Primary Identifier | MGI:6108106 | Allele Type | Chemically induced (ENU) |
Attribute String | Hypomorph | Gene | Hcfc2 |
Strain of Origin | C57BL/6J | Is Recombinase | false |
Is Wild Type | false |
molecularNote | ENU mutagenesis induced a T to A point mutation that results in the amino acid substitution of isoleucine for phenylalanine at position 599 (F599I). |