Primary Identifier | MGI:5297958 | Allele Type | Spontaneous |
Gene | Arhgap19 | Strain of Origin | BALB/cCrl |
Is Recombinase | false | Is Wild Type | false |
molecularNote | A single T nucleotide insertion is located at position 945 in exon 6 (945T) creating a frameshift mutation resulting in a truncated protein due to a premature stop codon at the end of exon 6 at position 309 (K309*). This mutation is unique to BALB/cCrl and BALB/cAnNCrl strains and is not found in BALB/cJ derived strains. |