cvd-logocvd - Molecule ID A774B

geneABCA13
nameABC A13
speciesHomo sapiens

Molecule reference

SwissProtUniProtEnsEMBLGeneIDUniGeneOMIM
ABCAD_HUMANQ86UQ4ENSG00000179869154664Hs.226568607807

Functions and classifications

GOC:cell surface, C:endoplasmic reticulum, C:extracellular space, C:Golgi stack, C:plasma membrane, F:arylsulfatase activity, F:calcium ion binding, F:N-acetylglucosamine-6-sulfatase activity, P:bone development, P:chondrocyte development, P:embryonic skeletal system development, P:esophagus smooth muscle contraction, P:glial cell-derived neurotrophic factor receptor signaling pathway, P:glomerular basement membrane development, P:glomerular filtration, P:heparan sulfate proteoglycan metabolic process, P:innervation, P:negative regulation of fibroblast growth factor receptor signaling pathway, P:positive regulation of Wnt signaling pathway, P:positive regulation vascular endothelial growth factor production, C:Golgi apparatus, F:sulfuric ester hydrolase activity, F:catalytic activity, P:positive regulation of Wnt receptor signaling pathway
UniProtAlternative splicing, ATP-binding, Complete proteome, Membrane, Nucleotide-binding, Polymorphism, Reference proteome, Repeat, Transmembrane, Transmembrane helix, Transport
PADBTP: transport, storage, endocytosis, exocytosis, vesicles

Studies, tissues and diseases

Study IDSpeciesNTissue / SourceCompartmentDiseaseP-valueDetectionPubMed/DOI
Exp26690514Homo sapiens24bloodwholeCAD (Coronary artery disease (CAD))4.59E-02Gene-array26690514

Compile date 02-09-2018© C/VD project