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Allele : Scn8a<5J> sodium channel, voltage-gated, type VIII, alpha; 5 Jackson

Primary Identifier  MGI:2183472 Allele Type  Chemically induced (ENU)
Gene  Scn8a Inheritance Mode  Recessive
Strain of Origin  C57BL/6J Is Recombinase  false
Is Wild Type  false
molecularNote  This phenotypic mutant was identified in an ENU mutagenesis screen. A complementation test between nmf5 and C3HeB/FeJ-Scn8amed-J revealed that nmf5 is a new allele of Scn8a. Molecular sequence analysis revealed that an A-to-T transversion mutation had occurred that is predicted to change the amino acid isoleucine 1392 to phenylalanine in the encoded protein. This conserved residue is within the S5-S6 pore loop of transmembrane domain 3.
  • mutations:
  • Single point mutation
  • synonyms:
  • Scn8a<nmf5>,
  • Scn8a<nmf5>,
  • nmf5,
  • neuroscience mutagenesis facility, 5,
  • NMF5,
  • NMF5,
  • nmf5,
  • neuroscience mutagenesis facility, 5
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

0 Driven By

5 Publication categories