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Fdxrm1J
Spontaneous Allele Detail
Nomenclature
Symbol: Fdxrm1J
Name: ferredoxin reductase; mutation 1 Jackson
MGI ID: MGI:5581449
Synonyms: FdxrR389Q, stiff
Gene: Fdxr  Location: Chr11:115268024-115277050 bp, - strand  Genetic Position: Chr11, 80.84 cM, cytoband E2
Mutation
origin
Mutation
description
Allele Type:    Spontaneous (Hypomorph)
Mutation:    Single point mutation
 
Mutation detailsThis spontaneous C-to-T transition at chromosome 11 position 115,269,462 bp (GRCm38) causes a p.R389Q substitution and was identified in the same spontaneous mutant mouse as Otop3m1J. (J:222308)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Fdxr Mutation:  15 strains or lines available
References
Original:  J:223793 Dionne LA, et al., Stiffened hindquarters, a new spontaneous mutation. MGI Direct Data Submission. 2015;
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
04/13/2021
MGI 6.16
The Jackson Laboratory