HNRNPC and FXR2

  • Number of citations of the paper that reports this interaction (PMID 16189514)
  • 699

HNRNPC

FXR2

Gene Name heterogeneous nuclear ribonucleoprotein C (C1/C2) fragile X mental retardation, autosomal homolog 2
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 48 interactors: AP1M1 BARD1 BRCA1 BRCA2 BRIP1 BTRC CCDC85B CDKN2A CELF1 CSNK1A1 CSNK2A1 CSNK2A2 DHX9 EPS8 ERG FAS FXR2 GRB2 HNRNPD IL7R KHDRBS3 KPNA2 KPNA3 KPNA4 KRAS LMO2 LMO3 PALB2 PDGFB PHKB PIN1 PRKDC PTBP2 RAD51 RALY RALYL RBM41 SDCBP SF3B2 SMARCD1 SREK1 SRPK2 SUMO1 SUMO1P1 UBE2I YWHAQ ZFYVE26 ZNF581 90 interactors: AMOTL2 AP1M1 AP2M1 ARL6IP1 BAZ2B BRCA1 BYSL C10orf62 C1orf35 CALCOCO2 CAMK2D CBS CCDC33 CCDC85B CDKL3 CEP44 CEP55 COIL CYFIP1 CYFIP2 DPPA2 EWSR1 FAM90A1 FBP1 FMR1 FTH1 FXR1 GKAP1 HMBOX1 HNRNPC KCNRG KCTD4 KIAA1217 KIF1A KRT20 KXD1 LASP1 LCMT1 LCP2 LDOC1 MBIP MCRS1 MEAF6 MFAP1 MIA3 MORF4L1 MRPL43 NCK2 NDN NECAB2 NIF3L1 NME1 NONO NT5C2 PAF1 PAICS PCBD1 PIM1 POM121 PRAM1 PSME3 PTS RABAC1 RALYL RBBP8 RBMX RBPMS RPIA RTN3 RTN4 SCEL SNAP23 SRPK2 SSSCA1 SYT6 SYTL4 TBC1D22B THAP1 TNNT1 TRAF2 TRIM23 TRIM29 TRIM37 TSC22D4 YES1 ZBTB22 ZBTB8A ZMAT2 ZNF451 ZSCAN1
Entrez ID 3183 9513
HPRD ID 01243 05629
Ensembl ID ENSG00000092199 ENSG00000129245
Uniprot IDs P07910 P51116
PDB IDs 1TXP 1WF2 3LN4 3H8Z
Enriched GO Terms of Interacting Partners?
Tagcloud ?
17th  2d  appreciation  coordinately  coupling  d  deep  dihydroxyvitamin  entitled  epigenome  exerts  expanded  extra  fine  hormones  issue  linking  locations  microrna  ribonucleoprotein  special  splicing  steroid  transcriptionally  tuning  vdr  vdre  vitamin  workshop 
17p13  adipocytes  array  cgh  disability  duplication  dysmorphic  encodes  encompassing  facial  fingers  fissures  glut4  hyperpigmentation  intellectual  mandible  nlgn2  nostrils  obesity  p13  palpebral  proposita  recognizable  referred  seizures  slc2a4  slender  tp53  upturned 
Tagcloud (Difference) ?
17th  2d  appreciation  coordinately  coupling  d  deep  dihydroxyvitamin  entitled  epigenome  exerts  expanded  extra  fine  hormones  issue  linking  locations  microrna  ribonucleoprotein  special  splicing  steroid  transcriptionally  tuning  vdr  vdre  vitamin  workshop 
17p13  adipocytes  array  cgh  disability  duplication  dysmorphic  encodes  encompassing  facial  fingers  fissures  glut4  hyperpigmentation  intellectual  mandible  nlgn2  nostrils  obesity  p13  palpebral  proposita  recognizable  referred  seizures  slc2a4  slender  tp53  upturned 
Tagcloud (Intersection) ?