cvd-logocvd - Molecule ID A4574

geneANXA13, ANX13
nameAnnexin A13
speciesHomo sapiens

Molecule reference

SwissProtUniProtEnsEMBLGeneIDUniGeneOMIM
ANX13_HUMANP27216ENSG00000104537312Hs.181107602573

Functions and classifications

GOC:endoplasmic reticulum lumen, C:extracellular space, C:Golgi lumen, C:plasma membrane, F:calcium ion binding, F:growth factor activity, F:serine-type endopeptidase activity, F:thrombospondin receptor activity, P:acute-phase response, P:blood coagulation, intrinsic pathway, P:cell surface receptor signaling pathway, P:cytosolic calcium ion homeostasis, P:fibrinolysis, P:leukocyte migration, P:negative regulation of astrocyte differentiation, P:negative regulation of fibrinolysis, P:negative regulation of platelet activation, P:negative regulation of proteolysis, P:peptidyl-glutamic acid carboxylation, P:platelet activation, P:positive regulation of cell growth, P:positive regulation of cell proliferation, P:positive regulation of collagen biosynthetic process, P:positive regulation of phosphatidylinositol 3-kinase signaling, P:positive regulation of phospholipase C-activating G-protein coupled receptor signaling pathway, P:positive regulation of protein phosphorylation, P:positive regulation of reactive oxygen species metabolic process, P:positive regulation of release of sequestered calcium ion into cytosol, P:post-translational protein modification, P:proteolysis, P:regulation of cell shape, P:regulation of gene expression, P:regulation of gene expression, C:extracellular region, P:blood coagulation, P:positive regulation of phosphatidylinositol 3-kinase cascade, P:regulation of cell shape
UniProtAlternative splicing, Annexin, Calcium, Calcium/phospholipid-binding, Cell membrane, Complete proteome, Lipoprotein, Membrane, Myristate, Polymorphism, Reference proteome, Repeat
PADBCS: Cell shape (cytoskeleton, cell adhesion, morphology, cell junction, cellular structures, extracellular matrix)

Studies, tissues and diseases

Study IDSpeciesNTissue / SourceCompartmentDiseaseP-valueDetectionPubMed/DOI
Exp26690514Homo sapiens24bloodwholeCAD (Coronary artery disease (CAD))1.28E-04Gene-array26690514

Compile date 02-09-2018© C/VD project