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Allele : Crx<em2Smgc> cone-rod homeobox; endonuclease-mediated mutation 2, Shiming Chen

Primary Identifier  MGI:7576954 Allele Type  Endonuclease-mediated
Attribute String  Humanized sequence Gene  Crx
Strain of Origin  C57BL/6J Is Recombinase  false
Is Wild Type  false
molecularNote  Lysine codon 88 (AAG) in exon 4 was changed to asparagine (AAC) (p.K88N) using an sgRNA and an ssODN template with CRISPR/Cas9 technology. The mutation, in the homeodomain (HD) of the encoded peptide, is the equivalent of same human mutation associated with dominant Leber congenital amaurosis 7 (LCA7).
  • mutations:
  • Single point mutation
  • synonyms:
  • Crx<K88N>,
  • Crx<K88N>
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

0 Driven By

3 Publication categories