Gene: GPI (glucose-6-phosphate isomerase)  Homo sapiens

Symbol: GPI
Name: glucose-6-phosphate isomerase
Description: This gene belongs to the GPI family whose members encode multifunctional phosphoglucose isomerase proteins involved in energy pathways. The protein encoded by this gene is a dimeric enzyme that catalyzes the reversible isomerization of glucose-6-phosphate and fructose-6-phosphate. The protein functions in different capacities inside and outside the cell. In the cytoplasm, the gene product is involved in glycolysis and gluconeogenesis, while outside the cell it functions as a neurotrophic factor for spinal and sensory neurons. Defects in this gene are the cause of nonspherocytic hemolytic anemia and a severe enzyme deficiency can be associated with hydrops fetalis, immediate neonatal death and neurological impairment. [provided by RefSeq, Jul 2008]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: AMF; autocrine motility factor; DKFZp686C13233; glucose phosphate isomerase; glucose-6-phosphate isomerase; GNPI; hexose monophosphate isomerase; hexosephosphate isomerase; neuroleukin; NLK; oxoisomerase; PGI; PHI; phosphoglucose isomerase; phosphohexomutase; phosphohexose isomerase; phosphosaccharomutase; SA-36; SA36; sperm antigen 36; sperm antigen-36
Orthologs: Mus musculus : Gpi1 (glucose phosphate isomerase 1)  MGI
Rattus norvegicus : Gpi (glucose-6-phosphate isomerase)
Latest Assembly: Human Genome Assembly GRCh37
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_11935,013,732 - 35,051,389+NCBI
Human Genome Assembly HuRef1931,360,777 - 31,377,222+NCBI
Human Genome Assembly HuRef1931,390,807 - 31,399,974+NCBI
Human Genome Assembly GRCh371934,855,645 - 34,893,318+NCBI
Human Genome Assembly Build 361939,547,909 - 39,583,076+NCBI
Human Cytogenetic Map19q13.1 NCBI
Human Genome Assembly1939,547,908 - 39,583,076 NCBI
Model

Launch Genome Browser (GBrowse) : build 36 (hg18) build 37 (hg19)


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Molecular Pathway Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Human Genome Assembly GRCh37)

Sequence

Nucleotide Sequences
Protein Sequences
Promoters

Additional Information

External Database Links
Nomenclature History
 
More on GPI
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 1344852
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2013-04-23
Status: ACTIVE