| Primary Identifier | MGI:7616481 | Allele Type | Targeted |
| Attribute String | Conditional ready, No functional change | Gene | Wdr62 |
| Transmission | Germline | Strain of Origin | C57BL/6NTac |
| Is Recombinase | false | Is Wild Type | false |
| molecularNote | A loxP site was inserted into intron 3 and an FRT site flanked neomycin resistance gene cassette and second loxP site were inserted into intron 7. The neo cassette was removed through subsequent Flp-mediated recombination, leaving exons 4-7 floxed. Loss-of-function mutations in the human ortholog are associated with autosomal recessive primary microcephaly 2 with or without cortical malformations. |
