| Primary Identifier | MGI:1856502 | Allele Type | Spontaneous |
| Gene | Foxn1 | Inheritance Mode | Recessive |
| Strain of Origin | 101/HY | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | A point mutation resulting in the C-to-T transition at nucleotide 1051 (accession# X81593) located in exon 7, leads to the replacement of an arginine with a cysteine at amino acid 320 (p.R320C). Although mutant protein is detectable in the nucleus, there was no detectable activation of the Krt2-18 target gene. |
