Primary Identifier | MGI:1857079 | Allele Type | Spontaneous |
Attribute String | Null/knockout | Gene | Enpp1 |
Inheritance Mode | Recessive | Strain of Origin | Jcl:ICR |
Is Recombinase | false | Is Wild Type | false |
molecularNote | The genetic lesion responsible for this allele is a single base pair change(G>T) that changes glycine codon 568 into a stop codon (p.Gly568Ter). This leads to a premature truncation of the protein product that lacks a calcium binding site and the cysteine residues used in disulfide bonding. |