nephritic syndromes such as minimal change nephrotic syndrome (MCNS) and glomerulonephrosis (J:27732). |
| molecularNote | Insertion of a neomycin cassette into the second exon of the gene. |
