| Primary Identifier | MGI:5424982 | Allele Type | Chemically induced (ENU) |
| Gene | Casr | 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. Missense mutation in exon 4 of the gene, a T-to-C point mutation at position 626 of the cDNA is predicted to alter codon 208 in the encoded protein from a valine to an alanine. |
