Pgm2^m3H
Chemically induced Allele Detail

Summary

• Symbol: Pgm2^m3H
• Name: phosphoglucomutase 2; mutation 3, Harwell
• MGI ID: MGI:5305329
• Gene: Pgm2 Location: Chr5:64250293-64285694 bp, + strand Genetic Position: Chr5, 32.8 cM, cytoband C3.3
• Alliance: Pgm2^m3H page

Mutation origin

• Strain of Origin: 101/H

Mutation description

• Allele Type: Chemically induced (ENU)
• Mutation: Undefined
• Electrophoretic gel analysis confirmed the expression of an electrophoretic mobility variant. (J:180050)

Phenotypes

Key:

hm	homozygous	ht	heterozygous	tg	involves transgenes	√	phenotype observed
cn	conditional genotype	cx	complex: > 1 genome feature	ot	other: hemizygous, indeterminate,...	N	normal phenotype

Genotype/
Background:

	Allelic Composition	Genetic Background	Cell Line(s)
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hm1	Pgm2^m3H/Pgm2^m3H	involves: 101/H

Phenotypes:

Affected Systems	hm1
show or hide all annotated terms
normal phenotype	√
no abnormal phenotype detected	√

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: 46 strains or lines available

References

• Original: J:180050 Harwell MRC, Direct Data Submission 2012/02/09. MGI Direct Data Submission. 2012
• All: 2 reference(s)