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Allele : Cdc27<tm1.1Ics> cell division cycle 27; targeted mutation 1.1, Mouse Clinical Institute

Primary Identifier  MGI:7616486 Allele Type  Targeted
Attribute String  Conditional ready, Humanized sequence Gene  Cdc27
Transmission  Germline Strain of Origin  C57BL/6NTac
Is Recombinase  false Is Wild Type  false
molecularNote  Serine codon 93 (TCT) in exon 4 was changed to phenylalanine (TTT) (p.S93F). A loxP site was inserted into intron 3 and an FRT site flanked neomycin resistance gene cassette and second loxP site were inserted into intron 5. The neo cassette was removed through subsequent Flp-mediated recombination, leaving exons 4-5 floxed. Mutations in the human ortholog are associated with non-syndromic intellectual disability.
  • mutations:
  • Single point mutation,
  • Insertion
  • synonyms:
  • Cdc27<S92F>,
  • Cdc27<S92F>
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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

3 Publication categories

Trail: Allele