IMMP2L and HNRNPD

  • Number of citations of the paper that reports this interaction (PMID 15231747)
  • 44
  • Data Source:
  • BioGRID (two hybrid)

IMMP2L

HNRNPD

Gene Name IMP2 inner mitochondrial membrane peptidase-like (S. cerevisiae) heterogeneous nuclear ribonucleoprotein D (AU-rich element RNA binding protein 1, 37kDa)
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 1 interactors: HNRNPD 92 interactors: ABCC10 ACTB ARF4 B3GAT3 BCL2 BET1L BRCA1 C1QBP CAPN1 CD81 CD97 CINP COG7 COL18A1 CSDE1 CTSB CUTA DGCR2 DHX30 EEF2 EIF4G1 ERG EXOSC4 FBXL15 FLNA GSK3B GTF3C3 GTSE1 GUK1 HBZ HDAC1 HIRA HMGA1 HNRNPC HNRNPF HNRNPH3 HNRNPK HNRNPU HSPA4 HSPB1 HSPB2 IGF2BP2 IL7R IMMP2L IMMT ING4 LDHA LSM5 MAP2K1 MAPK6 MEOX2 MPP1 MTA2 MYC NTMT1 P4HB PABPC1 PCBP1 PCBP2 PCSK7 PDLIM7 PEX10 PPOX PRDX3 PRKACA PTBP2 PYCR1 RALY RPSA SAFB SDF2 SEPT9 SF3B4 SFN SHISA5 SLC27A5 SLC3A2 SNAPC4 SNRPC SREK1 SUMO4 SYNCRIP TMEM261 TNPO1 TRN-GTT2-1 TSEN34 U2AF2 UBE2I UQCRC1 VEGFA VHL YBX1
Entrez ID 83943 3184
HPRD ID 07297 03206
Ensembl ID ENSG00000184903
Uniprot IDs A4D0S9 Q96T52 Q14103
PDB IDs 1HD0 1HD1 1IQT 1WTB 1X0F 2Z5N
Enriched GO Terms of Interacting Partners?
Tagcloud ?
7q31  array  autistic  behavioural  cgh  copy  cytochromes  deficit  description  disorders  encodes  gilles  hyperactivity  inner  inside  la  microdeletion  microduplication  neurodevelopmental  neurological  overlapping  penetrance  phenotypic  protease  retardation  tourette  unrelated  variations  workup 
abcb7  advance  alas2  asxl1  bclaf1  brca1  causal  cbl  cd34  december  deregulation  disruption  doi  erythroid  exon  leu  link  online  pathophysiology  prpf8  publication  rars  refractory  sf3b1  sideroblasts  slc25a37  splicing  transcript  transcriptome 
Tagcloud (Difference) ?
7q31  array  autistic  behavioural  cgh  copy  cytochromes  deficit  description  disorders  encodes  gilles  hyperactivity  inner  inside  la  microdeletion  microduplication  neurodevelopmental  neurological  overlapping  penetrance  phenotypic  protease  retardation  tourette  unrelated  variations  workup 
abcb7  advance  alas2  asxl1  bclaf1  brca1  causal  cbl  cd34  december  deregulation  disruption  doi  erythroid  exon  leu  link  online  pathophysiology  prpf8  publication  rars  refractory  sf3b1  sideroblasts  slc25a37  splicing  transcript  transcriptome 
Tagcloud (Intersection) ?