Summary | Mutation origin | Mutation description | Phenotypes | Disease models | Find Mice (IMSR) | References

Symbol:	Fdxrm1J
Name:	ferredoxin reductase; mutation 1 Jackson
MGI ID:	MGI:5581449
Synonyms:	FdxrR389Q, stiff
Gene:	Fdxr  Location: Chr11:115158850-115167876 bp, - strand  Genetic Position: Chr11, 80.84 cM, cytoband E2
Alliance:	Fdxrm1J page

Strain of Origin:

B6;129S-Gt(ROSA)26Sortm38(CAG-GCaMP3)Hze/J

Allele Type:    Spontaneous (Hypomorph) Mutation:    Single point mutation   Mutation details: This 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

View phenotypes and curated references for all genotypes (concatenated display).

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:	22 strains or lines available

Original:	J:223793 Dionne LA, et al., Stiffened hindquarters, a new spontaneous mutation. MGI Direct Data Submission. 2015;
All:	3 reference(s)