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Allele : Scn1a<tm1.1Swl> sodium channel, voltage-gated, type I, alpha; targeted mutation 1.1, Shu-Wha Lin

Primary Identifier  MGI:5699848 Allele Type  Targeted
Attribute String  Null/knockout Gene  Scn1a
Transmission  Germline Strain of Origin  (129X1/SvJ x 129S1/Sv)F1-Kitl<+>
Is Recombinase  false Is Wild Type  false
molecularNote  A premature stop codon (CAG to TAG) at amino acid residue E1099 (E1099X) was introduced into the linker between domains 2 and 3. The loxP flanked neo cassette downstream of the mutation was removed via cre-mediated recombination. Western blot analysis indicates that global protein expression is reduced to 54.1% in heterozygotes and is undetectable in homozygotes, indicating a null allele.
  • mutations:
  • Single point mutation
  • synonyms:
  • Scn1a<E1099X>,
  • Scn1a<E1099X>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

4 Publication categories

Trail: Allele