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Allele : Scn4b<tm1.2Geh> sodium channel, type IV, beta; targeted mutation 1.2, Gregg E Homanics

Primary Identifier  MGI:6155711 Allele Type  Targeted
Attribute String  Null/knockout Gene  Scn4b
Transmission  Germline Strain of Origin  (129X1/SvJ x 129S1/Sv)F1-Kitl<+>
Is Recombinase  false Is Wild Type  false
molecularNote  A targeting vector was designed to insert a loxP site, followed by a FRT-flanked neomycin resistance (neo) cassette, upstream of exon 2, and a second loxP site downstream of exon 2. Flp-mediated recombination removed the FRT-flanked neo cassette leaving exon 2 floxed. Cre-mediated recombination removed exon 2, which is predicted to cause a frameshift mutation resulting in a truncated product. Western blot analysis confirmed the absence of the 37 kD protein.
  • mutations:
  • Intragenic deletion
  • synonyms:
  • Scn4b KO,
  • Scn4b 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