Mus musculus Gene: Pgm2
Summary
InnateDB Gene IDBG-166725.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Pgm2
Gene Name phosphoglucomutase 2
Synonyms 2610020G18Rik; AA407108; AI098105; Pgm-2; Pgm1
Species Mus musculus
Ensembl Gene ENSMUSG00000025791
Encoded Proteins
phosphoglucomutase 2
phosphoglucomutase 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000079739:
The protein encoded by this gene is an isozyme of phosphoglucomutase (PGM) and belongs to the phosphohexose mutase family. There are several PGM isozymes, which are encoded by different genes and catalyze the transfer of phosphate between the 1 and 6 positions of glucose. In most cell types, this PGM isozyme is predominant, representing about 90% of total PGM activity. In red cells, PGM2 is a major isozyme. This gene is highly polymorphic. Mutations in this gene cause glycogen storage disease type 14. Alternativley spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Mar 2010]
The protein encoded by this gene is an isozyme of phosphoglucomutase (PGM) and belongs to the phosphohexose mutase family. There are several PGM isozymes, which are encoded by different genes and catalyze the transfer of phosphate between the 1 and 6 positions of glucose. In most cell types, this PGM isozyme is predominant, representing about 90%% of total PGM activity. In red cells, PGM2 is a major isozyme. This gene is highly polymorphic. Mutations in this gene cause glycogen storage disease type 14. Alternativley spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Mar 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 4:99929414-99987294
Strand Forward strand
Band C6
Transcripts
ENSMUST00000102783 ENSMUSP00000099844
ENSMUST00000058351 ENSMUSP00000061227
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
They are also associated with 22 interaction(s) predicted by orthology.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 22 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000287 magnesium ion binding
GO:0004614 phosphoglucomutase activity
GO:0016868 intramolecular transferase activity, phosphotransferases
Biological Process
GO:0005975 carbohydrate metabolic process
GO:0005978 glycogen biosynthetic process
GO:0006006 glucose metabolic process
GO:0019388 galactose catabolic process
Cellular Component
GO:0005829 cytosol
GO:0015629 actin cytoskeleton
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Disease pathway
Galactose catabolism pathway
Glucose metabolism pathway
Metabolism pathway
Glycogen synthesis pathway
Glycogen breakdown (glycogenolysis) pathway
Glycogen storage diseases pathway
Myoclonic epilepsy of Lafora pathway
Metabolism of carbohydrates pathway
KEGG
Pentose phosphate pathway pathway
Amino sugar and nucleotide sugar metabolism pathway
Glycolysis / Gluconeogenesis pathway
Starch and sucrose metabolism pathway
Galactose metabolism pathway
Purine metabolism pathway
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
TCR pathway
REACTOME
Glycogen breakdown (glycogenolysis) pathway
Galactose catabolism pathway
Myoclonic epilepsy of Lafora pathway
Glycogen synthesis pathway
Metabolism of carbohydrates pathway
Metabolism pathway
Disease pathway
Glucose metabolism pathway
Glycogen storage diseases pathway
Glycogen synthesis pathway
Metabolism of carbohydrates pathway
Myoclonic epilepsy of Lafora pathway
Glycogen storage diseases pathway
Glycogen breakdown (glycogenolysis) pathway
Glucose metabolism pathway
Metabolism pathway
Galactose catabolism pathway
Disease pathway
KEGG
Galactose metabolism pathway
Glycolysis / Gluconeogenesis pathway
Amino sugar and nucleotide sugar metabolism pathway
Pentose phosphate pathway pathway
Purine metabolism pathway
Starch and sucrose metabolism pathway
INOH
Glycolysis Gluconeogenesis pathway
Pentose phosphate cycle pathway
Galactose metabolism pathway
PID NCI
HIF-1-alpha transcription factor network
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Mm.412485
RefSeq NM_028132
OMIM
CCDS CCDS18388
HPRD
IMGT
MGI ID
MGI Symbol
EMBL
GenPept
RNA Seq Atlas