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Rab23opb2
Chemically induced Allele Detail
Summary
Symbol: Rab23opb2
Name: RAB23, member RAS oncogene family; open brain 2
MGI ID: MGI:2137533
Synonyms: opb2
Gene: Rab23  Location: Chr1:33758968-33781645 bp, + strand  Genetic Position: Chr1, 12.8 cM
Alliance: Rab23opb2 page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU treatment induced a C-to-T mutation at position 238 of the encoded mRNA that altered codon 80 from an arginine to a stop codon (p.R80*). If the peptide is translated, it will lack the domains required for guanine nucleotide and Rab effector binding. (J:70423)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 97 assay results
1 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation: 6 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 Rab23 Mutation:  33 strains or lines available
References
Original:  J:48268 Kasarskis A, et al., A phenotype-based screen for embryonic lethal mutations in the mouse. Proc Natl Acad Sci U S A. 1998 Jun 23;95(13):7485-90
All:  14 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
04/16/2024
MGI 6.23
The Jackson Laboratory