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Allele : Kcnv2<tm1.2(KOMP)Wtsi> potassium channel, subfamily V, member 2; targeted mutation 1.2, Wellcome Trust Sanger Institute

Primary Identifier  MGI:6382425 Allele Type  Targeted
Attribute String  Null/knockout Gene  Kcnv2
Transmission  Germline Strain of Origin  C57BL/6N-A<tm1Brd>
Is Recombinase  false Is Wild Type  false
Project Collection  KOMP-CSD
molecularNote  The L1L2_Del_BactPneo_FFL cassette was inserted at position 27396587 of Chromosome 19 upstream of exon 1 (Build 37). The cassette is composed of an FRT site followed by a neomycin resistance gene under the control of the human beta-actin promoter, SV40 polyA, a second FRT site and a loxP site. A second loxP site is inserted downstream of exon 1 at position 27398917. Exon 1 is thus flanked by loxP sites. Exon 1 was deleted through subsequent cre-mediated recombination.
  • mutations:
  • Intragenic deletion,
  • Insertion
  • synonyms:
  • Kcnv2<tm1b(KOMP)Wtsi>,
  • Kv8.2 KO,
  • Kv8.2 KO,
  • Kcnv2<tm1b(KOMP)Wtsi>
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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

4 Publication categories

Trail: Allele