Bos taurus Gene: BT.98113
Summary
InnateDB Gene IDBG-643970.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol BT.98113
Gene Name glycogen phosphorylase, muscle form
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000001032
Encoded Proteins
glycogen phosphorylase, muscle form
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 29:43606012-43617848
Strand Reverse strand
Band
Transcripts
ENSBTAT00000001373 ENSBTAP00000001373
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 31 interaction(s) predicted by orthology.
Predicted by orthology
Total 31 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004645 phosphorylase activity
GO:0008184 glycogen phosphorylase activity
GO:0016740 transferase activity
GO:0016757 transferase activity, transferring glycosyl groups
GO:0030170 pyridoxal phosphate binding
Biological Process
GO:0005975 carbohydrate metabolic process
GO:0005980 glycogen catabolic process
Cellular Component
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
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
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
Insulin signaling pathway pathway
Starch and sucrose metabolism pathway
INOH
PID NCI
Cross-References
SwissProt
TrEMBL F1MJ28
UniProt Splice Variant
Entrez Gene 327664
UniGene Bt.16003
RefSeq NM_175786
HUGO HGNC:9726
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02063538
GenPept
RNA Seq Atlas 327664