Search Results for: REL

325 interactions involving REL - REL proto-oncogene, NF-kB subunit found:

Sort by: Symbol Number of Pathways Number of Drugs Number of Diseases
Novel Symbol Description Pathways Hide Drugs Hide Diseases Hide
TSTD2 thiosulfate sulfurtransferase like domain containing 2
TTC19 tetratricopeptide repeat domain 19
  • Complex III assembly
  • Mitochondrial respiratory chain deficiencies (MRCD), including: Mitochondrial complex I deficiency (MT-C1D); Complex II deficiency (MT-C2D); Complex III deficiency (MT-C3D); Complex IV deficiency (MT-C4D); Complex V deficiency (MT-ATPSD); Leigh syndrome (LS); Kearns-Sayre Syndrome (KSS); LCHD deficiency (LCHD); Leber Hereditary Optic Neuropathy (LHON); Myoclonic Epilepsy and Ragged-Red Fiber Disease (MERRF); NARP; MELAS; ACAD9 deficiency; HADH deficiency; HIBCH deficiency; GRACILE syndrome
TTC21A tetratricopeptide repeat domain 21A
TXNL4B thioredoxin like 4B
UBASH3A ubiquitin associated and SH3 domain containing A
UBASH3B ubiquitin associated and SH3 domain containing B
UBE2D4 ubiquitin conjugating enzyme E2 D4
  • Antigen processing: Ubiquitination & Proteasome degradation
UBE2K ubiquitin conjugating enzyme E2 K
  • Synthesis of active ubiquitin: roles of E1 and E2 enzymes
  • Negative regulators of DDX58/IFIH1 signaling
  • Antigen processing: Ubiquitination & Proteasome degradation
UBE2Z ubiquitin conjugating enzyme E2 Z
  • Synthesis of active ubiquitin: roles of E1 and E2 enzymes
  • Antigen processing: Ubiquitination & Proteasome degradation
UBXN7 UBX domain protein 7
  • Neddylation
  • KEAP1-NFE2L2 pathway
VPS25 vacuolar protein sorting 25 homolog
  • Endosomal Sorting Complex Required For Transport (ESCRT)
  • HCMV Late Events
WNK3 WNK lysine deficient protein kinase 3
  • Stimuli-sensing channels
YARS1 tyrosyl-tRNA synthetase 1
  • Cytosolic tRNA aminoacylation
  • Tyrosine
  • Beta-(2-Naphthyl)-Alanine
  • Resveratrol
  • Tyrosinal
  • N6-ISOPENTENYL-ADENOSINE-5'-MONOPHOSPHATE
  • p-Benzoyl-L-phenylalanine
  • 4-(2,2,2-TRIFLUOROETHYL)-L-PHENYLALANINE
  • Charcot-Marie-Tooth disease (CMT); Hereditary motor and sensory neuropathy; Peroneal muscular atrophy
YJU2 YJU2 splicing factor homolog
  • mRNA Splicing - Major Pathway
ZBTB16 zinc finger and BTB domain containing 16
  • Neddylation
  • Antigen processing: Ubiquitination & Proteasome degradation
  • Skeletal defects, genital hypoplasia, and mental retardation
  • Acute myeloid leukemia (AML)
ZDHHC24 zDHHC palmitoyltransferase 24
ZIC1 Zic family zinc finger 1
  • Specification of the neural plate border
  • Transcriptional and post-translational regulation of MITF-M expression and activity
ZNF417 zinc finger protein 417
  • Generic Transcription Pathway
ZNF446 zinc finger protein 446
  • Generic Transcription Pathway
ZNF550 zinc finger protein 550
  • Generic Transcription Pathway

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