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

Symbol:	Golga1awag
Name:	golgin A1; ages with abnormal gait
MGI ID:	MGI:3510600
Gene:	Golga1  Location: Chr2:38906167-38955553 bp, - strand  Genetic Position: Chr2, 24.42 cM, cytoband B
Alliance:	Golga1awag page

Strain of Origin:

B6(Cg)-Tyrc-2J/J

Allele Type:    Spontaneous Mutation:    Intragenic deletion   Mutation details: This spontaneous mutation was discovered in 1998 at The Jackson Laboratory. The molecular lesion is a small intragenic deletion of TTCACAC at 39,023,425-431 (GRCm38) in the gene. This causes a frame shift and premature termination. (J:222308) Inheritance:    Recessive

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

In Structures Affected by this Mutation:

2 anatomical structure(s)

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 Golga1 Mutation:	34 strains or lines available

Original:	J:94744 Harris B, et al., A new mouse mutation with an abnormal gait as it ages is mapped to mouse Chromosome 2. MGI Direct Data Submission. 2004;
All:	2 reference(s)