CKDdb-logoCKDdb - Molecule ID A852C

geneB9D1, MKSR1, B9
nameB9 domain-containing protein 1
speciesHomo sapiens

Molecule reference

SwissProtUniProtEnsEMBLGeneIDUniGeneOMIM
B9D1_HUMANQ9UPM9ENSG0000010864127077Hs.462445614144, 614209

Functions and classifications

GOC:centrosome, C:cytoplasm, C:membrane, C:microtubule basal body, C:TCTN-B9D complex, F:hedgehog receptor activity, P:camera-type eye development, P:cardiocyte differentiation, P:cilium assembly, P:embryonic digit morphogenesis, P:in utero embryonic development, P:neuroepithelial cell differentiation, P:regulation of protein localization, P:smoothened signaling pathway, C:cilium axoneme
UniProtAlternative splicing, Cell projection, Ciliopathy, Cilium biogenesis/degradation, Complete proteome, Cytoplasm, Cytoskeleton, Meckel syndrome, Polymorphism, Reference proteome
PADBCell shape (cytoskeleton, cell adhesion, morphology, cell junction, cellular structures, extracellular matrix)

Studies, tissues and diseases

Study IDSpeciesNTissue / SourceCompartmentDiseaseFold change in diseaseP-valueDetectionPubMed/DOI
Exp19698090bHomo sapiens25bloodmononuclear cellsDialysis (hemodialysis)0.260.00524RNA microarray19698090
Exp19698090bHomo sapiens25bloodmononuclear cellsDialysis (hemodialysis)0.310.000429RNA microarray19698090

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