Primary Identifier | MGI:3766915 | Allele Type | Spontaneous |
Gene | Adamts20 | Inheritance Mode | Recessive |
Strain of Origin | Not Specified | Is Recombinase | false |
Is Wild Type | false |
molecularNote | Complemetation testing demonstrated allelism between this mutation and Adamts20bt-Bei1. Sequence analysis identified the molecular lesion as a a C-to-T transition at nucleotide position 2451 (NM_177431.5:c.2281C>T), which is predicted to replace a highly-conserved leucine in the protein's spacer domain with phenylalanine (L761F). |