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Allele : Iftap<tm1b(KOMP)Wtsi> intraflagellar transport associated protein; targeted mutation 1b, Wellcome Trust Sanger Institute

Primary Identifier  MGI:6356351 Allele Type  Targeted
Attribute String  Null/knockout, Reporter Gene  Iftap
Transmission  Germline Strain of Origin  C57BL/6N
Is Recombinase  false Is Wild Type  false
Project Collection  KOMP-CSD
molecularNote  The L1L2_gt0 cassette was inserted at position 101413619 of Chromosome 2 upstream of critical exon 5 (Build GRCm39). The cassette is composed of an FRT flanked lacZ/neomycin sequence followed by a loxP site. An additional loxP site is inserted downstream of exon 5 at position 101414384. Exon 5 is thus flanked by loxP sites. A reporter knockout allele was created by cre recombinase expression in mice carrying the parental Iftaptm1a(KOMP)Wtsi allele to remove loxP-flanked exon 5. RT-PCR and Western blot analysis confirmed the absence of full-length transcript and protein expression, respectively, in homozygous mutant testes. Further information on targeting strategies used for this and other IKMC alleles can be found at http://www.informatics.jax.org/mgihome/nomen/IKMC_schematics.shtml
  • mutations:
  • Insertion,
  • Intragenic deletion
  • synonyms:
  • NWC-KOMPcre,
  • NWC-KOMPcre,
  • NWC-KO,
  • NWC-KO
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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

5 Publication categories