CKDdb-logoCKDdb - Molecule ID A4433

nameCalcium channel
speciesHomo sapiens

Molecule reference

CACB4_HUMANO00305ENSG00000182389785Hs.120725601949, 607682, 613855, 606904, 600669

Functions and classifications

GOC:cytoplasmic side of plasma membrane, C:cytosol, C:plasma membrane, C:synapse, C:voltage-gated calcium channel complex, F:voltage-gated calcium channel activity, P:adult walking behavior, P:axon guidance, P:calcium ion transmembrane transport, P:cAMP metabolic process, P:cellular calcium ion homeostasis, P:detection of light stimulus involved in visual perception, P:gamma-aminobutyric acid secretion, P:gamma-aminobutyric acid signaling pathway, P:membrane depolarization, P:muscle fiber development, P:neuromuscular junction development, P:neuronal action potential propagation, P:Peyer's patch development, P:regulation of ion transmembrane transport, P:regulation of voltage-gated calcium channel activity, P:spleen development, P:synaptic transmission, P:synaptic transmission, glutamatergic, P:T cell receptor signaling pathway, P:thymus development, P:transport, C:voltage-gated calcium channel complex, P:regulation of membrane potential, P:thymus development, C:cytosol, C:internal side of plasma membrane
UniProt3D-structure, Alternative splicing, Calcium, Calcium channel, Calcium transport, Complete proteome, Disease mutation, Epilepsy, Ion channel, Ion transport, Phosphoprotein, Reference proteome, SH3 domain, Transport, Voltage-gated channel

Studies, tissues and diseases

Study IDSpeciesNTissue / SourceCompartmentDiseaseFold change in diseaseP-valueDetectionPubMed/DOI
Exp19698090bHomo sapiens25bloodmononuclear cellsDialysis (hemodialysis)0.270.000000623RNA microarray19698090

Compile date 08-10-2018© iMODE-CKD consortium