Search Results for: CD79A

183 interactions involving CD79A - CD79a molecule found:

Sort by: Symbol Number of Pathways Number of Drugs Number of Diseases
Novel Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
TMEM86A transmembrane protein 86A
TMEM86B transmembrane protein 86B
  • Acyl chain remodelling of PC
TMPPE transmembrane protein with metallophosphoesterase domain
TNFRSF10C TNF receptor superfamily member 10c
  • TP53 Regulates Transcription of Death Receptors and Ligands
TRAM1L1 translocation associated membrane protein 1 like 1
TRARG1 trafficking regulator of GLUT4 (SLC2A4) 1
TSNARE1 t-SNARE domain containing 1
TSPAN2 tetraspanin 2
TSPO2 translocator protein 2
UBE2J1 ubiquitin conjugating enzyme E2 J1
  • Antigen processing: Ubiquitination & Proteasome degradation
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
UNC93B1 unc-93 homolog B1, TLR signaling regulator
  • Trafficking and processing of endosomal TLR
  • UNC93B1 deficiency - HSE
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
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
VTI1B vesicle transport through interaction with t-SNAREs 1B
  • Platelet degranulation
WFDC2 WAP four-disulfide core domain 2
WFS1 wolframin ER transmembrane glycoprotein
  • XBP1(S) activates chaperone genes
  • Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
  • Post-translational protein phosphorylation
  • Type II diabetes mellitus
  • Wolfram syndrome (WFS); DIDMOAD syndrome
YIF1A Yip1 interacting factor homolog A, membrane trafficking protein
  • XBP1(S) activates chaperone genes
YIPF4 Yip1 domain family member 4

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