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Allele : Hells<tm1d(EUCOMM)Wtsi> helicase, lymphoid specific; targeted mutation 1d, Wellcome Trust Sanger Institute

Primary Identifier  MGI:6389563 Allele Type  Targeted
Attribute String  Null/knockout Gene  Hells
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 38939858 of Chromosome 19 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 38940603. The critical exon(s) was thus flanked by loxP sites and a "conditional ready" (floxed) tm1c allele was created by flp recombinase expression in mice carrying this allele to remove the lacZ sequence and neomycin selection cassette, and subsequent breeding to a cre-deleter removed the critical exon(s) yielding this null allele.
  • mutations:
  • Intragenic deletion
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

0 Driven By

5 Publication categories