Primary Identifier | MGI:6199962 | Allele Type | Chemically induced (ENU) |
Attribute String | Not Specified | Gene | Prkcd |
Inheritance Mode | Semidominant | Strain of Origin | C57BL/6J |
Is Recombinase | false | Is Wild Type | false |
Project Collection | Beutler Mutagenetix |
molecularNote | ENU-induced T to C transition at base pair 30,610,301 (v38) on chromosome 14, or base pair 16,114 in the GenBank genomic region NC_000080 encoding Prkcd. The mutation corresponds to residue 10 in the mRNA sequence NM_001310682 within exon 1 of 17 total exons. The mutation results in a methionine to threonine substitution at position 1 (M1T) in the PRKCD protein. |