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Vsx1tm1Bhr
Targeted Allele Detail
Summary
Symbol: Vsx1tm1Bhr
Name: visual system homeobox 1; targeted mutation 1, Richard R Behringer
MGI ID: MGI:3040317
Synonyms: Vsx1-
Gene: Vsx1  Location: Chr2:150522622-150531057 bp, - strand  Genetic Position: Chr2, 74.74 cM
Alliance: Vsx1tm1Bhr page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:89292
Parent Cell Line:  PC3 (ES Cell)
Strain of Origin:  129S4/SvJae-Tg(Prm-cre)70Og
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsTargeting took place in ES cells carrying a cre transgene Tg(Prm-cre)70Og, which expresses Cre recombinase under control of the male-germline specific protamine promoter. A floxed neo cassette replaced the coding region for the entire homeodomain and CVC domain, leaving fragments of exons 1 and 5 intact. Cre-mediated excision removed the neo cassette upon transmission from male chimeras. (J:89292)
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 Vsx1 Mutation:  10 strains or lines available
References
Original:  J:89292 Ohtoshi A, et al., Regulation of retinal cone bipolar cell differentiation and photopic vision by the CVC homeobox gene Vsx1. Curr Biol. 2004 Mar 23;14(6):530-6
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
04/23/2024
MGI 6.23
The Jackson Laboratory