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SLC2A1 and STOM
Number of citations of the paper that reports this interaction (PMID
10562431
)
13
Data Source:
HPRD
(in vivo, in vitro)
SLC2A1
STOM
Gene Name
solute carrier family 2 (facilitated glucose transporter), member 1
stomatin
Image
No pdb structure
Gene Ontology Annotations
Cellular Component
Female Pronucleus
Cytosol
Plasma Membrane
Integral Component Of Plasma Membrane
Caveola
Cell-cell Junction
Membrane
Basolateral Plasma Membrane
Midbody
Cortical Actin Cytoskeleton
Melanosome
Extracellular Vesicular Exosome
Blood Microparticle
Extracellular Space
Cytoplasm
Cytoskeleton
Integral Component Of Plasma Membrane
Membrane
Vesicle
Melanosome
Membrane Raft
Extracellular Vesicular Exosome
Blood Microparticle
Molecular Function
Glucose Transmembrane Transporter Activity
Protein Binding
Kinase Binding
Dehydroascorbic Acid Transporter Activity
Identical Protein Binding
Xenobiotic Transporter Activity
Protein Self-association
D-glucose Transmembrane Transporter Activity
Protein Homodimerization Activity
Biological Process
Carbohydrate Metabolic Process
Energy Reserve Metabolic Process
Protein Complex Assembly
Vitamin Metabolic Process
Water-soluble Vitamin Metabolic Process
Response To Osmotic Stress
Hexose Transport
Pathogenesis
Glucose Transport
L-ascorbic Acid Metabolic Process
Cellular Response To Glucose Starvation
Xenobiotic Transport
Small Molecule Metabolic Process
Regulation Of Insulin Secretion
Transmembrane Transport
Dehydroascorbic Acid Transport
Protein Homooligomerization
Regulation Of Acid-sensing Ion Channel Activity
Pathways
Metabolism of vitamins and cofactors
Defective CD320 causes methylmalonic aciduria
Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF
Integration of energy metabolism
Defective BTD causes biotidinase deficiency
Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC
Defective MTR causes methylmalonic aciduria and homocystinuria type cblG
SLC-mediated transmembrane transport
Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE
Defective AMN causes hereditary megaloblastic anemia 1
Myoclonic epilepsy of Lafora
Glycogen storage diseases
Defects in cobalamin (B12) metabolism
Defective GIF causes intrinsic factor deficiency
Defective HLCS causes multiple carboxylase deficiency
Defective MMAB causes methylmalonic aciduria type cblB
Regulation of insulin secretion
Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD
Vitamin C (ascorbate) metabolism
Hexose transport
Defective MMAA causes methylmalonic aciduria type cblA
Defective CUBN causes hereditary megaloblastic anemia 1
Metabolism of water-soluble vitamins and cofactors
Defective MUT causes methylmalonic aciduria mut type
Defects in biotin (Btn) metabolism
Metabolism of carbohydrates
Glucose transport
Defective TCN2 causes hereditary megaloblastic anemia
Defects in vitamin and cofactor metabolism
Drugs
Diseases
GWAS
Cardiac hypertrophy (
21348951
)
Protein-Protein Interactions
11 interactors:
CALR
CANX
COPS6
GAPDH
GIPC1
PDIA3
PTK2B
STOM
SUMO1
UBE2I
VHL
9 interactors:
ASIC1
ASIC2
ASIC3
DVL3
LANCL1
RPL13A
RUVBL1
RUVBL2
SLC2A1
Entrez ID
6513
2040
HPRD ID
00683
00585
Ensembl ID
ENSG00000117394
ENSG00000148175
Uniprot IDs
P11166
Q59GX2
P27105
PDB IDs
1SUK
Enriched GO Terms of Interacting Partners
?
