GPI - glucose-6-phosphate isomerase Gene

Also Known as AMF; NLK; PGI; PHI; GNPI; SA36; SA-36

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 2821

About GPI

Cytogenetic location: 19q13.11 Genomic coordinates (GRCh38): 19:34,359,718-34,402,413 (from NCBI)

This gene has 21 transcripts (splice variants), 1 gene allele, 278 orthologues and is associated with 2 phenotypes. Ubiquitous expression in heart (RPKM 54.9), fat (RPKM 52.6) and 25 other tissues.

Summary

This gene encodes a member of the glucose phosphate isomerase protein family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. In the cytoplasm, the gene product functions as a glycolytic enzyme (glucose-6-phosphate isomerase) that interconverts glucose-6-phosphate and fructose-6-phosphate. Extracellularly, the encoded protein (also referred to as neuroleukin) functions as a neurotrophic factor that promotes survival of skeletal motor neurons and sensory neurons, and as a lymphokine that induces immunoglobulin secretion. The encoded protein is also referred to as autocrine motility factor based on an additional function as a tumor-secreted cytokine and angiogenic factor. 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. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2016]

GPI Products (7)

mRNA Protein Name
NM_000175.5 NP_000166.2 glucose-6-phosphate isomerase isoform 2
NM_001184722.1 NP_001171651.1 glucose-6-phosphate isomerase isoform 1
NM_001289789.1 NP_001276718.1 glucose-6-phosphate isomerase isoform 3
NM_001289790.3 NP_001276719.1 glucose-6-phosphate isomerase isoform 4
NM_001329909.1 NP_001316838.1 glucose-6-phosphate isomerase isoform 2
NM_001329910.1 NP_001316839.1 glucose-6-phosphate isomerase isoform 2
NM_001329911.2 NP_001316840.1 glucose-6-phosphate isomerase isoform 5
Molecular Function GO Annotation Evidence Références Source
enables glucose-6-phosphate isomerase activity IDA
IDA: Inferred from direct assay
28803808 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
27499296 GOA
enables ubiquitin protein ligase binding IPI
IPI: Inferred from physical interaction
24810856 GOA
Biological Process GO Annotation Evidence Références Source
involved in glucose 6-phosphate metabolic process IDA
IDA: Inferred from direct assay
28803808 GOA
involved in positive regulation of endothelial cell migration IDA
IDA: Inferred from direct assay
1649192 GOA
involved in positive regulation of immunoglobulin production IDA
IDA: Inferred from direct assay
3020690 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

GPI Protein Structure

PGI

PGI: Phosphoglucose isomerase (54 - 546)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 558 a.a.
Protein Preferred Names Protein Names

glucose-6-phosphate isomerase

  • autocrine motility factor

Recombinant GPI Proteins

Cat. No. Nom du produit Accession Pureté
HY-P71680 Glucose-6-phosphate isomerase Protein, Human (His) P06744-1 (A2-E554) ≥ 95%, as determined by reducing SDS-PAGE.

GPI Anticorps

Cat. No. Nom du produit Application Reactivity
HY-P810641 Glucose 6 phosphate isomerase Antibody (YA9903) WB, IHC-P, FC, ICC/IF, IF-Tissue Human
HY-P82032 AMF Antibody (YA1777) WB, IHC-P, ICC/IF, FC Human
HY-P83978 Glucose-6-phosphate isomerase Antibody (YA3675) IHC-P, ICC/IF, ELISA Human
HY-P83978A Glucose-6-phosphate isomerase Antibody (YA3675)(PBS only) IHC-P, ICC/IF, ELISA Human
HY-P85191 AMF Antibody (YA4883) WB, IHC-P, ICC/IF, ELISA Human

Related Diseases

Diseases Alias
Hemolytic Anemia, Nonspherocytic, Due To Glucose Phosphate Isomerase Deficiency
  • Hemolytic Anemia Due To Glucophosphate Isomerase Deficiency

  • Hemolytic Anemia, Non-Spherocytic, Due To Glucose Phosphate Isomerase Deficiency

  • HA-GPID

  • Anemia, Hemolytic, Nonspherocytic, Due To Glucose Phosphate Isomerase Deficiency

