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Gcgrem2Smoc
Endonuclease-mediated Allele Detail
Summary
Symbol: Gcgrem2Smoc
Name: glucagon receptor; endonuclease-mediated mutation 2, Shanghai Model Organisms Center
MGI ID: MGI:6690504
Synonyms: GcgrV369M
Gene: Gcgr  Location: Chr11:120421525-120429812 bp, + strand  Genetic Position: Chr11, 84.24 cM, cytoband E2
Alliance: Gcgrem2Smoc page
Mutation
origin
Strain of Origin:  C57BL/6JSmoc
Mutation
description
Allele Type:    Endonuclease-mediated (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsCRISPR/Cas9 technology generated a G to A change at position 1105 (c.1105G>A) resulting in a valine to methionine substitution at amino acid 369 (p.V369M). (J:300368)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 5 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 Gcgr Mutation:  8 strains or lines available
References
Original:  J:300368 Lin G, et al., Characterization of a naturally occurring mutation V368M in the human glucagon receptor and its association with metabolic disorders. Biochem J. 2020 Jul 17;477(13):2581-2594
All:  3 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
12/10/2024
MGI 6.24
The Jackson Laboratory