Search Results for: RETREG3

111 interactions involving RETREG3 - reticulophagy regulator family member 3 found:

Sort by: Symbol Number of Pathways Number of Drugs Number of Diseases
Novel Symbol Description Pathways Hide Drugs Hide Diseases Hide
TSNARE1 t-SNARE domain containing 1
TSPO2 translocator protein 2
UBIAD1 UbiA prenyltransferase domain containing 1
  • Metabolism of vitamin K
  • Schnyder corneal dystrophy (SCD); Schnyder crystalline corneal dystrophy (SCCD); Crystalline stromal dystrophy; Schnyder crystalline dystrophy sine crystals
VAMP1 vesicle associated membrane protein 1
  • Toxicity of botulinum toxin type D (botD)
  • Toxicity of botulinum toxin type F (botF)
  • Toxicity of botulinum toxin type G (botG)
  • Botulinum toxin type B
VAMP3 vesicle associated membrane protein 3
  • ER-Phagosome pathway
  • Retrograde transport at the Trans-Golgi-Network
  • Cargo recognition for clathrin-mediated endocytosis
  • Clathrin-mediated endocytosis
  • RHOA GTPase cycle
  • RHOB GTPase cycle
  • RHOC GTPase cycle
  • CDC42 GTPase cycle
  • RAC1 GTPase cycle
  • RAC2 GTPase cycle
  • RHOD GTPase cycle
  • RHOQ GTPase cycle
  • RHOH GTPase cycle
  • RHOG GTPase cycle
  • RHOJ GTPase cycle
  • RAC3 GTPase cycle
  • RHOF GTPase cycle
VAMP4 vesicle associated membrane protein 4
  • Retrograde transport at the Trans-Golgi-Network
  • Cargo recognition for clathrin-mediated endocytosis
  • Clathrin-mediated endocytosis
VAMP5 vesicle associated membrane protein 5
VAPA VAMP associated protein A
  • Sphingolipid de novo biosynthesis
  • Neutrophil degranulation
  • Insertion of tail-anchored proteins into the endoplasmic reticulum membrane
  • Insertion of tail-anchored proteins into the endoplasmic reticulum membrane
VAPB VAMP associated protein B and C
  • Sphingolipid de novo biosynthesis
  • RHOA GTPase cycle
  • RHOC GTPase cycle
  • RAC2 GTPase cycle
  • RHOD GTPase cycle
  • RHOG GTPase cycle
  • Spinal muscular atrophy (SMA), including: SMA type I (SMA1) / Werdning-Hoffman disease; SMA type II (SMA2); SMA type III (SMA3) / Kugeleberg-Welander disease; SMA type IV (SMA4); X-linked SMA 2 (SMAX2); X-linked distal SMA 3 (DSMAX); Distal SMA autosomal recessive type 4 (DSMA4); Congenital distal spinal muscular atrophy (SMAL); SMA proximal adult autosomal dominant (SMAPAD)
  • Amyotrophic lateral sclerosis (ALS); Lou Gehrig's disease
YIPF1 Yip1 domain family member 1
YIPF6 Yip1 domain family member 6
  • Golgi Associated Vesicle Biogenesis

Page 6 out of 6 pages