cvd-logocvd - Molecule ID A823F

nameConserved hypothetical protein
speciesHomo sapiens

Molecule reference

SwissProtUniProtEnsEMBLGeneIDUniGeneOMIM
CI072_HUMANQ96LT7ENSG00000147894203228Hs.493639105550, 614260

Functions and classifications

GOC:cytosol, C:dendrite, C:membrane, C:neuronal cell body, C:plasma membrane, C:spliceosomal complex, F:GDP binding, F:GTP binding, F:GTPase activity, F:metal ion binding, P:cell cycle arrest, P:insulin receptor signaling pathway, P:positive regulation of TOR signaling, P:small GTPase mediated signal transduction, P:positive regulation of TOR signaling cascade
UniProtAlternative splicing, Amyotrophic lateral sclerosis, Complete proteome, Cytoplasm, Neurodegeneration, Nucleus, Polymorphism, Reference proteome
PADBDIS: disease

Studies, tissues and diseases

Study IDSpeciesNTissue / SourceCompartmentDiseaseFold change in diseaseP-valueDetectionPubMed/DOI
Exp19059264Homo sapiens31bloodmonocytes and T-helper cellsAtherosclerosis (Coronary Atherosclerosis)0.878<0.05Gene-array19059264
Exp21804111Mus musculus9aorta CAD (Coronary artery disease (CAD))1.268<0.05Gene-array21804111
Exp21868699aMus musculus20macrophages Atherosclerosis (Atherosclerosis)0.802<0.05Gene-array21868699
Exp21868699bMus musculus40aorta and macrophages CAD (Coronary artery disease (CAD))1.163<0.05Gene-array21868699
Exp24082102Mus musculus88heartwholeCAD (Coronary artery disease (CAD))1.273<0.05Gene-array24082102
Exp24530965Homo sapiens23bloodmononuclear cells (PBMCs)CAD (Familial Hypercholesterolemia and Coronary artery disease (CAD))0.804<0.05Gene-array24530965
Exp25835000Homo sapiens31macrophages CAD (Coronary artery disease (CAD))0.694<0.05Gene-array25835000
Exp26690514Homo sapiens24bloodwholeCAD (Coronary artery disease (CAD)) 1.49E-03Gene-array26690514
Exp27142736Mus musculus12liver CAD (Coronary artery disease (CAD))1.208<0.05Gene-array27142736

Compile date 02-09-2018© C/VD project