Search Results for: FKBP7

112 interactions involving FKBP7 - FKBP prolyl isomerase 7 found:

Sort by: Symbol Number of Pathways Number of Drugs Number of Diseases
Novel Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
IGFBP5 insulin like growth factor binding protein 5
  • Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
  • Post-translational protein phosphorylation
IRF2 interferon regulatory factor 2
  • Pyroptosis
  • Interferon gamma signaling
  • Interferon alpha/beta signaling
  • Factors involved in megakaryocyte development and platelet production
JOSD2 Josephin domain containing 2
  • Josephin domain DUBs
LAT linker for activation of T cells
  • GPVI-mediated activation cascade
  • Generation of second messenger molecules
LNPEP leucyl and cystinyl aminopeptidase
  • Endosomal/Vacuolar pathway
  • Translocation of SLC2A4 (GLUT4) to the plasma membrane
  • Antigen processing: Ubiquitination & Proteasome degradation
MAN2B2 mannosidase alpha class 2B member 2
  • Lysosomal oligosaccharide catabolism
MIEF2 mitochondrial elongation factor 2
MRM1 mitochondrial rRNA methyltransferase 1
  • rRNA modification in the mitochondrion
NFU1 NFU1 iron-sulfur cluster scaffold
  • Protein lipoylation
NKG7 natural killer cell granule protein 7
NPFFR2 neuropeptide FF receptor 2
  • Orexin and neuropeptides FF and QRFP bind to their respective receptors
  • G alpha (q) signalling events
OCIAD1 OCIA domain containing 1
OXNAD1 oxidoreductase NAD binding domain containing 1
PBX3 PBX homeobox 3
PCYT1A phosphate cytidylyltransferase 1A, choline
  • Synthesis of PC
  • Choline
  • Choline salicylate
PEX16 peroxisomal biogenesis factor 16
  • Class I peroxisomal membrane protein import
  • Class I peroxisomal membrane protein import
  • Zellweger syndrome spectrum, including: Zellweger syndrome (ZS); Adrenoleukodystrophy, neonatal (NALD); Infantile Refsum disease (IRD)
PEX19 peroxisomal biogenesis factor 19
  • ABC transporters in lipid homeostasis
  • Class I peroxisomal membrane protein import
  • Class I peroxisomal membrane protein import
  • Zellweger syndrome spectrum, including: Zellweger syndrome (ZS); Adrenoleukodystrophy, neonatal (NALD); Infantile Refsum disease (IRD)
PLLP plasmolipin
PLP1 proteolipid protein 1
  • Hypomyelinating leukodystrophy (HLD); Pelizaeus-Merzbacher disease (PMD)
  • Hereditary spastic paraplegia (SPG)
PLP2 proteolipid protein 2

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