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Raratm1Ipc
Targeted Allele Detail
Summary
Symbol: Raratm1Ipc
Name: retinoic acid receptor, alpha; targeted mutation 1, Pierre Chambon
MGI ID: MGI:1857622
Synonyms: Aalpha, Rara-, RARalpha-
Gene: Rara  Location: Chr11:98818644-98865768 bp, + strand  Genetic Position: Chr11, 62.76 cM, cytoband D-E1
Alliance: Raratm1Ipc page
Degenerative lesions in testes of 4 to 5 month old Raratm1Ipc/Raratm1Ipc mice

Show the 1 phenotype image(s) involving this allele.

Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:13574
Parent Cell Line:  D3 (ES Cell)
Strain of Origin:  129S2/SvPas
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Insertion
 
Mutation detailsA neomycin cassette was inserted into exon 8, which encodes the common receptor region B. This disruption is predicted to prevent the synthesis of all Rara isoforms. RNAase protection analysis of homozygous E13.5 embryos failed to detect wild type RNA transcripts and immunoblot analysis failed to detect protein in in extracts from homozygous E13.5 embryos. (J:13574)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 128 assay results
In Structures Affected by this Mutation: 21 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:13574 Lufkin T, et al., High postnatal lethality and testis degeneration in retinoic acid receptor alpha mutant mice. Proc Natl Acad Sci U S A. 1993 Aug 1;90(15):7225-9
All:  32 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