| Primary Identifier | MGI:5446796 | Allele Type | Targeted |
| Attribute String | Humanized sequence | Gene | Bcs1l |
| Transmission | Germline | Strain of Origin | 129 |
| Is Recombinase | false | Is Wild Type | false |
| molecularNote | Exon 2 was replaced with a modified exon 2, which contains a nucleotide substitution of A to G causing an S78G amino acid change, mimicking the mutation causing the autosomal recessive GRACILE syndrome in human. Cre-mediated recombination removed the floxed neo cassette inserted upstream of the modified exon 2. |
