cvd-logocvd - Molecule ID A1581

geneALB, GIG20, GIG42
nameSerum albumin precursor
speciesHomo sapiens

Molecule reference

SwissProtUniProtEnsEMBLGeneIDUniGeneOMIM
ALBU_HUMANP02768ENSG00000163631213Hs.418167103600, 194470

Functions and classifications

GOC:basement membrane, C:extracellular space, C:extracellular vesicular exosome, C:platelet alpha granule lumen, C:protein complex, F:antioxidant activity, F:copper ion binding, F:DNA binding, F:drug binding, F:fatty acid binding, F:pyridoxal phosphate binding, F:toxic substance binding, F:zinc ion binding, P:bile acid and bile salt transport, P:bile acid metabolic process, P:cellular response to starvation, P:hemolysis by symbiont of host erythrocytes, P:lipoprotein metabolic process, P:maintenance of mitochondrion location, P:negative regulation of apoptotic process, P:platelet activation, P:platelet degranulation, P:positive regulation of circadian sleep/wake cycle, non-REM sleep, P:response to mercury ion, P:response to nutrient, P:response to organic substance, P:response to platinum ion, P:sodium-independent organic anion transport, P:transmembrane transport, P:transport, F:cell surface binding, F:toxin binding, C:basement membrane, C:extracellular space, C:extracellular vesicular exosome, C:platelet alpha granule lumen, C:protein complex, F:antioxidant activity, F:copper ion binding, F:DNA binding, F:drug binding, F:fatty acid binding, F:pyridoxal phosphate binding, F:toxic substance binding, F:zinc ion binding, P:bile acid and bile salt transport, P:bile acid metabolic process, P:cellular response to starvation, P:hemolysis by symbiont of host erythrocytes, P:lipoprotein metabolic process, P:maintenance of mitochondrion location, P:negative regulation of apoptotic process, P:platelet activation, P:platelet degranulation, P:positive regulation of circadian sleep/wake cycle, non-REM sleep, P:response to mercury ion, P:response to nutrient, P:response to organic substance, P:response to platinum ion, P:sodium-independent organic anion transport, P:transmembrane transport, P:transport, F:cell surface binding, F:toxin binding
UniProt3D-structure, Alternative splicing, Cleavage on pair of basic residues, Complete proteome, Copper, Direct protein sequencing, Disease mutation, Disulfide bond, Glycation, Glycoprotein, Lipid-binding, Metal-binding, Phosphoprotein, Polymorphism, Reference proteome, Repeat, Secreted, Signal, Zinc
PADBTP: transport, storage, endocytosis, exocytosis, vesicles

Studies, tissues and diseases

Study IDSpeciesNTissue / SourceCompartmentDiseaseFold change in diseaseP-valueDetectionPubMed/DOI
Exp21417265Homo sapiens17heartmyocardiumDCM (Dilated cardiomyopathy)0.7000.007LC-MS/MS21417265
Exp22276806Homo sapiens16aortavalvesStenosis (Aortic stenosis)1.5610.007737MALDI-TOF/TOF22276806
Exp22276806Homo sapiens16aortavalvesStenosis (Aortic stenosis)1.6520.001892MALDI-TOF/TOF22276806
Exp22276806Homo sapiens16aortavalvesStenosis (Aortic stenosis)1.6650.01182MALDI-TOF/TOF22276806
Exp22276806Homo sapiens16aortavalvesStenosis (Aortic stenosis)1.6750.004436MALDI-TOF/TOF22276806
Exp22276806Homo sapiens16aortavalvesStenosis (Aortic stenosis)1.7600.005736MALDI-TOF/TOF22276806
Exp22276806Homo sapiens16aortavalvesStenosis (Aortic stenosis)1.7710.03754MALDI-TOF/TOF22276806
Exp22276806Homo sapiens16aortavalvesStenosis (Aortic stenosis)1.7940.005465MALDI-TOF/TOF22276806
Exp22276806Homo sapiens16aortavalvesStenosis (Aortic stenosis)1.8260.003753MALDI-TOF/TOF22276806
Exp22276806Homo sapiens16aortavalvesStenosis (Aortic stenosis)1.8660.004636MALDI-TOF/TOF22276806
Exp22276806Homo sapiens16aortavalvesStenosis (Aortic stenosis)1.9460.03196MALDI-TOF/TOF22276806
Exp25668619Homo sapiens10urinewholeCAD (Stable Coronary Artery Disease)0.284<0.05nanoLC-ESI-MS/MS25668619
Exp27350024bHomo sapiens40bloodplasmaCAD (Coronary artery disease (CAD) Verification Phase)0.9180.001ELISA27350024
Exp27350024cHomo sapiens506bloodplasmaCAD (Coronary artery disease (CAD) Validation Phase)0.880<0.0001ELISA27350024

Compile date 02-09-2018© C/VD project