Search Results for: ARL13B

134 interactions involving ARL13B - ADP ribosylation factor like GTPase 13B found:

Sort by: Symbol Number of Pathways Number of Drugs Number of Diseases
Novel Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
CD151 CD151 molecule (Raph blood group)
  • Assembly of collagen fibrils and other multimeric structures
  • Type I hemidesmosome assembly
  • Nephropathy with pretibial epidermolysis bullosa and deafness
CD302 CD302 molecule
CD53 CD53 molecule
  • Neutrophil degranulation
CDIPT CDP-diacylglycerol--inositol 3-phosphatidyltransferase
  • Synthesis of PI
  • scyllo-inositol
CFHR5 complement factor H related 5
  • Regulation of Complement cascade
CLDN4 claudin 4
  • Tight junction interactions
CLDN8 claudin 8
  • Tight junction interactions
CLEC4G C-type lectin domain family 4 member G
  • Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell
CLEC7A C-type lectin domain containing 7A
  • CLEC7A (Dectin-1) signaling
  • CLEC7A (Dectin-1) signaling
  • Chronic Mucocutaneous Candidiasis (CMC); Familial candidiasis (CANDF)
CLN6 CLN6 transmembrane ER protein
  • Neuronal ceroid lipofuscinosis, including: Infantile Neuronal Ceroid Lipofuscinosis (INCL)/ Santavuori-Haltia Disease (CLN1); Late-Infantile Neuronal Ceroid Lipofuscinosis (LINCL)/ Jansky-Bielschowsky Disease (CLN2); Juvenile Neuronal Ceroid Lipofuscinosis (JNCL)/Batten Disease/ Spielmeyer-Vogt Disease (CLN3); Adult Neuronal Ceroid Lipofuscinosis (ANCL)/ Kufs Disease (CLN4); LINCL variant (CLN5, CLN6, CLN7, CLN8); Batten Disease variant (CLN9); Congenital NCL (CLN10)
  • Progressive myoclonic epilepsy (PME), including: Lafora disease (LBD); Unverricht-Lundborg disease (ULD); Neuronal ceroid lipofuscinoses (NCL); Type I sialidosis; Action myoclonus-renal failure syndrome (AMRF); Type III Gaucher disease (GD)
CMTM3 CKLF like MARVEL transmembrane domain containing 3
CMTM7 CKLF like MARVEL transmembrane domain containing 7
COL8A2 collagen type VIII alpha 2 chain
  • Collagen degradation
  • Collagen degradation
  • Collagen biosynthesis and modifying enzymes
  • Assembly of collagen fibrils and other multimeric structures
  • Integrin cell surface interactions
  • Collagen chain trimerization
  • Posterior polymorphous corneal dystrophy (PPCD)
  • Fuchs corneal dystrophy (FECD); Fuchs endothelial corneal dystrophy
CSGALNACT2 chondroitin sulfate N-acetylgalactosaminyltransferase 2
  • Chondroitin sulfate biosynthesis
CTSA cathepsin A
  • Glycosphingolipid metabolism
  • MHC class II antigen presentation
  • Sialic acid metabolism
  • Defective NEU1 causes sialidosis
  • Neutrophil degranulation
  • Galactosialidosis
CXCL16 C-X-C motif chemokine ligand 16
  • Chemokine receptors bind chemokines
  • G alpha (i) signalling events
CYB561D2 cytochrome b561 family member D2
EBP EBP cholestenol delta-isomerase
  • Cholesterol biosynthesis via desmosterol
  • Cholesterol biosynthesis via lathosterol
  • Tamoxifen
EMP1 epithelial membrane protein 1
ENTPD3 ectonucleoside triphosphate diphosphohydrolase 3
  • Phosphate bond hydrolysis by NTPDase proteins

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