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Allele : Rpe65<tm1Lrcb> retinal pigment epithelium 65; targeted mutation 1, Christian Grimm

Primary Identifier  MGI:3771723 Allele Type  Targeted
Gene  Rpe65 Transmission  Germline
Strain of Origin  129S6/SvEvTac Is Recombinase  false
Is Wild Type  false
molecularNote  Two point mutations were introduced into exon 4 at codon 91 (CGA to TGG) to cause an arginine to tryptophan missense mutation (R91W). A floxed neomycin resistance cassette was also introduced into intron 6 for targeting purposes. Founder mice were mated with deleter mice to remove the neomycin cassette, leaving behind a single loxP site. Levels of the mutant protein are reduced by 95% compared to wild-type controls as determined by western blots of retinal extracts.
  • mutations:
  • Insertion
  • synonyms:
  • R91W,
  • Rpe65<R91W>,
  • Rpe65<R91W>,
  • R91W
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

Trail: Allele

0 Driven By

23 Publication categories

Trail: Allele