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Raxtm1.2Lwd
Targeted Allele Detail
Summary
Symbol: Raxtm1.2Lwd
Name: retina and anterior neural fold homeobox; targeted mutation 1.2, Mark Lewandoski
MGI ID: MGI:3576779
Synonyms: Rxdelta2
Gene: Rax  Location: Chr18:66067710-66072160 bp, - strand  Genetic Position: Chr18, 39.03 cM
Alliance: Raxtm1.2Lwd 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 (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsCrossing Raxtm1Lwd mice with cre-deleter mice removed exon 2 in the germ line, leaving exon 3 out of frame and causing the creation of a truncated, nonfunctional protein lacking the homeodomain. (J:97314)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 anatomical structure(s)
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:  3 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
10/22/2024
MGI 6.24
The Jackson Laboratory