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

Symbol:	Myo7ash1-13J
Name:	myosin VIIA; shaker 1, 13 Jackson
MGI ID:	MGI:5566827
Gene:	Myo7a  Location: Chr7:97700267-97768731 bp, - strand  Genetic Position: Chr7, 53.57 cM
Alliance:	Myo7ash1-13J page

Strain of Origin:

C.129S1(B6)-Gata1tm6Sho/J

Allele Type:    Spontaneous (Not Specified) Mutation:    Single point mutation   Mutation details: A spontaneous C to T transition at position 98,097,488 of chromosome 7 (GRCm38/mm10) changes amino acid 212 from arginine to histidine (p.R212H). (J:209272, 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 Myo7a Mutation:	118 strains or lines available

Original:	J:209272 Karst SY, et al., A new spontaneous mutation in myosin VIIa. MGI Direct Data Submission. 2014;
All:	2 reference(s)