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Allele : Scn10a<tm1.1Yah> sodium channel, voltage-gated, type X, alpha; targeted mutation 1.1, Yann Herault

Primary Identifier  MGI:7564596 Allele Type  Targeted
Attribute String  Humanized sequence Gene  Scn10a
Transmission  Germline Strain of Origin  C57BL/6NCrl
Is Recombinase  false Is Wild Type  false
molecularNote  Glycine codon 1663 (GGC) in exon 28 was changed to serine (AGC) (p.G1663S) and a loxP site, a neomycin resistance gene cassette, a cre gene cassette and a second loxP site were inserted into intron 27. The neo and cre cassettes auto-excised. The mutation is the equivalent of the human p.G1662S gain-of-function mutation associated with idiopathic painful small fiber neuropathy (SFN).
  • mutations:
  • Insertion,
  • Single point mutation
  • synonyms:
  • Scn10a<G1663S>,
  • Scn10a<G1663S>
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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

3 Publication categories

Trail: Allele