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Raxtm1.1Lwd
Targeted Allele Detail
Summary
Symbol: Raxtm1.1Lwd
Name: retina and anterior neural fold homeobox; targeted mutation 1.1, Mark Lewandoski
MGI ID: MGI:3576778
Synonyms: Rxflox
Gene: Rax  Location: Chr18:66067710-66072160 bp, - strand  Genetic Position: Chr18, 39.03 cM
Alliance: Raxtm1.1Lwd page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:97314
Parent Cell Line:  W9.5/W95 (ES Cell)
Strain of Origin:  129S1/Sv-Oca2+ Tyr+ Kitl+
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
 
Mutation detailsCrossing Raxtm1Lwd with mice expressing FLP recombinase removed the FRT-flanked neo in intron 1, while exon 2 remained flanked by loxP sites. (J:97314)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 38 assay results
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 Rax Mutation:  16 strains or lines available
References
Original:  J:97314 Voronina VA, et al., Conditional alleles for activation and inactivation of the mouse Rx homeobox gene. Genesis. 2005 Apr;41(4):160-4
All:  7 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
10/29/2024
MGI 6.24
The Jackson Laboratory