Search Results for: RETREG3

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

Sort by: Symbol Number of Pathways Number of Drugs Number of Diseases
Novel Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
TMPPE transmembrane protein with metallophosphoesterase domain
TPRG1 tumor protein p63 regulated 1
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
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
  • 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

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