cvd-logocvd - Molecule ID A018C

geneHBG1, PRO2979
nameHemoglobin subunit gamma 1Hemoglobin gamma-A and gamma-G chains
speciesHomo sapiens

Molecule reference

SwissProtUniProtEnsEMBLGeneIDUniGeneOMIM
HBG1_HUMANP69891ENSG000002139343047Hs.702189142200

Functions and classifications

GOC:cytosol, C:hemoglobin complex, F:heme binding, F:iron ion binding, F:oxygen binding, F:oxygen transporter activity, P:blood coagulation
UniProt3D-structure, Acetylation, Complete proteome, Direct protein sequencing, Disease mutation, Heme, Iron, Metal-binding, Oxygen transport, Polymorphism, Reference proteome, Transport
PADBTP: transport, storage, endocytosis, exocytosis, vesicles

Studies, tissues and diseases

Study IDSpeciesNTissue / SourceCompartmentDiseaseFold change in diseaseP-valueDetectionPubMed/DOI
Exp19059264Homo sapiens31bloodmonocytes and T-helper cellsAtherosclerosis (Coronary Atherosclerosis)1.210<0.05Gene-array19059264
Exp21804111Mus musculus9aorta CAD (Coronary artery disease (CAD))1.092<0.05Gene-array21804111
Exp21868699aMus musculus20macrophages Atherosclerosis (Atherosclerosis)3.294<0.05Gene-array21868699
Exp21868699bMus musculus40aorta and macrophages CAD (Coronary artery disease (CAD))3.294<0.05Gene-array21868699
Exp24082102Mus musculus88heartwholeCAD (Coronary artery disease (CAD))1.454<0.05Gene-array24082102
Exp24530965Homo sapiens23bloodmononuclear cells (PBMCs)CAD (Familial Hypercholesterolemia and Coronary artery disease (CAD))0.379<0.05Gene-array24530965
Exp25835000Homo sapiens31macrophages CAD (Coronary artery disease (CAD))1.456<0.05Gene-array25835000
Exp27142736Mus musculus12liver CAD (Coronary artery disease (CAD))0.592<0.05Gene-array27142736

Compile date 02-09-2018© C/VD project