CKDdb-logoCKDdb - Molecule ID A4565

geneALMS1
nameAlstrom syndrome protein 1
speciesHomo sapiens

Molecule reference

SwissProtUniProtEnsEMBLGeneIDUniGeneOMIM
ALMS1_HUMANQ8TCU4ENSG000001161277840Hs.184720203800, 606844

Functions and classifications

GOC:centrosome, C:cilium, C:cytosol, C:microtubule basal body, C:spindle pole, P:endosomal transport, P:G2/M transition of mitotic cell cycle, P:regulation of stress fiber assembly, C:cytoplasm, P:apoptotic process, P:calcium-mediated signaling, P:cholesterol homeostasis, P:cilium assembly, P:developmental growth, P:epithelial cell proliferation, P:establishment of planar polarity, P:fat cell differentiation, P:glucose homeostasis, P:inner ear receptor stereocilium organization, P:negative regulation of multicellular organism growth, P:ovulation, P:regulation of fat cell differentiation, P:retinal rod cell development, P:sensory perception of sound, P:spermatid development, P:triglyceride metabolic process
UniProtAlternative splicing, Cell projection, Ciliopathy, Cilium, Complete proteome, Cone-rod dystrophy, Cytoplasm, Cytoskeleton, Deafness, Diabetes mellitus, Obesity, Phosphoprotein, Polymorphism, Reference proteome, Repeat
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)0.410.00209RNA microarray19698090
Exp21752957aHomo sapiens22kidneytubuliDiabetes (diabetic kidney disease)3.39< 0.05RNA microarray21752957

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