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Allele : Kcnj2<tm1Llec> potassium inwardly-rectifying channel, subfamily J, member 2; targeted mutation 1, Lee L Eckhardt

Primary Identifier  MGI:6864155 Allele Type  Targeted
Attribute String  Conditional ready Gene  Kcnj2
Transmission  Germline Strain of Origin  129
Is Recombinase  false Is Wild Type  false
molecularNote  Using homologous recombination in the ES cells, R67Q mutation found in humans with exertion-induced polymorphic ventricular tachycardia (PMVT), bidirectional ventricular tachycardia (BiVT) and syncope was introduced into the Kcnj2 gene. The target vector contained R67Q-KCNJ2 with a neo cassette inserted into the primary sequence, flanked with loxP sites.
  • mutations:
  • Nucleotide substitutions
  • synonyms:
  • KCNJ2<R67Q-neo>,
  • KCNJ2<R67Q-neo>
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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