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Allele : Timm22<tm1b(KOMP)Wtsi> translocase of inner mitochondrial membrane 22; targeted mutation 1b, Wellcome Trust Sanger Institute

Primary Identifier  MGI:5529629 Allele Type  Targeted
Attribute String  Null/knockout, Reporter Gene  Timm22
Transmission  Germline Strain of Origin  C57BL/6N
Is Recombinase  false Is Wild Type  false
Project Collection  KOMP-CSD
molecularNote  The L1L2_gt1 cassette was inserted at position 76300011 of Chromosome 11 upstream of the critical exon(s) (Build GRCm39). The cassette is composed of an FRT flanked lacZ/neomycin sequence followed by a loxP site. An additional loxP site was inserted downstream of the targeted exon(s) at position 76300952. The critical exon(s) were thus flanked by loxP sites, and subsequent Cre-mediated excision deleted the critical sequence and the neomycin selection cassette yielding a knockout reporter construct. 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:
  • Timm22<->,
  • Timm22<->
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

0 Driven By

11 Publication categories