Mus musculus Gene: Pgd
Summary
InnateDB Gene IDBG-204947.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Pgd
Gene Name phosphogluconate dehydrogenase
Synonyms 0610042A05Rik; AU019875; C78335
Species Mus musculus
Ensembl Gene ENSMUSG00000028961
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 4:149149991-149166771
Strand Reverse strand
Band E2
Transcripts
ENSMUST00000084124 ENSMUSP00000081141
ENSMUST00000124409
ENSMUST00000156120
ENSMUST00000137982
ENSMUST00000143944
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 14 interaction(s) predicted by orthology.
Predicted by orthology
Total 14 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004616 phosphogluconate dehydrogenase (decarboxylating) activity
GO:0050661 NADP binding
Biological Process
GO:0006098 pentose-phosphate shunt
GO:0009051 pentose-phosphate shunt, oxidative branch
GO:0019322 pentose biosynthetic process
GO:0019521 D-gluconate metabolic process
GO:0055114 oxidation-reduction process
Cellular Component
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
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
INOH
PID NCI
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
KEGG
Pentose phosphate pathway pathway
Glutathione metabolism pathway
INOH
Pentose phosphate cycle pathway
PID NCI
Cross-References
SwissProt Q9DCD0
TrEMBL
UniProt Splice Variant
Entrez Gene 110208
UniGene Mm.252080
RefSeq NM_001081274 XM_006535910 XM_006538472
OMIM
CCDS CCDS38974
HPRD
IMGT
MGI ID MGI:97553
MGI Symbol Pgd
EMBL AK002894 AK145602 AK150210 AK153409 AK155027 AK166733 AK166947 AK167215 AK168251
GenPept BAB22439 BAE26535 BAE29381 BAE31969 BAE32999 BAE38978 BAE39134 BAE39341 BAE40201
RNA Seq Atlas 110208