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Allele : Cep290<tm2.1Rwjc> centrosomal protein 290; targeted mutation 2.1, Robert WJ Collin

Primary Identifier  MGI:5578357 Allele Type  Targeted
Attribute String  Humanized sequence, Inserted expressed sequence Gene  Cep290
Transmission  Germline Strain of Origin  129S2/SvPas
Is Recombinase  false Is Wild Type  false
molecularNote  Exons 25 and 26 were replaced with the sequence for human exon 26 and 27 with the deep intronic Leber Congenital Amaurosis-causing mutation (c.2991+1655AG). Cre-mediated recombination removed a floxed neomycin resistance cassette inserted downstream of human exon 27.
  • mutations:
  • Intragenic deletion,
  • Insertion
  • synonyms:
  • Cep290<lca>,
  • Cep290<lca>
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1 Feature

Genome

1 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

4 Publication categories