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

Symbol:	Otop2m1J
Name:	otopetrin 2; mutation 1 Jackson
MGI ID:	MGI:5581450
Synonyms:	Otop3m1J, stiff
Gene:	Otop2  Location: Chr11:115197989-115223129 bp, + strand  Genetic Position: Chr11, 80.84 cM
Alliance:	Otop2m1J page

Strain of Origin:

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

Allele Type:    Spontaneous Mutation:    Single point mutation   Mutation details: This is a spontaneous G-to-A transition in the 3' UTR in chromosome 11 position 115,332,175 bp (GRCm38) that was identified in the same spontaneous mutant as the Fdxrm1J mutation. (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: 0 strains available      Cell Lines: 0 lines available
Carrying any Otop2 Mutation:	34 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)