Bos taurus Gene: BT.23217
Summary
InnateDB Gene IDBG-644025.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol BT.23217
Gene Name phosphoglycerate mutase 2
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000014547
Encoded Proteins
phosphoglycerate mutase 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 ENSG00000164708:
Phosphoglycerate mutase (PGAM) catalyzes the reversible reaction of 3-phosphoglycerate (3-PGA) to 2-phosphoglycerate (2-PGA) in the glycolytic pathway. The PGAM is a dimeric enzyme containing, in different tissues, different proportions of a slow-migrating muscle (MM) isozyme, a fast-migrating brain (BB) isozyme, and a hybrid form (MB). This gene encodes muscle-specific PGAM subunit. Mutations in this gene cause muscle phosphoglycerate mutase eficiency, also known as glycogen storage disease X. [provided by RefSeq, Sep 2009]
Gene Information
Type Protein coding
Genomic Location Chromosome 22:370972-373326
Strand Reverse strand
Band
Transcripts
ENSBTAT00000019336 ENSBTAP00000019336
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 2 interaction(s) predicted by orthology.
Predicted by orthology
Total 2 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003824 catalytic activity
GO:0004619 phosphoglycerate mutase activity
GO:0005515 protein binding
GO:0016853 isomerase activity
GO:0016868 intramolecular transferase activity, phosphotransferases
Biological Process
GO:0006096 glycolytic process
GO:0006941 striated muscle contraction
GO:0008152 metabolic process
Cellular Component
GO:0005634 nucleus
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Glycolysis pathway
Gluconeogenesis pathway
Myoclonic epilepsy of Lafora pathway
Metabolism of carbohydrates pathway
Metabolism pathway
Disease pathway
Glucose metabolism pathway
Glycogen storage diseases pathway
Disease pathway
Glycolysis pathway
Glucose metabolism pathway
Metabolism pathway
Gluconeogenesis pathway
Glycogen storage diseases pathway
Myoclonic epilepsy of Lafora pathway
Metabolism of carbohydrates pathway
KEGG
Glycolysis / Gluconeogenesis pathway
Glycine, serine and threonine metabolism pathway
Glycolysis / Gluconeogenesis pathway
Glycine, serine and threonine metabolism pathway
INOH
Glycolysis Gluconeogenesis pathway
PID NCI
Cross-References
SwissProt
TrEMBL F1N2F2
UniProt Splice Variant
Entrez Gene 515067
UniGene Bt.23217
RefSeq NM_001038111
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02053419
GenPept
RNA Seq Atlas 515067