ECT2 and TCEB1

  • Number of citations of the paper that reports this interaction (PMID 22990118)
  • 7
  • Data Source:
  • BioGRID (two hybrid)

ECT2

TCEB1

Gene Name epithelial cell transforming 2 transcription elongation factor B (SIII), polypeptide 1 (15kDa, elongin C)
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Attention deficit hyperactivity disorder ( 20732625)
Protein-Protein Interactions 37 interactors: ABR C2orf42 CCDC91 CD19 CDK1 CHST10 COX2 CRIPAK CSTB EIF4A2 EIF5B ERAL1 F2RL2 FANCM GGN ILVBL KLHL20 MBD1 MT2A NOMO1 NPC2 OOSP2 OTUB1 PARD6A PCOLCE PLK1 POMP PSMA6 RACGAP1 RHOG RPS20 SNRNP200 SPATA22 TCEB1 THAP11 UBB VDAC2 34 interactors: ASB6 CBX5 CENPC COMMD1 CPTP CUL2 CUL3 CUL5 CYP2J2 ECT2 EFNB3 GNB2L1 JTB LRRC41 MCM7 MED8 METTL21C MRAS NOTCH4 PRAME RCAN2 RNF7 SAT2 SERTAD1 SOCS1 SOCS3 SOCS6 TCEB2 TCEB3B TCEB3C USP33 VHL WNT7B ZYG11B
Entrez ID 1894 6921
HPRD ID 11860 02875
Ensembl ID ENSG00000114346 ENSG00000154582
Uniprot IDs G5E9L8 Q9H8V3 Q15369
PDB IDs 3L46 1LM8 1LQB 1VCB 2C9W 2IZV 3DCG 3ZKJ 3ZRC 3ZRF 3ZTC 3ZTD 3ZUN 4AJY 4AWJ 4B95 4B9K
Enriched GO Terms of Interacting Partners?
Tagcloud ?
broader  correlate  correlates  cytoskeleton  dbl  dbs  deregulated  encodes  exchange  family  gtpases  guanine  jun  lfc  lsc  mpk2  nh2  oncogenes  panel  possess  rho  sets  specificities  structurally  transformed  transforming  utilization  versions  weakly 
adrenal  arise  bc  chromaffin  cnl  copy  cul2  disrupting  elongin  enrichment  harbored  heterozygosity  hif1  hif1a  hippel  hypoxic  indeed  inherited  lindau  merit  normoxic  pcc  pheochromocytomas  predisposing  pseudohypoxic  rbx1  tceb2  vhl  von 
Tagcloud (Difference) ?
broader  correlate  correlates  cytoskeleton  dbl  dbs  deregulated  encodes  exchange  family  gtpases  guanine  jun  lfc  lsc  mpk2  nh2  oncogenes  panel  possess  rho  sets  specificities  structurally  transformed  transforming  utilization  versions  weakly 
adrenal  arise  bc  chromaffin  cnl  copy  cul2  disrupting  elongin  enrichment  harbored  heterozygosity  hif1  hif1a  hippel  hypoxic  indeed  inherited  lindau  merit  normoxic  pcc  pheochromocytomas  predisposing  pseudohypoxic  rbx1  tceb2  vhl  von 
Tagcloud (Intersection) ?