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Pgm2n
Spontaneous Allele Detail
Summary
Symbol: Pgm2n
Name: phosphoglucomutase 2; null variant
MGI ID: MGI:3758654
Synonyms: Pgm-1n
Gene: Pgm2  Location: Chr5:64250293-64285694 bp, + strand  Genetic Position: Chr5, 32.8 cM, cytoband C3.3
Alliance: Pgm2n page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Spontaneous (Null/knockout)
Mutation:    Undefined
 
Mutation detailsThis spontaneous mutation was identified by electropherogram analysis. In this mutation, the fastest migrating band (most anodal) of PGM isozymes is absent. The specific molecular lesion has not been identified.
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Pgm2 Mutation:  44 strains or lines available
Notes
Mice expressing this allele, either in the heterozygous or homozygous state, are viable, healthy, and fertile.
References
Original:  J:6623 Johnson FM, et al., A null mutation at the mouse Phosphoglucomutase-1 locus and a new locus Pgm-3. Biochem Genet. 1981 Jun;19(5-6):599-615
All:  1 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