| Primary Identifier | MGI:7482339 | Allele Type | Targeted |
| Attribute String | Humanized sequence | Gene | Med23 |
| Transmission | Germline | Strain of Origin | Not Specified |
| Is Recombinase | false | Is Wild Type | false |
| molecularNote | A loxP flanked neomycin selection cassette and exon 17 containing an arginine to glutamine substitution at amino acid 617 (c.1850G>A, p.R617Q) replaced exon 17, which corresponds to c.1841G>A, p.R614Q in the mouse on GRCm39. The p.R617Q missense mutation was reported in a familial intellectual disability disorder. |
