RBMX and FXR2

  • Number of citations of the paper that reports this interaction (PMID 16189514)
  • 699
  • Data Source:
  • HPRD (two hybrid)

RBMX

FXR2

Gene Name RNA binding motif protein, X-linked fragile X mental retardation, autosomal homolog 2
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 34 interactors: APOBEC3C CCDC33 CIRBP CLK3 CSNK2A1 FAM103A1 FUS FXR2 HNRNPK IL7R ITSN2 JAK2 KHDRBS1 KHDRBS2 KHDRBS3 LNX1 MAGOHB NABP1 NFE2L2 PRR3 PSMF1 RBM3 RBM7 RBMY1A1 RBMY1F ROBO3 SNRPA SOCS3 SORBS3 SREK1 STAT5A TRA2B XRN1 ZNF490 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 27316 9513
HPRD ID 02186 05629
Ensembl ID ENSG00000147274 ENSG00000129245
Uniprot IDs P38159 P51116
PDB IDs 3H8Z
Enriched GO Terms of Interacting Partners?
Tagcloud ?
122c  2012cb944901  9qh  azoospermia  blimp1  dazl  ddx4  declare  dppa3  envisioned  fam122c  funds  grants  hef  ikbkg  ipsc  ipscs  lin28  poi  poi1  poi2  prdm1  q26  stella  sublines  talents  vasa  xq  znf 
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) ?
122c  2012cb944901  9qh  azoospermia  blimp1  dazl  ddx4  declare  dppa3  envisioned  fam122c  funds  grants  hef  ikbkg  ipsc  ipscs  lin28  poi  poi1  poi2  prdm1  q26  stella  sublines  talents  vasa  xq  znf 
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) ?