CKDdb-logoCKDdb - Molecule ID A389F

geneARTN, EVN
nameNeurotrophic factor artemin
speciesHomo sapiens

Molecule reference

SwissProtUniProtEnsEMBLGeneIDUniGeneOMIM
ARTN_HUMANQ5T4W7ENSG000001174079048Hs.632404603886

Functions and classifications

GOC:extracellular space, F:receptor binding, P:axon guidance, P:induction of positive chemotaxis, P:lymphocyte migration into lymphoid organs, P:neuroblast proliferation, P:peripheral nervous system development, P:Peyer's patch morphogenesis, P:signal transduction, C:extracellular region
UniProt3D-structure, Alternative splicing, Complete proteome, Disulfide bond, Glycoprotein, Growth factor, Polymorphism, Reference proteome, Secreted, Signal
PADBsignalling

Studies, tissues and diseases

Study IDSpeciesNTissue / SourceCompartmentDiseaseFold change in diseaseP-valueDetectionPubMed/DOI
Exp19698090bHomo sapiens25bloodmononuclear cellsDialysis (hemodialysis)0.410.00074RNA microarray19698090

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