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Allele : Scn1b<tm1.1Bion> sodium channel, voltage-gated, type I, beta; targeted mutation 1.1, Bionomics Limited

Primary Identifier  MGI:4829975 Allele Type  Targeted
Attribute String  Humanized sequence Gene  Scn1b
Transmission  Germline Strain of Origin  Not Specified
Is Recombinase  false Is Wild Type  false
molecularNote  Exon 3 was replaced with one in which a C to G transversion (C387G) results in the amino acid substitution of tryptophan for cysteine at position 121 (C121W), mimicking a mutation found in some genetic epilepsy with febrile seizures plus (GEFS+) patients. A loxP was inserted upstream of the modified exon 3. A floxed neo cassette inserted downstream of the modified exon was removed by cre mediated recombination. The modified exon 3 remains floxed.
  • mutations:
  • Single point mutation,
  • Insertion
  • synonyms:
  • Scn1b<W>,
  • beta1<C121W>,
  • beta1<C121W>,
  • Scn1b<W>
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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

6 Publication categories

Trail: Allele