Search Results for: FBN1

26 interactions involving FBN1 - fibrillin 1 found:

Sort by: Symbol Number of Pathways Number of Drugs Number of Diseases
Novel Symbol Description Pathways Hide Drugs Hide Diseases Hide
MFAP2 microfibril associated protein 2
  • Elastic fibre formation
  • Molecules associated with elastic fibres
  • Molecules associated with elastic fibres
MFAP5 microfibril associated protein 5
  • Elastic fibre formation
  • Molecules associated with elastic fibres
  • Molecules associated with elastic fibres
MYOC myocilin
  • Primary open angle glaucoma
SGTB small glutamine rich tetratricopeptide repeat co-chaperone beta
SPRY2 sprouty RTK signaling antagonist 2
  • Spry regulation of FGF signaling
  • EGFR downregulation
VCAN versican
  • Glycosaminoglycan-protein linkage region biosynthesis
  • CS-GAG biosynthesis
  • DS-GAG biosynthesis
  • CS/DS degradation
  • ECM proteoglycans
  • Defective B4GALT7 causes EDS, progeroid type
  • Defective B3GAT3 causes JDSSDHD
  • Defective CHST3 causes SEDCJD
  • Defective CHST14 causes EDS, musculocontractural type
  • Defective CHSY1 causes TPBS
  • Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
  • Defective B3GALT6 causes EDSP2 and SEMDJL1
  • Post-translational protein phosphorylation
  • Hyaluronic acid
  • Vitreoretinal degeneration, including: Stickler syndrome type I (STL1); Stickler syndrome type II (STL2); Snowflake vitreoretinal degeneration (SVD); Wagner syndrome 1 (WGN1); Knobloch syndrome (KNO); Enhanced S-cone syndrome (ESCS); Autosomal dominant vitreoretinochoroidopathy (ADVIRC)

Page 2 out of 2 pages