Search Results for: NDRG4

Novel Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
LIME1 Lck interacting transmembrane adaptor 1
LRRC59 leucine rich repeat containing 59
MAL2 mal, T cell differentiation protein 2
MTIF3 mitochondrial translational initiation factor 3
  • Mitochondrial translation initiation
PLP2 proteolipid protein 2
PRAF2 PRA1 domain family member 2
RABAC1 Rab acceptor 1
REEP6 receptor accessory protein 6
  • Olfactory Signaling Pathway
RTN3 reticulon 3
  • Synaptic adhesion-like molecules
SCAMP1 secretory carrier membrane protein 1
  • Neutrophil degranulation
SDR16C5 short chain dehydrogenase/reductase family 16C member 5
  • RA biosynthesis pathway
SFT2D2 SFT2 domain containing 2
SGK1 serum/glucocorticoid regulated kinase 1
  • Stimuli-sensing channels
  • Regulation of TP53 Degradation
  • Transcriptional Regulation by MECP2
  • NGF-stimulated transcription
  • Flavin mononucleotide
  • [4-(5-naphthalen-2-yl-1H-pyrrolo[2,3-b]pyridin-3-yl)phenyl]acetic acid
  • 4-(5-phenyl-1H-pyrrolo[2,3-b]pyridin-3-yl)benzoic acid
SIN3A SIN3 transcription regulator family member A
  • SUMOylation of transcription cofactors
  • Regulation of lipid metabolism by PPARalpha
  • NoRC negatively regulates rRNA expression
  • RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function
  • Loss of MECP2 binding ability to 5mC-DNA
  • Regulation of MECP2 expression and activity
  • MECP2 regulates neuronal receptors and channels
  • MECP2 regulates transcription of neuronal ligands
  • FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes
  • Factors involved in megakaryocyte development and platelet production
SMPD2 sphingomyelin phosphodiesterase 2
  • Glycosphingolipid metabolism
  • Ceramide signalling
  • TNFR1-mediated ceramide production
SYNGR1 synaptogyrin 1
  • Neutrophil degranulation
SYNGR3 synaptogyrin 3
SYP synaptophysin
  • Syndromic X-linked mental retardation with epilepsy or seizures, including: West syndrome (WS); Partington syndrome (PRTS); Proud syndrome (ACCAG); XMR and epilepsy (XMRE); MRXHF1; XMR OPHN1-related (MRXSO) ; XELBD; XMR, Christianson type (MRXSC); Creatine deficiency syndrome (XL-CDS); Renpenning syndrome (RENS1); Epilepsy and mental retardation limited to females (EFMR); Periventricular nodular heterotopia (PVNH); Hydrocephalus (XLH); XMR, JARID1C related (MRXSJ); Boerjeson-Forssman syndrome (BFLS); CK syndrome (CKS)
THAP4 THAP domain containing 4
TMEM208 transmembrane protein 208

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