Primary Identifier | MGI:7495802 | Allele Type | Endonuclease-mediated |
Attribute String | Humanized sequence | Gene | Ighmbp2 |
Inheritance Mode | Semidominant | Strain of Origin | C57BL/6J |
Is Recombinase | false | Is Wild Type | false |
molecularNote | This A to G point mutation (c.2753A>G) changes amino acid 918 from tyrosine to cysteine, replicating the Tyr920Cys disease-causing mutation found in human. |