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Golga1awag
Spontaneous Allele Detail
Nomenclature
Symbol: Golga1awag
Name: golgi autoantigen, golgin subfamily a, 1; ages with abnormal gait
MGI ID: MGI:3510600
Gene: Golga1  Location: Chr2:39016155-39065541 bp, - strand  Genetic Position: Chr2, 24.42 cM, cytoband B
Mutation
origin
Strain of Origin:  B6(Cg)-Tyrc-2J/J
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
 
Mutation detailsThis 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
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 anatomical structures
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:  5 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)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
04/06/2021
MGI 6.16
The Jackson Laboratory