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Allele : Samhd1<tm1d(EUCOMM)Wtsi> SAM domain and HD domain, 1; targeted mutation 1d, Wellcome Trust Sanger Institute

Primary Identifier  MGI:5551758 Allele Type  Targeted
Attribute String  Null/knockout Gene  Samhd1
Transmission  Germline Strain of Origin  C57BL/6N-A<tm1Brd>
Is Recombinase  false Is Wild Type  false
Project Collection  EUCOMM
molecularNote  The L1L2_Bact_P cassette was inserted at position 156971510 of Chromosome 2 upstream of the critical exon 2 (Build GRCm39). The cassette is composed of an FRT site followed by lacZ sequence and a loxP site. This first loxP site is followed by neomycin resistance gene under the control of the human beta-actin promoter, SV40 polyA, a second FRT site and a second loxP site. A third loxP site is inserted downstream of the targeted exon 2 at position 156972268. The critical exon 2 is thus flanked by loxP sites. Flp-mediated recombination removed the trapping cassette. Cre-mediated recombination removed exon 2. Western blot analysis confirmed the absence of protein expression in splenocytes.
  • mutations:
  • Intragenic deletion,
  • Insertion
  • synonyms:
  • SAMHD1<delta>,
  • SAMHD1<delta>
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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

9 Publication categories