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Rdh10trex
Chemically induced Allele Detail
Summary
Symbol: Rdh10trex
Name: retinol dehydrogenase 10 (all-trans); trex
MGI ID: MGI:4437845
Synonyms: trex
Gene: Rdh10  Location: Chr1:16176106-16202774 bp, + strand  Genetic Position: Chr1, 4.94 cM
Alliance: Rdh10trex page
Short forelimbs in E9.5-E10.5 Rdh10trex/Rdh10trex embryos

Show the 5 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  129S1/Sv or C57BL/6
Mutation
description
Allele Type:    Chemically induced (ENU) (Hypomorph)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a T to C transition at nucleotide 251 (NM_133832) that results in the amino acid substitution of arginine for cystinine. This mutation is predicted to disrupt the first beta strand of the protein. Residual Retinoic Acid signaling is detected in the trunk neural tube indicating this is a severely hypomorphic allele. (J:121229, J:185330)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 36 assay results
1 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation: 41 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 Rdh10 Mutation:  20 strains or lines available
References
Original:  J:121229 Sandell LL, et al., RDH10 is essential for synthesis of embryonic retinoic acid and is required for limb, craniofacial, and organ development. Genes Dev. 2007 May 1;21(9):1113-24
All:  9 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
11/19/2024
MGI 6.24
The Jackson Laboratory