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Allele : Caprin2<tm2a(EUCOMM)Wtsi> caprin family member 2; targeted mutation 2a, Wellcome Trust Sanger Institute

Primary Identifier  MGI:4434168 Allele Type  Targeted
Attribute String  Conditional ready, Null/knockout, Reporter Gene  Caprin2
Transmission  Germline Strain of Origin  C57BL/6N
Is Recombinase  false Is Wild Type  false
Project Collection  EUCOMM
description  Phenotypic Similarity to Human Syndrome: Peters Anomaly in homozygous mice carrying Tg(Pax6-GFP/cre)1Rilm (J:225905)
molecularNote  The L1L2_gt0 cassette was inserted at position 148778960 of Chromosome 6 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 is inserted downstream of the targeted exon(s) at position 148779938. The critical exon(s) is/are thus flanked by loxP sites. A "conditional ready" (floxed) allele can be created by flp recombinase expression in mice carrying this allele. Subsequent cre expression results in a knockout mouse. If cre expression occurs without flp expression, a reporter knockout mouse will be created. 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
  • synonyms:
  • Caprin2<flox>,
  • Caprin2<flox>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

Trail: Allele

0 Driven By

7 Publication categories

Trail: Allele