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Allele : Ift25<tm1b(EUCOMM)Wtsi> intraflagellar transport 25; targeted mutation 1b, Wellcome Trust Sanger Institute

Primary Identifier  MGI:5426875 Allele Type  Targeted
Attribute String  Null/knockout, Reporter Gene  Ift25
Transmission  Germline Strain of Origin  C57BL/6N
Is Recombinase  false Is Wild Type  false
Project Collection  EUCOMM
molecularNote  The L1L2_gt2 cassette was inserted at position 106945715 of Chromosome 4 upstream of the critical exon(s) (Build 37). The cassette is composed of an FRT flanked lacZ/neomycin sequence followed by a loxP site. An additional loxP site is inserted downstream of the targeted exon(s) at position 106946668. The critical exon(s) is/are thus flanked by loxP sites. Cre mediated recombination deleted exon 3. Western blot analysis confirmed the absence of protein expression in homozygous mice.
  • mutations:
  • Insertion,
  • Intragenic deletion
  • synonyms:
  • Ift25<null1>,
  • Ift25<null1>
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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

6 Publication categories