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Allele : Arhgap19<m1> Rho GTPase activating protein 19; mutation 1

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.
  • mutations:
  • Insertion
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

3 Publication categories

Trail: Allele