Bos taurus Gene: PGD
Summary
InnateDB Gene IDBG-633131.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol PGD
Gene Name 6-phosphogluconate dehydrogenase, decarboxylating
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000013527
Encoded Proteins
phosphogluconate dehydrogenase
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 ENSG00000142657:
6-phosphogluconate dehydrogenase is the second dehydrogenase in the pentose phosphate shunt. Deficiency of this enzyme is generally asymptomatic, and the inheritance of this disorder is autosomal dominant. Hemolysis results from combined deficiency of 6-phosphogluconate dehydrogenase and 6-phosphogluconolactonase suggesting a synergism of the two enzymopathies. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 16:44043496-44058198
Strand Reverse strand
Band
Transcripts
ENSBTAT00000017988 ENSBTAP00000017988
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 12 interaction(s) predicted by orthology.
Predicted by orthology
Total 12 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004616 phosphogluconate dehydrogenase (decarboxylating) activity
GO:0016491 oxidoreductase activity
GO:0016616 oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0050661 NADP binding
GO:0050662 coenzyme binding
Biological Process
GO:0006098 pentose-phosphate shunt
GO:0009051 pentose-phosphate shunt, oxidative branch
GO:0019322 pentose biosynthetic process
GO:0055114 oxidation-reduction process
Cellular Component
GO:0005634 nucleus
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Pentose phosphate pathway (hexose monophosphate shunt) pathway
Myoclonic epilepsy of Lafora pathway
Metabolism of carbohydrates pathway
Metabolism pathway
Disease pathway
Glycogen storage diseases pathway
Disease pathway
Metabolism pathway
Pentose phosphate pathway (hexose monophosphate shunt) pathway
Glycogen storage diseases pathway
Myoclonic epilepsy of Lafora pathway
Metabolism of carbohydrates pathway
KEGG
Pentose phosphate pathway pathway
Glutathione metabolism pathway
Pentose phosphate pathway pathway
Glutathione metabolism pathway
INOH
Pentose phosphate cycle pathway
PID NCI
Cross-References
SwissProt
TrEMBL Q3ZCI4
UniProt Splice Variant
Entrez Gene 514939
UniGene Bt.13487
RefSeq NM_001143738
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL BC102178 DAAA02042990
GenPept AAI02179
RNA Seq Atlas 514939