Search Results for: TCF4

235 interactions involving TCF4 - transcription factor 4 found:

Sort by: Symbol Number of Pathways Number of Drugs Number of Diseases
Novel Interactant Symbol Name
Associated Pathways
Binding Drugs
Associated Diseases
SCX scleraxis bHLH transcription factor
SDCBP syndecan binding protein
  • Ephrin signaling
  • Neurofascin interactions
  • RIPK1-mediated regulated necrosis
  • Regulation of necroptotic cell death
  • Neutrophil degranulation
SEC14L4 SEC14 like lipid binding 4
  • Vitamin E
SGF29 SAGA complex associated factor 29
  • HATs acetylate histones
SHFL shiftless antiviral inhibitor of ribosomal frameshifting
SIGLEC6 sialic acid binding Ig like lectin 6
  • Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell
SLC39A13 solute carrier family 39 member 13
  • Ehlers-Danlos syndrome (EDS), including: EDS classical type (EDS1/2); EDS hypermobility type (EDS3); EDS vascular type (EDS4); EDS kyphoscoliosis type (EDS6); EDS arthrochalasia type (EDS7A/7B); EDS dermatospraxis type (EDS7C); EDS autosomal recessive cardiac valvular form (EDSCV); EDS musculocontractural type (EDSMC); EDS progeroid form (EDSP); Tenascin-X deficiency (TNXD); Brittle cornea syndrome (EDS6B); EDS-like spondylocheiro dysplasia (SCD-EDS)
SLC4A1AP solute carrier family 4 member 1 adaptor protein
SMCP sperm mitochondria associated cysteine rich protein
SMG9 SMG9 nonsense mediated mRNA decay factor
  • Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC)
SMOC1 SPARC related modular calcium binding 1
SPATC1L spermatogenesis and centriole associated 1 like
SPG21 SPG21 abhydrolase domain containing, maspardin
  • Hereditary spastic paraplegia (SPG)
SPO11 SPO11 initiator of meiotic double stranded breaks
  • Meiotic recombination
SRSF2 serine and arginine rich splicing factor 2
  • Transport of Mature mRNA derived from an Intron-Containing Transcript
  • mRNA Splicing - Major Pathway
  • mRNA Splicing - Minor Pathway
  • mRNA 3'-end processing
  • RNA Polymerase II Transcription Termination
STAMBPL1 STAM binding protein like 1
  • Metalloprotease DUBs
STK16 serine/threonine kinase 16
  • Fostamatinib
STX11 syntaxin 11
  • Familial hemophagocytic lymphohistiocytosis (FHPL), including the following three diseases: Perforin deficiency; Munc deficiency; STX11 deficiency
SZT2 SZT2 subunit of KICSTOR complex
  • Amino acids regulate mTORC1
TAL1 TAL bHLH transcription factor 1, erythroid differentiation factor
  • RUNX1 regulates transcription of genes involved in differentiation of HSCs
  • Transcriptional regulation of granulopoiesis
  • Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia)

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