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Raratm3.1Ipc
Targeted Allele Detail
Summary
Symbol: Raratm3.1Ipc
Name: retinoic acid receptor, alpha; targeted mutation 3.1, Pierre Chambon
MGI ID: MGI:2386107
Synonyms: RARalpha L-
Gene: Rara  Location: Chr11:98818644-98865768 bp, + strand  Genetic Position: Chr11, 62.76 cM, cytoband D-E1
Alliance: Raratm3.1Ipc page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:75135
Parent Cell Line:  D4 (ES Cell)
Strain of Origin:  129/Sv
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsThe floxed fragment containing exon 8 was excised from Raratm3Ipc by mating with mice carrying Tg(CMV-cre)1Ipc . The deletion eliminated the majority of the DNA binding domain and introduced a frameshift mutation. A lack of protein expression was demonstrated in homozygous mutant mice via immunohistochemical analysis of testis sections. (J:75135)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 1 RNA-Seq or microarray experiment(s)
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 Rara Mutation:  79 strains or lines available
References
Original:  J:75135 Chapellier B, et al., A conditional floxed (loxP-flanked) allele for the retinoic acid receptor alpha (RARalpha) gene. Genesis. 2002 Feb;32(2):87-90
All:  10 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