| Primary Identifier | MGI:2154359 | Allele Type | Targeted |
| Attribute String | Null/knockout, Reporter | Gene | Hnf1a |
| Transmission | Germline | Strain of Origin | 129S2/SvPas |
| Is Recombinase | false | Is Wild Type | false |
| description | ES cell line = CK11 Phenotypic Similarity to Human Syndrome: Fanconi Renotubular Syndrome (J:31627) |
| molecularNote | A cassette containing nls-lacZ and neo was inserted at the start codon, resulting in the deletion of sequence encoding 108 residues comprising the entire dimerization domain and a portion of the B domain, as well as the majority of intron 1. Expression of beta-galactosidase was observed via Xgal staining. |
