| Primary Identifier | MGI:7616390 | Allele Type | Targeted |
| Attribute String | Conditional ready, No functional change | Gene | Med23 |
| Transmission | Germline | Strain of Origin | C57BL/6NCrl |
| 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 4. The neo cassette was removed through subsequent Flp-mediated recombination, leaving exon 4 floxed. Mutations in the human ortholog are associated with autosomal recessive intellectual disability 18. |
