MED13L and FBXW7

  • Number of citations of the paper that reports this interaction (PMID 23322298)
  • 8
  • Data Source:
  • BioGRID (enzymatic study)

MED13L

FBXW7

Gene Name mediator complex subunit 13-like F-box and WD repeat domain containing 7, E3 ubiquitin protein ligase
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 2 interactors: FBXW7 MED13 33 interactors: ARL6IP1 CCNE1 CCNE2 CDC34 CREB3L1 CREB3L2 CUL1 EBNA1BP2 FAM101A GLMN GNB2L1 HEY1 HIPK2 JUN KIAA1875 KLF5 LINGO1 MCL1 MED13 MED13L MMS22L MYB MYC NOTCH1 NOTCH4 PARK2 PPARGC1A PSEN1 SHPRH SKP1 STOML1 SUMF2 UBE2D1
Entrez ID 23389 55294
HPRD ID 10579 05888
Ensembl ID ENSG00000123066 ENSG00000109670
Uniprot IDs Q71F56 B7Z2C8 G0Z2K0 Q969H0 S4R3U4
PDB IDs 2OVP 2OVQ 2OVR
Enriched GO Terms of Interacting Partners?
Tagcloud ?
16p11  17q21  2p21  acot7  autism  auts2  cask  categorised  cnvs  crebbp  ctnnd2  delineating  exonic  grm8  homozygous  incidental  instrumental  iq  kb  microdeletion  morbid  ndds  neurodevelopmental  nrxn3  omim  pafah1b1  satb2  sizing  undiagnosed 
bcl11b  cadherin  discovered  dnm2  druggable  exhibitedthe  fat1  frequencies  guide  harboured  herc1  jak  jak3  lymphoblastic  mll2  mutational  notch1  notch2  phf6  recurrent  regulators  reln  secretase  splicing  subclonal  unfavourable  warranted  wt1  zrsr2 
Tagcloud (Difference) ?
16p11  17q21  2p21  acot7  autism  auts2  cask  categorised  cnvs  crebbp  ctnnd2  delineating  exonic  grm8  homozygous  incidental  instrumental  iq  kb  microdeletion  morbid  ndds  neurodevelopmental  nrxn3  omim  pafah1b1  satb2  sizing  undiagnosed 
bcl11b  cadherin  discovered  dnm2  druggable  exhibitedthe  fat1  frequencies  guide  harboured  herc1  jak  jak3  lymphoblastic  mll2  mutational  notch1  notch2  phf6  recurrent  regulators  reln  secretase  splicing  subclonal  unfavourable  warranted  wt1  zrsr2 
Tagcloud (Intersection) ?