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Golga2tm1.1Baos
Targeted Allele Detail
Summary
Symbol: Golga2tm1.1Baos
Name: golgin A2; targeted mutation 1.1, Shilai Bao
MGI ID: MGI:6358612
Synonyms: GM130fl, GM130flox
Gene: Golga2  Location: Chr2:32178299-32197925 bp, + strand  Genetic Position: Chr2, 22.09 cM
Alliance: Golga2tm1.1Baos page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:272184
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  129
Mutation
description
Allele Type:    Targeted (Conditional ready)
Mutation:    Insertion
 
Mutation detailsA loxP site was inserted upstream of exon 14 and an FRT flanked neo cassette and loxP site were inserted downstream of exon 14 via homologous recombination. Flp mediated recombination removed the neo cassette. (J:272184)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 3 anatomical structure(s)
Find Mice (IMSR)
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 Golga2 Mutation:  53 strains or lines available
References
Original:  J:272184 Liu C, et al., Loss of the golgin GM130 causes Golgi disruption, Purkinje neuron loss, and ataxia in mice. Proc Natl Acad Sci U S A. 2017 Jan 10;114(2):346-351
All:  4 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
04/16/2024
MGI 6.23
The Jackson Laboratory