| Primary Identifier | MGI:5056365 | Allele Type | Chemically induced (ENU) |
| Gene | Grhl2 | Strain of Origin | A/J |
| Is Recombinase | false | Is Wild Type | false |
| molecularNote | Identified in an ENU screen and mapped to Chromosome 15 0-73 (4 Mb). The mutation is an A-to-G coding change in the eleventh exon of the Grhl2 locus (c.A1451G; p.D484G, genomic position chr15:37,336,311 GRCm38) |
