Mus musculus Gene: Pygm
Summary
InnateDB Gene IDBG-136275.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Pygm
Gene Name muscle glycogen phosphorylase
Synonyms AI115133; PG
Species Mus musculus
Ensembl Gene ENSMUSG00000032648
Encoded Proteins
muscle glycogen phosphorylase
muscle glycogen phosphorylase
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 ENSG00000068976:
This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Sep 2009]
Gene Information
Type Protein coding
Genomic Location Chromosome 19:6384399-6398459
Strand Forward strand
Band A
Transcripts
ENSMUST00000035269 ENSMUSP00000047564
ENSMUST00000113483 ENSMUSP00000109111
ENSMUST00000142755
ENSMUST00000139775
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 9 experimentally validated interaction(s) in this database.
They are also associated with 29 interaction(s) predicted by orthology.
Experimentally validated
Total 9 [view]
Protein-Protein 9 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 29 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000166 nucleotide binding
GO:0004645 phosphorylase activity
GO:0008184 glycogen phosphorylase activity
GO:0030170 pyridoxal phosphate binding
Biological Process
GO:0005975 carbohydrate metabolic process
GO:0005980 glycogen catabolic process
Cellular Component
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Disease pathway
Glucose metabolism pathway
Metabolism pathway
Glycogen breakdown (glycogenolysis) pathway
Glycogen storage diseases pathway
Myoclonic epilepsy of Lafora pathway
Metabolism of carbohydrates pathway
KEGG
Insulin signaling pathway pathway
Starch and sucrose metabolism pathway
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Glycogen breakdown (glycogenolysis) pathway
Myoclonic epilepsy of Lafora pathway
Metabolism of carbohydrates pathway
Metabolism pathway
Disease pathway
Glucose metabolism pathway
Glycogen storage diseases pathway
KEGG
Insulin signaling pathway pathway
Starch and sucrose metabolism pathway
INOH
PID NCI
Cross-References
SwissProt Q9WUB3
TrEMBL E9PUM3
UniProt Splice Variant
Entrez Gene 19309
UniGene Mm.27806
RefSeq NM_011224
OMIM
CCDS CCDS29504
HPRD
IMGT
MGI ID MGI:97830
MGI Symbol Pygm
EMBL AC167245 AF124787 BC012961
GenPept AAD30476 AAH12961
RNA Seq Atlas 19309