Primary Identifier | MGI:5578357 | Allele Type | Targeted |
Attribute String | Humanized sequence, Inserted expressed sequence | Gene | Cep290 |
Transmission | Germline | Strain of Origin | 129S2/SvPas |
Is Recombinase | false | Is Wild Type | false |
molecularNote | Exons 25 and 26 were replaced with the sequence for human exon 26 and 27 with the deep intronic Leber Congenital Amaurosis-causing mutation (c.2991+1655AG). Cre-mediated recombination removed a floxed neomycin resistance cassette inserted downstream of human exon 27. |