Hemolytic Anemia
  • Anemia, Hemolytic

  • Anemia Hemolytic

  • Anaemia Due To Other Disorders Of Glutathione Metabolism

  • Chronic Non Spherocytic Anaemia

  • G6pd - [Glucose-6-Phosphate Dehydrogenase Deficiency] Anaemia

  • Anaemia Due To Glucose-6-Phosphate Dehydrogenase Deficiency

  • Glucose-6-Phosphate Dehydrogenase Deficiency With Anaemia

  • Glucose-6-Phosphate Dehydrogenase Deficiency Anaemia

  • Favism Anaemia

  • Haemolytic Anaemia Due Tog6pd Deficiency

  • Favism

  • Pentose Phosphate Pathway Disorder Anaemia

  • Anaemia Due To Pentose Phosphate Pathway Defect

Congenital Nonspherocytic Hemolytic Anemia
  • Hereditary Non-Spherocytic Hemolytic Anemia

  • Hereditary Nonspherocytic Hemolytic Anemia

  • Anemia, Hemolytic, Congenital Nonspherocytic

  • Congenital Nonspherocytic Hemolytic Anaemia

  • Hereditary Nonspherocytic Hemolytic Anaemia

  • Hnsha

Cutaneous Leishmaniasis
  • Diffuse Cutaneous Leishmaniasis

  • Asian Desert Cutaneous Leishmaniasis

  • Leishmaniasis, Cutaneous

  • Leproid Leishmaniasis

  • Leishmaniasis Diffuse Cutaneous

  • Leishmaniasis Cutaneous

  • Ethiopian Cutaneous Leishmaniasis

  • Old World Cutaneous Leishmaniasis

Congenital Hemolytic Anemia
  • Anemia Hemolytic Congenital

  • Anemia, Hemolytic, Congenital

  • Congenital Hemolytic Anaemia

  • Hereditary Hemolytic Anaemia

  • Hereditary Hemolytic Anemia

Transient Arthritis
Fibrosarcoma
  • Neoplasms, Fibrous Tissue

  • Fibrocytic Tumor

  • Fibrosarcoma Of Soft Tissue

  • Fibrous Tissue Neoplasm

Hyperoxaluria, Primary, Type Iii
  • Primary Hyperoxaluria Type 3

  • HP3

  • Ph Iii

  • Primary Hyperoxaluria Type Iii

  • Hyperoxaluria Primary 3

  • Hyperoxaluria Non-Hp1/Non-Hp2

  • Hyperoxaluria Non-Ph I/Ph Ii Form

  • Hyperoxaluria Primary Type Iii

Dermatitis, Atopic, 7
  • ATOD7

  • Dermatitis, Atopic, Susceptibility To, 7

  • Atopic Dermatitis 7

  • Dermatitis, Atopic 7

Arthritis
  • Inflammatory Joint Disease

  • Inflammatory Disorder Of Joint

Rheumatoid Arthritis
  • RA

  • Arthritis, Rheumatoid

  • Rheumatoid Arthritis, Susceptibility To

  • Arthritis Or Polyarthritis, Rheumatic

  • Atrophic Arthritis

  • Rheumatism Arthritis

  • Rheumatoid Polyarthritis

Pancreatic Cancer
  • Pancreatic Carcinoma

  • Carcinoma Of Pancreas

  • Familial Pancreatic Carcinoma

  • Pancreatic Neoplasm

  • Pancreatic Carcinoma, Familial

  • Malignant Neoplasm Of Pancreas

  • Pancreatic Acinar Carcinoma

  • Pancreatic Tumor

  • Familial Pancreatic Cancer

  • Neoplasm Of The Pancreas

  • Cancer Of The Pancreas

  • Pancreatic Carcinoma, Somatic

  • Pancreatic Cancer, Somatic

  • Ca Body Of Pancreas

  • Ca Head Of Pancreas

  • Ca Tail Of Pancreas

  • Malignant Neoplasm Of Body Of Pancreas

  • Malignant Neoplasm Of Head Of Pancreas

  • Malignant Neoplasm Of Tail Of Pancreas

  • Pancreas Neoplasm

  • Exocrine Cancer

  • Exocrine Pancreas Carcinoma

  • Hereditary Pancreatic Cancer

  • Hereditary Pancreatic Carcinoma

  • PNCA

