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Kcnk7tm1(KOMP)Vlcg
Targeted Allele Detail
Summary
Symbol: Kcnk7tm1(KOMP)Vlcg
Name: potassium channel, subfamily K, member 7; targeted mutation 1, Velocigene
MGI ID: MGI:3812821
Synonyms: Kcnk7tm1Vlcg
Gene: Kcnk7  Location: Chr19:5754395-5757137 bp, + strand  Genetic Position: Chr19, 4.34 cM, cytoband B2
IMPC: Kcnk7 gene page
Mutation
origin
Mutant Cell Lines:  11022A-A2, 11022A-A11, 11022A-B9
Germline Transmission:  Unknown
Parent Cell Line:  VGB6 (ES Cell)
Strain of Origin:  C57BL/6NTac
Project Collection: KOMP-Regeneron
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutations:    Insertion, Intragenic deletion     Vector: ZEN-Ub1
 
Mutation detailsThe insertion of Velocigene cassette ZEN-Ub1 created a deletion of size 2563bp between positions 5754487-5757049 of Chromosome 19 (Build GRCm39). (J:136110)
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: 1 line available
Carrying any Kcnk7 Mutation:  19 strains or lines available
References
Original:  J:136110 Velocigene, Alleles produced for the KOMP project by Velocigene (Regeneron Pharmaceuticals). MGI Direct Data Submission. 2008;
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
04/16/2024
MGI 6.23
The Jackson Laboratory