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Allele : Kcnn2<m1Btlr> potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2; mutation 1, Bruce Beutler

Primary Identifier  MGI:3800578 Allele Type  Chemically induced (ENU)
Gene  Kcnn2 Inheritance Mode  Recessive
Strain of Origin  C57BL/6J Is Recombinase  false
Is Wild Type  false Project Collection  Beutler Mutagenetix
molecularNote  This mutation, whose phenotype was first observed among G3 progeny of an ENU-mutagenized male mouse, has been identified as a T to C transition at nucleotide 503 of this gene, in the third of its 9 exons. This substitution is predicted to result in replacement of leucine by proline at amino acid position 168 of the standard form of the protein, which corresponds to amino acid position 443 of the long protein isoform, in the second transmembrane helix. Expression has not been analyzed.
  • mutations:
  • Single point mutation
  • synonyms:
  • jitter,
  • jitter
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

0 Driven By

3 Publication categories