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 21 - 30 of 93 in total
DO ID Disease Name Source
DOID:0110755 type 1 diabetes mellitus 18
DOID:0110756 type 1 diabetes mellitus 19
DOID:0110757 type 1 diabetes mellitus 20
DOID:0110758 type 1 diabetes mellitus 21
DOID:0110759 type 1 diabetes mellitus 22
DOID:0110760 type 1 diabetes mellitus 23
DOID:0110761 type 1 diabetes mellitus 24
DOID:0111040 glycogen storage disease IXd
DOID:0111041 glycogen storage disease IXb
DOID:0111042 glycogen storage disease IXa
The Human Phenotype Ontology
Displaying entries 1 - 10 of 135 in total
HPO ID HPO Term
HP:0000006 Autosomal dominant inheritance
HP:0000007 Autosomal recessive inheritance
HP:0000023 Inguinal hernia
HP:0000083 Renal insufficiency
HP:0000093 Proteinuria
HP:0000097 Focal segmental glomerulosclerosis
HP:0000105 Enlarged kidney
HP:0000121 Nephrocalcinosis
HP:0000132 Menorrhagia
HP:0000147 Polycystic ovaries
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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Last updated: August 19, 2024