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Aliases for SLC2A1 Gene

Aliases for SLC2A1 Gene

  • Solute Carrier Family 2 Member 1 2 3
  • Solute Carrier Family 2 (Facilitated Glucose Transporter), Member 1 2 3 5
  • Choreoathetosis/Spasticity, Episodic (Paroxysmal Choreoathetosis/Spasticity) 2 3
  • Human T-Cell Leukemia Virus (I And II) Receptor 2 3
  • Glucose Transporter Type 1, Erythrocyte/Brain 3 4
  • HepG2 Glucose Transporter 3 4
  • GLUT-1 3 4
  • GLUT1 3 4
  • Receptor For HTLV-1 And HTLV-2 3
  • GLUT1DS 3
  • SDCHCN 3
  • DYT17 3
  • DYT18 3
  • EIG12 3
  • HTLVR 3
  • DYT9 3
  • GLUT 3
  • PED 3
  • CSE 3

External Ids for SLC2A1 Gene

Previous HGNC Symbols for SLC2A1 Gene

  • GLUT1
  • GLUT
  • HTLVR
  • CSE

Previous GeneCards Identifiers for SLC2A1 Gene

  • GC01P043382
  • GC01M042395
  • GC01M042855
  • GC01M042804
  • GC01M043060
  • GC01M043164
  • GC01M043391
  • GC01M041511

Summaries for SLC2A1 Gene

Entrez Gene Summary for SLC2A1 Gene

  • This gene encodes a major glucose transporter in the mammalian blood-brain barrier. The encoded protein is found primarily in the cell membrane and on the cell surface, where it can also function as a receptor for human T-cell leukemia virus (HTLV) I and II. Mutations in this gene have been found in a family with paroxysmal exertion-induced dyskinesia. [provided by RefSeq, Apr 2013]

GeneCards Summary for SLC2A1 Gene

SLC2A1 (Solute Carrier Family 2 Member 1) is a Protein Coding gene. Diseases associated with SLC2A1 include Glut1 Deficiency Syndrome 2 and Dystonia 9. Among its related pathways are Lactose synthesis and HTLV-I infection. GO annotations related to this gene include identical protein binding and transmembrane transporter activity. An important paralog of this gene is ENSG00000251357.

UniProtKB/Swiss-Prot for SLC2A1 Gene

  • Facilitative glucose transporter. This isoform may be responsible for constitutive or basal glucose uptake. Has a very broad substrate specificity; can transport a wide range of aldoses including both pentoses and hexoses.

Tocris Summary for SLC2A1 Gene

  • Glucose transporters enable the movement of glucose, a hydrophilic molecule, across the cell membrane. Glucose is an essential source of energy for mammalian cells, and is also used as a substrate in protein and lipid synthesis.

Gene Wiki entry for SLC2A1 Gene

No data available for PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for SLC2A1 Gene

Genomics for SLC2A1 Gene

Regulatory Elements for SLC2A1 Gene

Enhancers for SLC2A1 Gene
GeneHancer Identifier Score Enhancer Sources TSS distance (kb) Number of Genes Away Size (kb) Transcription Factor Binding Sites within enhancer Other Gene Targets for Enhancer

Enhancers around SLC2A1 on UCSC Golden Path with GeneCards custom track

Promoters for SLC2A1 Gene
Ensembl Regulatory Elements (ENSRs) TSS Distance (bp) Size (bp) Binding Sites for Transcription Factors within promoters

ENSRs around SLC2A1 on UCSC Golden Path with GeneCards custom track

Genomic Location for SLC2A1 Gene

Chromosome:
1
Start:
42,925,375 bp from pter
End:
42,959,176 bp from pter
Size:
33,802 bases
Orientation:
Minus strand

Genomic View for SLC2A1 Gene

Genes around SLC2A1 on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
SLC2A1 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for SLC2A1 Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for SLC2A1 Gene

Proteins for SLC2A1 Gene

  • Protein details for SLC2A1 Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    P11166-GTR1_HUMAN
    Recommended name:
    Solute carrier family 2, facilitated glucose transporter member 1
    Protein Accession:
    P11166
    Secondary Accessions:
    • A8K9S6
    • B2R620
    • D3DPX0
    • O75535
    • Q147X2

    Protein attributes for SLC2A1 Gene

    Size:
    492 amino acids
    Molecular mass:
    54084 Da
    Quaternary structure:
    • Interacts with GIPC (via PDZ domain) (By similarity). Found in a complex with ADD2, DMTN and SLC2A1. Interacts (via C-terminus cytoplasmic region) with DMTN isoform 2. Interacts with SNX27; the interaction is required when endocytosed to prevent degradation in lysosomes and promote recycling to the plasma membrane. Interacts with STOM.

    Three dimensional structures from OCA and Proteopedia for SLC2A1 Gene

neXtProt entry for SLC2A1 Gene

Proteomics data for SLC2A1 Gene at MOPED

Post-translational modifications for SLC2A1 Gene

  • Glycosylation at Asn 45
  • Modification sites at PhosphoSitePlus

Other Protein References for SLC2A1 Gene

Antibody Products

  • Cell Signaling Technology (CST) Antibodies for SLC2A1 (GLUT1)

No data available for DME Specific Peptides for SLC2A1 Gene

Domains & Families for SLC2A1 Gene

Gene Families for SLC2A1 Gene

Suggested Antigen Peptide Sequences for SLC2A1 Gene

Graphical View of Domain Structure for InterPro Entry

P11166

UniProtKB/Swiss-Prot:

GTR1_HUMAN :
  • Belongs to the major facilitator superfamily. Sugar transporter (TC 2.A.1.1) family. Glucose transporter subfamily.
Family:
  • Belongs to the major facilitator superfamily. Sugar transporter (TC 2.A.1.1) family. Glucose transporter subfamily.
genes like me logo Genes that share domains with SLC2A1: view

Function for SLC2A1 Gene

Molecular function for SLC2A1 Gene

GENATLAS Biochemistry:
solute carrier family 2,member A1,facilitated glucose transporter,not associated with susceptibility to NIDDM
UniProtKB/Swiss-Prot Function:
Facilitative glucose transporter. This isoform may be responsible for constitutive or basal glucose uptake. Has a very broad substrate specificity; can transport a wide range of aldoses including both pentoses and hexoses.

Gene Ontology (GO) - Molecular Function for SLC2A1 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0019900 kinase binding IEA --
GO:0042910 xenobiotic transporter activity IEA --
genes like me logo Genes that share ontologies with SLC2A1: view
genes like me logo Genes that share phenotypes with SLC2A1: view

Human Phenotype Ontology for SLC2A1 Gene

HPO Id HPO Name Alternative Ids Definition Synonyms

Animal Models for SLC2A1 Gene

MGI Knock Outs for SLC2A1:

Animal Model Products

  • Taconic Biosciences Mouse Models for SLC2A1

CRISPR Products

No data available for Enzyme Numbers (IUBMB) , Transcription Factor Targets and HOMER Transcription for SLC2A1 Gene

Localization for SLC2A1 Gene

Subcellular locations from UniProtKB/Swiss-Prot for SLC2A1 Gene

Cell membrane; Multi-pass membrane protein. Melanosome. Note=Localizes primarily at the cell surface. Identified by mass spectrometry in melanosome fractions from stage I to stage IV.

Subcellular locations from

COMPARTMENTS
Jensen Localization Image for SLC2A1 Gene COMPARTMENTS Subcellular localization image for SLC2A1 gene
Compartment Confidence
cytoskeleton 5
extracellular 5
plasma membrane 5
golgi apparatus 4
cytosol 3
nucleus 3
endoplasmic reticulum 2
mitochondrion 2
endosome 1
peroxisome 1
vacuole 1

Gene Ontology (GO) - Cellular Components for SLC2A1 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005829 cytosol IEA --
GO:0005901 caveola IEA --
GO:0016020 membrane IEA,TAS 3028891
GO:0016324 apical plasma membrane IEA --
GO:0030864 cortical actin cytoskeleton IDA 18347014
genes like me logo Genes that share ontologies with SLC2A1: view

Pathways & Interactions for SLC2A1 Gene

genes like me logo Genes that share pathways with SLC2A1: view

SIGNOR curated interactions for SLC2A1 Gene

Is activated by:

Gene Ontology (GO) - Biological Process for SLC2A1 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005989 lactose biosynthetic process TAS --
GO:0006112 energy reserve metabolic process TAS --
GO:0006767 water-soluble vitamin metabolic process TAS --
GO:0015758 glucose transport IEA,TAS --
genes like me logo Genes that share ontologies with SLC2A1: view

Drugs & Compounds for SLC2A1 Gene

(58) Drugs for SLC2A1 Gene - From: DrugBank, ApexBio, DGIdb, IUPHAR, Tocris, and Novoseek

Name Status Disease Links Group Role Mechanism of Action Clinical Trials
Etomidate Approved Pharma Carrier, inhibitor General anesthetic with GABA modulatory and GABA-mimetic actions 61
2-deoxyglucose Experimental, Investigational Pharma Transporter Non-metabolizable glucose analog; hexokinase substrate 0
dehydroascorbic acid Experimental Pharma Transporter 0
[<sup>3</sup>H]2-deoxyglucose Pharma 0
Metformin HCl Pharma Anti-diabetic drug 0

(55) Additional Compounds for SLC2A1 Gene - From: Novoseek, Tocris, and HMDB

Name Synonyms Role CAS Number PubChem IDs PubMed IDs
D-Glucose
  • Roferose ST
  • (+)-Glucose
  • Anhydrous dextrose
  • Cerelose
  • Cerelose 2001
50-99-7
D-(+)-Glucose
50-99-7
L-Dehydroascorbic acid
490-83-5
STF 31
724741-75-7

(4) Tocris Compounds for SLC2A1 Gene

Compound Action Cas Number
D-(+)-Glucose Naturally occurring monosaccharide 50-99-7
L-Dehydroascorbic acid GLUT1 substrate; anticancer 490-83-5
NVP DPP 728 dihydrochloride Potent, orally active dipeptidyl peptidase IV (DPP-IV) inhibitor 207556-62-5
STF 31 NAMPT inhibitor; also GLUT1 inhibitor 724741-75-7

(2) ApexBio Compounds for SLC2A1 Gene

Compound Action Cas Number
Metformin HCl Anti-diabetic drug 1115-70-4
Phloretin A dihydrochalcone found in apple 60-82-2
genes like me logo Genes that share compounds with SLC2A1: view

Transcripts for SLC2A1 Gene

Unigene Clusters for SLC2A1 Gene

Solute carrier family 2 (facilitated glucose transporter), member 1:
Representative Sequences:

CRISPR Products

Inhibitory RNA Products

Clone Products

Flow Cytometry Products

Alternative Splicing Database (ASD) splice patterns (SP) for SLC2A1 Gene

ExUns: 1a · 1b · 1c ^ 2 ^ 3a · 3b ^ 4a · 4b · 4c · 4d ^ 5a · 5b · 5c · 5d ^ 6 ^ 7 ^ 8a · 8b ^ 9 ^ 10 ^ 11a · 11b · 11c
SP1: - - - -
SP2: - -
SP3: - - -
SP4: - - -
SP5: - - - - - -
SP6: -
SP7: - - - - - - - - - -
SP8:

Relevant External Links for SLC2A1 Gene

GeneLoc Exon Structure for
SLC2A1
ECgene alternative splicing isoforms for
SLC2A1

Expression for SLC2A1 Gene

mRNA expression in normal human tissues for SLC2A1 Gene

mRNA expression in embryonic tissues and stem cells from LifeMap Discovery

mRNA differential expression in normal tissues according to GTEx for SLC2A1 Gene

This gene is overexpressed in Nerve - Tibial (x6.2) and Skin - Not Sun Exposed (Suprapubic) (x4.3).

Protein differential expression in normal tissues from HIPED for SLC2A1 Gene

This gene is overexpressed in Nasal epithelium (27.8), Retina (15.7), and Placenta (10.9).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB, PaxDb, and MOPED for SLC2A1 Gene



SOURCE GeneReport for Unigene cluster for SLC2A1 Gene Hs.473721

mRNA Expression by UniProt/SwissProt for SLC2A1 Gene

P11166-GTR1_HUMAN
Tissue specificity: Detected in erythrocytes (at protein level). Expressed at variable levels in many human tissues.
genes like me logo Genes that share expression patterns with SLC2A1: view

Primer Products

No data available for Protein tissue co-expression partners for SLC2A1 Gene

Orthologs for SLC2A1 Gene

This gene was present in the common ancestor of animals and fungi.

Orthologs for SLC2A1 Gene

Organism Taxonomy Gene Similarity Type Details
cow
(Bos Taurus)
Mammalia SLC2A1 35
  • 92.34 (n)
  • 97.15 (a)
SLC2A1 36
  • 97 (a)
OneToOne
dog
(Canis familiaris)
Mammalia SLC2A1 35
  • 93.29 (n)
  • 97.36 (a)
SLC2A1 36
  • 94 (a)
OneToOne
mouse
(Mus musculus)
Mammalia Slc2a1 35
  • 89.5 (n)
  • 97.15 (a)
Slc2a1 16
Slc2a1 36
  • 97 (a)
OneToOne
chimpanzee
(Pan troglodytes)
Mammalia SLC2A1 35
  • 98.88 (n)
  • 98.31 (a)
SLC2A1 36
  • 95 (a)
OneToOne
rat
(Rattus norvegicus)
Mammalia Slc2a1 35
  • 89.63 (n)
  • 97.76 (a)
oppossum
(Monodelphis domestica)
Mammalia SLC2A1 36
  • 89 (a)
OneToOne
platypus
(Ornithorhynchus anatinus)
Mammalia SLC2A1 36
  • 86 (a)
OneToOne
chicken
(Gallus gallus)
Aves SLC2A1 35
  • 80.87 (n)
  • 88.52 (a)
SLC2A1 36
  • 89 (a)
OneToOne
African clawed frog
(Xenopus laevis)
Amphibia MGC53301 35
zebrafish
(Danio rerio)
Actinopterygii slc2a1b 35
  • 72.51 (n)
  • 80 (a)
slc2a1a 36
  • 75 (a)
OneToMany
slc2a1b 36
  • 79 (a)
OneToMany
rainbow trout
(Oncorhynchus mykiss)
Actinopterygii Omy.11901 35
fruit fly
(Drosophila melanogaster)
Insecta CG7882 37
  • 34 (a)
Glut1 37
  • 50 (a)
sut1 37
  • 37 (a)
sut2 37
  • 30 (a)
sut3 37
  • 30 (a)
sut4 37
  • 33 (a)
Glut1 36
  • 30 (a)
OneToMany
worm
(Caenorhabditis elegans)
Secernentea C35A11.4 37
  • 26 (a)
F48E3.2 37
  • 23 (a)
F53H8.3 37
  • 32 (a)
H17B01.1a 37
  • 39 (a)
H17B01.1b 37
  • 39 (a)
K08F9.1 37
  • 27 (a)
R09B5.11 37
  • 37 (a)
Y37A1A.3 37
  • 25 (a)
Y61A9LA.1 37
  • 22 (a)
F53H8.3 36
  • 27 (a)
ManyToMany
fgt-1 36
  • 37 (a)
ManyToMany
R09B5.11 36
  • 35 (a)
ManyToMany
A. gosspyii yeast
(Ashbya gossypii)
Saccharomycetes AGOS_AFL034W 35
  • 47.98 (n)
  • 33.33 (a)
baker's yeast
(Saccharomyces cerevisiae)
Saccharomycetes -- 36
  • 28 (a)
ManyToMany
VPS73 36
  • 26 (a)
ManyToMany
sea squirt
(Ciona intestinalis)
Ascidiacea Cin.7007 35
sea squirt
(Ciona savignyi)
Ascidiacea CSA.7972 36
  • 47 (a)
OneToMany
Species with no ortholog for SLC2A1:
  • Actinobacteria (Mycobacterium tuberculosis)
  • African malaria mosquito (Anopheles gambiae)
  • Alicante grape (Vitis vinifera)
  • alpha proteobacteria (Wolbachia pipientis)
  • amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • barley (Hordeum vulgare)
  • beta proteobacteria (Neisseria meningitidis)
  • bread mold (Neurospora crassa)
  • Chromalveolata (Phytophthora infestans)
  • common water flea (Daphnia pulex)
  • corn (Zea mays)
  • E. coli (Escherichia coli)
  • filamentous fungi (Aspergillus nidulans)
  • Firmicute bacteria (Streptococcus pneumoniae)
  • fission yeast (Schizosaccharomyces pombe)
  • green algae (Chlamydomonas reinhardtii)
  • honey bee (Apis mellifera)
  • K. lactis yeast (Kluyveromyces lactis)
  • lizard (Anolis carolinensis)
  • loblloly pine (Pinus taeda)
  • malaria parasite (Plasmodium falciparum)
  • medicago trunc (Medicago Truncatula)
  • moss (Physcomitrella patens)
  • orangutan (Pongo pygmaeus)
  • pig (Sus scrofa)
  • rice (Oryza sativa)
  • rice blast fungus (Magnaporthe grisea)
  • schistosome parasite (Schistosoma mansoni)
  • sea anemone (Nematostella vectensis)
  • sea urchin (Strongylocentrotus purpuratus)
  • sorghum (Sorghum bicolor)
  • soybean (Glycine max)
  • stem rust fungus (Puccinia graminis)
  • sugarcane (Saccharum officinarum)
  • thale cress (Arabidopsis thaliana)
  • tomato (Lycopersicon esculentum)
  • toxoplasmosis (Toxoplasma gondii)
  • Trichoplax (Trichoplax adhaerens)
  • tropical clawed frog (Silurana tropicalis)
  • wheat (Triticum aestivum)

Evolution for SLC2A1 Gene

ENSEMBL:
Gene Tree for SLC2A1 (if available)
TreeFam:
Gene Tree for SLC2A1 (if available)

Paralogs for SLC2A1 Gene

Pseudogenes.org Pseudogenes for SLC2A1 Gene

genes like me logo Genes that share paralogs with SLC2A1: view

Variants for SLC2A1 Gene

Sequence variations from dbSNP and Humsavar for SLC2A1 Gene

SNP ID Clin Chr 01 pos Sequence Context AA Info Type
VAR_013182 GLUT1 deficiency syndrome 1 (GLUT1DS1)
VAR_013183 GLUT1 deficiency syndrome 1 (GLUT1DS1)
VAR_013184 GLUT1 deficiency syndrome 1 (GLUT1DS1)
VAR_013185 GLUT1 deficiency syndrome 1 (GLUT1DS1)
VAR_013283 GLUT1 deficiency syndrome 1 (GLUT1DS1)

Structural Variations from Database of Genomic Variants (DGV) for SLC2A1 Gene

Variant ID Type Subtype PubMed ID
nsv699 CNV Insertion 18451855
esv2657422 CNV Deletion 23128226

Variation tolerance for SLC2A1 Gene

Residual Variation Intolerance Score: 10.4% of all genes are more intolerant (likely to be disease-causing)
Gene Damage Index Score: 0.56; 12.10% of all genes are more intolerant (likely to be disease-causing)

Relevant External Links for SLC2A1 Gene

Human Gene Mutation Database (HGMD)
SLC2A1

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot for SLC2A1 Gene

Disorders for SLC2A1 Gene

MalaCards: The human disease database

(68) MalaCards diseases for SLC2A1 Gene - From: OMIM, ClinVar, GeneTests, Orphanet, Swiss-Prot, DISEASES, Novoseek, and GeneCards

Disorder Aliases PubMed IDs
glut1 deficiency syndrome 2
  • dystonia 18
dystonia 9
  • choreoathetosis/spasticity, episodic
epilepsy, idiopathic generalized, suscpetibility to, 12
  • epilepsy, idiopathic generalized 12
glut1 deficiency syndrome 1
  • glut-1 deficiency syndrome
paroxysmal dystonic choreathetosis with episodic ataxia and spasticity
  • choreoathetosis/spasticity, episodic
- elite association - COSMIC cancer census association via MalaCards

UniProtKB/Swiss-Prot

GTR1_HUMAN
  • Dystonia 9 (DYT9) [MIM:601042]: An autosomal dominant neurologic disorder characterized by childhood onset of paroxysmal choreoathetosis and progressive spastic paraplegia. Most patients show some degree of cognitive impairment. Other variable features may include seizures, migraine headaches, and ataxia. {ECO:0000269 PubMed:21832227}. Note=The disease is caused by mutations affecting the gene represented in this entry.
  • Epilepsy, idiopathic generalized 12 (EIG12) [MIM:614847]: A disorder characterized by recurring generalized seizures in the absence of detectable brain lesions and/or metabolic abnormalities. Generalized seizures arise diffusely and simultaneously from both hemispheres of the brain. Seizure types include juvenile myoclonic seizures, absence seizures, and generalized tonic-clonic seizures. In some EIG12 patients seizures may remit with age. {ECO:0000269 PubMed:19798636, ECO:0000269 PubMed:22282645}. Note=The disease is caused by mutations affecting the gene represented in this entry.
  • GLUT1 deficiency syndrome 1 (GLUT1DS1) [MIM:606777]: A neurologic disorder showing wide phenotypic variability. The most severe classic phenotype comprises infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, motor incoordination, and spasticity. Onset of seizures, usually characterized by apneic episodes, staring spells, and episodic eye movements, occurs within the first 4 months of life. Other paroxysmal findings include intermittent ataxia, confusion, lethargy, sleep disturbance, and headache. Varying degrees of cognitive impairment can occur, ranging from learning disabilities to severe mental retardation. {ECO:0000269 PubMed:10227690, ECO:0000269 PubMed:10980529, ECO:0000269 PubMed:11136715, ECO:0000269 PubMed:11603379, ECO:0000269 PubMed:12325075, ECO:0000269 PubMed:15622525, ECO:0000269 PubMed:19901175, ECO:0000269 PubMed:20129935, ECO:0000269 PubMed:20221955, ECO:0000269 PubMed:20574033}. Note=The disease is caused by mutations affecting the gene represented in this entry.
  • GLUT1 deficiency syndrome 2 (GLUT1DS2) [MIM:612126]: A clinically variable disorder characterized primarily by onset in childhood of paroxysmal exercise-induced dyskinesia. The dyskinesia involves transient abnormal involuntary movements, such as dystonia and choreoathetosis, induced by exercise or exertion, and affecting the exercised limbs. Some patients may also have epilepsy, most commonly childhood absence epilepsy. Mild mental retardation may also occur. In some patients involuntary exertion-induced dystonic, choreoathetotic, and ballistic movements may be associated with macrocytic hemolytic anemia. {ECO:0000269 PubMed:14605501, ECO:0000269 PubMed:18451999, ECO:0000269 PubMed:19630075, ECO:0000269 PubMed:19798636, ECO:0000269 PubMed:20129935, ECO:0000269 PubMed:20574033, ECO:0000269 PubMed:20621801, ECO:0000269 PubMed:20830593, ECO:0000269 PubMed:21204808}. Note=The disease is caused by mutations affecting the gene represented in this entry.

Genatlas disease for SLC2A1 Gene

infantile seizures,microcephaly,developmental delay and hypoglycorrhachia,caused by haploinsufficiency of the blood-brain barrier hexose carrier

Relevant External Links for SLC2A1

Genetic Association Database (GAD)
SLC2A1
Human Genome Epidemiology (HuGE) Navigator
SLC2A1
Atlas of Genetics and Cytogenetics in Oncology and Haematology:
SLC2A1
genes like me logo Genes that share disorders with SLC2A1: view

Publications for SLC2A1 Gene

  1. Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect. (PMID: 21832227) Weber Y.G. … Lerche H. (Neurology 2011) 2 3 4 67
  2. The ubiquitous glucose transporter GLUT-1 is a receptor for HTLV. (PMID: 14622599) Manel N. … Battini J.L. (Cell 2003) 2 3 23
  3. Overexpression of GLUT-1 in the invasion front is associated with depth of oral squamous cell carcinoma and prognosis. (PMID: 19709351) Ohba S. … Hino O. (J. Oral Pathol. Med. 2010) 3 23
  4. Diabetes and obesity during pregnancy alter insulin signalling and glucose transporter expression in maternal skeletal muscle and subcutaneous adipose tissue. (PMID: 19955252) Colomiere M. … Lappas M. (J. Mol. Endocrinol. 2010) 3 23
  5. Resistin modulates glucose uptake and glucose transporter-1 (GLUT-1) expression in trophoblast cells. (PMID: 18410529) Di Simone N. … Caruso A. (J. Cell. Mol. Med. 2009) 3 23

Products for SLC2A1 Gene

Sources for SLC2A1 Gene

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