Post-translational Protein Modification
Peptidyl-amino Acid Modification
Regulation Of Protein Stability
Cellular Protein Modification Process
Posttranscriptional Regulation Of Gene Expression
Protein Stabilization
Cellular Protein Metabolic Process
Protein N-linked Glycosylation Via Asparagine
Protein N-linked Glycosylation
Antigen Processing And Presentation Of Peptide Antigen Via MHC Class I
Protein Localization To Nucleus
Protein Sumoylation
Response To Lithium Ion
Protein Metabolic Process
Antigen Processing And Presentation Of Peptide Antigen
Negative Regulation Of Cellular Metabolic Process
Immune System Process
Negative Regulation Of Gene Expression
Negative Regulation Of Biosynthetic Process
Regulation Of Translation
Protein Folding
Antigen Processing And Presentation
Regulation Of Intracellular Steroid Hormone Receptor Signaling Pathway
Chaperone-mediated Protein Folding
Protein Glycosylation
Macromolecule Glycosylation
Positive Regulation Of Leukocyte Chemotaxis
Glycosylation
Peptide Antigen Assembly With MHC Class I Protein Complex
Peptidyl-cysteine S-trans-nitrosylation
Positive Regulation Of SUMO Transferase Activity
Regulation Of Acid-sensing Ion Channel Activity
Endothelial Cell Migration
Regulation Of Protein Catabolic Process
Glycoprotein Biosynthetic Process
Regulation Of Signal Transduction
Positive Regulation Of Leukocyte Migration
Negative Regulation Of Translation
Epithelial Cell Migration
Epithelium Migration
Carbohydrate Metabolic Process
Regulation Of CGMP-mediated Signaling
Marginal Zone B Cell Differentiation
Positive Regulation Of B Cell Chemotaxis
Glycoprotein Metabolic Process
Protein Localization
Positive Regulation Of Chemotaxis
Negative Regulation Of Transcription, DNA-templated
Regulation Of Cellular Protein Metabolic Process
Antigen Processing And Presentation Of Exogenous Peptide Antigen Via MHC Class I, TAP-dependent
Sensory Perception Of Sour Taste
Response To PH
Sensory Perception Of Taste
Cellular Response To Stimulus
Histone H2A Acetylation
Cellular Response To PH
Response To Acidic PH
Response To Abiotic Stimulus
Sodium Ion Transmembrane Transport
Response To Stimulus
Detection Of Mechanical Stimulus Involved In Sensory Perception
Sodium Ion Transport
Detection Of Mechanical Stimulus
Histone H4 Acetylation
DNA Duplex Unwinding
DNA Geometric Change
Enterobactin Transport
Negative Regulation Of Formation Of Translation Preinitiation Complex
Regulation Of Systemic Arterial Blood Pressure By Aortic Arch Baroreceptor Feedback
Sensory Perception Of Chemical Stimulus
Detection Of Chemical Stimulus Involved In Sensory Perception Of Pain
Histone Acetylation
Internal Peptidyl-lysine Acetylation
Peptidyl-lysine Acetylation
Internal Protein Amino Acid Acetylation
Siderophore Transport
Negative Regulation Of Estrogen Receptor Binding
Transcriptional Activation By Promoter-enhancer Looping
Protein Acetylation
Dehydroascorbic Acid Transport
Monovalent Inorganic Cation Transport
Non-canonical Wnt Signaling Pathway Via JNK Cascade
Detection Of Abiotic Stimulus
Sensory Perception Of Mechanical Stimulus
Regulation Of Cellular Process
Chromatin Remodeling
Xenobiotic Transport
Non-canonical Wnt Signaling Pathway Via MAPK Cascade
Establishment Of Protein Localization To Chromatin
Regulation Of Systemic Arterial Blood Pressure By Baroreceptor Feedback
Transmembrane Transport
Sensory Perception
Ion Transport
Cellular Response To Acidic PH
Negative Regulation Of Receptor Binding
Response To Mechanical Stimulus
Metal Ion Transport
DNA Recombination
Peptidyl-lysine Modification
Cation Transmembrane Transport
Tagcloud
?
atp1a2
atp1b2
beef
corpus
cows
diestrus
follicle
glandular
gonadotropin
lcl
lf
luteum
manipulated
nelore
ovulation
p4
periovulatory
pof
preovulatory
proestrus
receptivity
slaughtered
slc37a4
washings
Tagcloud (Difference)
?
atp1a2
atp1b2
beef
corpus
cows
diestrus
follicle
glandular
gonadotropin
lcl
lf
luteum
manipulated
nelore
ovulation
p4
periovulatory
pof
preovulatory
proestrus
receptivity
slaughtered
slc37a4
washings
Tagcloud (Intersection)
?