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Allele : Kif5c<tm1.1Ics> kinesin family member 5C; targeted mutation 1.1, Mouse Clinical Institute

Primary Identifier  MGI:7616496 Allele Type  Targeted
Gene  Kif5c Transmission  Germline
Strain of Origin  C57BL/6NTac Is Recombinase  false
Is Wild Type  false
molecularNote  Glutamic acid codon 237 (GAA) in exon 8 was changed to valine (GTA) (p.E237V). A loxP site, a neomycin resistance gene cassette, an FRT site flanked auto-excision protamine-cre cassette and a second loxP site were inserted into intron 8. Loss-of-function mutations in the human ortholog are associated with complex cortical dysplasia with other brain malformations 2 (CDCBM2).
  • mutations:
  • Insertion,
  • Single point mutation
  • synonyms:
  • Kif5c<E237V>,
  • Kif5c<E237V>
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

3 Publication categories