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Kcnv2tm1.1(KOMP)Wtsi
Targeted Allele Detail
Summary
Symbol: Kcnv2tm1.1(KOMP)Wtsi
Name: potassium channel, subfamily V, member 2; targeted mutation 1.1, Wellcome Trust Sanger Institute
MGI ID: MGI:5586809
Synonyms: Kcnv2tm1c(KOMP)Wtsi
Gene: Kcnv2  Location: Chr19:27299988-27314579 bp, + strand  Genetic Position: Chr19, 21.88 cM
Alliance: Kcnv2tm1.1(KOMP)Wtsi page
IMPC: Kcnv2 gene page
Mutation
origin
Mutant Cell Line:  EPD0600_3_B03
Germline Transmission:  Earliest citation of germline transmission: J:82809
Parent Cell Line:  JM8A3.N1 (ES Cell)
Strain of Origin:  C57BL/6N-Atm1Brd
Project Collection: KOMP-CSD
Mutation
description
Allele Type:    Targeted (Conditional ready)
Mutation:    Insertion     Vector: L1L2_Del_BactPneo_FFL
 
Mutation detailsThis conditional allele was derived by flp recombinase from Kcnv2tm1(KOMP)Wtsi. The FRT site-flanked selection cassette has been deleted, leaving the critical exon flanked by loxP sites. (J:82809)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Kcnv2 Mutation:  24 strains or lines available
References
Original:  J:82809 European Mouse Mutant Archive, Information obtained from the European Mouse Mutant Archive (EMMA). Unpublished. 2003-2013;
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory