Primary Identifier | MGI:6114639 | Allele Type | Chemically induced (ENU) |
Attribute String | Not Specified | Gene | Prkdc |
Inheritance Mode | Dominant | 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 15,719,433 (v38) on chromosome 16, or base pair 81,991 in the GenBank genomic region NC_000082. The mutation corresponds to residue 5,170 in the mRNA sequence NM_011159 within exon 39 of 86 total exons. The mutation results in a valine (V) to alanine (A) substitution at position 1716 (V1716A) in the protein. |