Golga1^awag
Spontaneous Allele Detail

Summary

• Symbol: Golga1^awag
• 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: Golga1^awag page

Mutation origin

• Strain of Origin: B6(Cg)-Tyr^c-2J/J

Mutation description

• 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

Expression

In Structures Affected by this Mutation:

2 anatomical structure(s)

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 Golga1 Mutation: 34 strains or lines available

References

• 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)