  • Pancreatic Cancer, Susceptibility To

  • Carcinoma Of Head Of Pancreas

  • Pancreatic Neoplasms

  • Pancreatic Tumors

  • Cancer, Pancreatic

  • Cancer Of Pancreas

  • Mixed Islet Cell With Exocrine Carcinoma Of Unspecified Site

Alveolar Echinococcosis
  • Echinococcus Multilocularis Infection

  • Echinococcosis

  • Alveolococcosis

  • Multilocular Hydatid

  • Small Fox Tapeworm

Anemia, Congenital Dyserythropoietic, Type Ia
  • Congenital Dyserythropoietic Anemia Type I

  • Cda I

  • CDAN1A

  • Congenital Dyserythropoietic Anemia Type 1

  • Congenital Dyserythropoietic Anemia Type Ia

  • Congenital Dyserythropoietic Anemia, Type I

  • Anemia, Congenital Dyserythropoietic, Type I

  • Cda Type 1

  • Cda Type I

  • Cda Ia

  • Dyserythropoietic Anemia, Congenital Type 1

  • Anemia, Congenital Dyserythropoietic, Type 1a

  • Dyserythropoietic Anemia, Congenital, Type Ia

  • Cda, Type Ia

  • Congenital Dyserythropoietic Anaemia Type 1

  • Congenital Dyserythropoietic Anaemia Type I

  • Anemia, Dyserythropoietic, Congenital Type 1

  • Type I Congenital Dyserythropoietic Anemia

  • Anemia, Congenital Dyserythropoietic, 1a

  • Anemia, Dyserythropoietic, Congenital, Type Ia

Triosephosphate Isomerase Deficiency
  • TPID

  • Triose Phosphate-Isomerase Deficiency

  • Hemolytic Anemia Due To Triosephosphate Isomerase Deficiency

  • Tpi Deficiency

  • Triose Phosphate Isomerase Deficiency

  • Deficiency Of Phosphotriose Isomerase

  • Hereditary Nonspherocytic Hemolytic Anemia Due To Triosephosphate Isomerase Deficiency

Hereditary Spherocytosis
  • Congenital Spherocytic Hemolytic Anemia

  • Spherocytic Anemia

  • Congenital Spherocytosis

  • Spherocytosis, Type 1

  • Minkowski Chauffard Syndrome

  • Hs

  • Minkowski-Chauffard Disease

  • Minkowski-Chauffard Syndrome

  • Spherocytosis Hereditary

  • Spherocytosis, Hereditary

  • Anemia, Hereditary Spherocytic Hemolytic

Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema
  • Dehydrated Hereditary Stomatocytosis

  • Hereditary Xerocytosis

  • Xerocytosis, Hereditary

  • Pshk1

  • Pseudohyperkalemia Edinburgh

  • Dehydrated Hereditary Stomatocytosis With Or Without Pseudohyperkalemia And/Or Perinatal Edema

  • DHS1

  • Dhs

  • Hereditary Desiccytosis

  • Dehydrated Hereditary Stomatocytosis 1

  • Desiccytosis, Hereditary

  • Pseudohyperkalemia, Familial, 1, Due To Red Cell Leak

  • Pseudohyperkalemia Familial 1, Due To Red Cell Leak

  • Desiccytosis Hereditary

  • Xerocytosis Hereditary

  • Familial Pseudohyperkalemia 1 Due To Red Cell Leak

  • Stomatocytosis, Dehydrated, Hereditary, With/Without Pseudohyperkalemia And/Or Perinatal Edema

  • Xerocytosis

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris GPI VGNC VGNC:41381
Felis catus GPI VGNC VGNC:67409
Bos taurus GPI VGNC VGNC:29534
Rattus norvegicus GPI RGD RGD:2727
Mus musculus GPI MGD MGI:95797
Macaca fascicularis GPI NCBI NCBI:101865104
Macaca mulatta GPI NCBI NCBI:717980
Others GPI NCBI