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
Novel ARL6 ADP ribosylation factor like GTPase 6
  • BBSome-mediated cargo-targeting to cilium
  • Bardet-Biedl syndrome (BBS)
  • Retinitis pigmentosa (RP)
Novel CRYBG3 crystallin beta-gamma domain containing 3
Novel DHFR2 dihydrofolate reductase 2
  • Metabolism of folate and pterines
  • 5-Chloryl-2,4,6-quinazolinetriamine
  • 5-[4-Tert-Butylphenylsulfanyl]-2,4-Quinazolinediamine
  • 5-(4-Morpholin-4-Yl-Phenylsulfanyl)-2,4-Quinazolinediamine
  • 5-(4-Methoxyphenoxy)-2,4-Quinazolinediamine
  • 5-Phenylsulfanyl-2,4-Quinazolinediamine
  • 5-[(4-Methylphenyl)Sulfanyl]-2,4-Quinazolinediamine
  • 7-(1-ETHYL-PROPYL)-7H-PYRROLO-[3,2-F]QUINAZOLINE-1,3-DIAMINE
  • 7-[2-METHOXY-1-(METHOXYMETHYL)ETHYL]-7H-PYRROLO[3,2-F] QUINAZOLINE-1,3-DIAMINE
  • Epigallocatechin gallate
Novel RIOX2 ribosomal oxygenase 2
  • HDMs demethylate histones
ACSF2 acyl-CoA synthetase family member 2
  • Mitochondrial Fatty Acid Beta-Oxidation
AIG1 androgen induced 1
ALG3 ALG3 alpha-1,3- mannosyltransferase
  • Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein
  • Defective ALG3 causes ALG3-CDG (CDG-1d)
  • Congenital disorders of glycosylation (CDG) type I
ANKRD46 ankyrin repeat domain 46
AOC3 amine oxidase copper containing 3
  • Phase I - Functionalization of compounds
  • Phenelzine
  • Hydralazine
  • 6-hydroxydopa quinone
AQP10 aquaporin 10
  • Passive transport by Aquaporins
B4GALNT2 beta-1,4-N-acetyl-galactosaminyltransferase 2
  • Asparagine N-linked glycosylation
  • Lewis blood group biosynthesis
BMP10 bone morphogenetic protein 10
  • Signaling by BMP
  • Molecules associated with elastic fibres
BNIP3 BCL2 interacting protein 3
BRICD5 BRICHOS domain containing 5
C1GALT1 core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1
  • Defective C1GALT1C1 causes Tn polyagglutination syndrome (TNPS)
  • O-linked glycosylation of mucins
C2CD2L C2CD2 like
C4orf3 chromosome 4 open reading frame 3
CCDC167 coiled-coil domain containing 167
CCL4 C-C motif chemokine ligand 4
  • Chemokine receptors bind chemokines
  • G alpha (i) signalling events
  • Interleukin-10 signaling
CCL4L2 C-C motif chemokine ligand 4 like 2
  • G alpha (i) signalling events

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