| Primary Identifier | MGI:5425012 | Allele Type | Chemically induced (ENU) |
| Attribute String | Not Specified | Gene | Pmp22 |
| Strain of Origin | C3HeB/FeJ | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | This ENU-induced mutation was isolated in a screen for metabolic bone disease as part of the Munich ENU Mutagenesis Project. The molecular lesion is a mutation in exon 4 of the gene, altering nucleotide 206 from T-to-A in codon 69, predicted to result in an amino acid change from Methionine to Lysine (M69K). |
