solute carrier family 37 member 4

Summary
Gene Symbol
  • SLC37A4
Aliases
  • G6PT
  • GSD1b
  • GSD1c
  • GSD1d
  • Glucose-6-phosphate exchanger SLC37A4
  • SPX4
  • glucose-6-phosphatase transporter
  • sugar-phosphate exchange protein 4
Organism
Homo sapiens (human)
External Links
NCBI Gene
2542
HGNC
4061
KEGG Gene ID
hsa:2542
PubChem
2542
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Antiport
  • Congenital disorder of glycosylation
  • Disease variant
  • Endoplasmic reticulum
  • Glycogen storage disease
  • Reference proteome
  • Sugar transport
  • Transmembrane helix
Proteins
Displaying all 3 entries
UniProt Protein Name
O43826
  • Glucose-5-phosphate transporter
  • Glucose-6-phosphate translocase
  • Solute carrier family 37 member 4
  • Transformation-related gene 19 protein
B4DUH2
A8K0S7
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
Human Protein Atlas
ENSG00000137700

soft tissue soft tissue blood blood blood blood blood blood blood blood blood blood blood blood blood blood lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node kidney kidney adrenal gland adrenal gland breast breast duodenum stomach small intestine colon rectum appendix esophagus eye eye salivary gland nasopharynx nasopharynx tongue tonsil tonsil tonsil hair skin adipose tissue adipose tissue adipose tissue spinal cord oral mucosa lung lung heart bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus liver pancreas thyroid gland parathyroid gland parathyroid gland parathyroid gland parathyroid gland parathyroid gland spleen gallbladder ductus deferens ductus deferens seminal vesicle seminal vesicle seminal vesicle seminal vesicle testis testis epididymis epididymis brain smooth muscle urinary bladder prostate bone marrow skeletal muscle skeletal muscle skeletal muscle skeletal muscle skeletal muscle thymus thymus cartilage sole of foot sole of foot soft tissue blood blood blood blood blood blood blood blood blood blood blood blood lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lactating breast lactating breast kidney kidney adrenal gland adrenal gland duodenum stomach small intestine colon rectum appendix esophagus eye eye salivary gland salivary gland salivary gland salivary gland salivary gland salivary gland nasopharynx tongue tonsil tonsil hair skin adipose tissue adipose tissue adipose tissue adipose tissue adipose tissue adipose tissue adipose tissue spinal cord oral mucosa lung lung heart bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus liver pancreas thyroid gland parathyroid gland parathyroid gland parathyroid gland parathyroid gland parathyroid gland spleen gallbladder brain skeletal muscle skeletal muscle skeletal muscle skeletal muscle skeletal muscle thymus thymus smooth muscle urinary bladder vagina ovary ovary fallopian tube fallopian tube endometrium placenta cervix cervix bone marrow cartilage sole of foot sole of foot olfactory region cerebral cortex cerebellum medulla pons midbrain pituitary gland hypothalamus amygdala thalamus choroid plexus choroid plexus corpus callosum basal ganglia substantia nigra dorsal raphe dorsal raphe dorsal raphe dorsal raphe dorsal raphe dorsal raphe caudate hippocampus retina retina

Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.

KEGG BRITE Database
Orthology
K08171
Name
MFS transporter, OPA family, solute carrier family 37 (glycerol-6-phosphate transporter), member 4
References
Disease
Disease Ontology
Displaying entries 1 - 10 of 93 in total
DO ID Disease Name Source
DOID:0111043 glycogen storage disease IXc
DOID:0014667 disease of metabolism
DOID:0050571 congenital disorder of glycosylation type II
DOID:0050590 severe congenital neutropenia
DOID:0081330 glycogen storage disease Ib
DOID:0081331 glycogen storage disease Ic
DOID:0110741 type 1 diabetes mellitus 2
DOID:0110742 type 1 diabetes mellitus 3
DOID:0110743 type 1 diabetes mellitus 4
DOID:0110744 type 1 diabetes mellitus 5
The Human Phenotype Ontology
Displaying entries 41 - 50 of 135 in total
HPO ID HPO Term
HP:0000938 Osteopenia
HP:0000939 Osteoporosis
HP:0000978 Bruising susceptibility
HP:0000991 Xanthomatosis
HP:0001114 Xanthelasma
HP:0001252 Hypotonia
HP:0001263 Global developmental delay
HP:0001270 Motor delay
HP:0001397 Hepatic steatosis
HP:0001402 Hepatocellular carcinoma
Displaying all 4 entries
Disease ID Disease Name
OMIM:232240
  • glycogen storage disease Ib
OMIM:619525
  • congenital disorder of glycosylation, type IIw
ORPHA:79259
  • glycogen storage disease Ib
OMIM:232220
  • glycogen storage disease Ib

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Acknowledgements

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Last updated: August 19, 2024