RTN3 and FXR2

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

RTN3

FXR2

Gene Name reticulon 3 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 15 interactors: CDIPT COL4A3BP FAM160A2 FGFR1 FXR2 PLEKHF2 PPP2R3C PTPN9 RAB33A RTN4 SNX1 SPOP TERF1 UGCG ZNF391 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 10313 9513
HPRD ID 18516 05629
Ensembl ID ENSG00000133318 ENSG00000129245
Uniprot IDs O95197 P51116
PDB IDs 3H8Z
Enriched GO Terms of Interacting Partners?
Tagcloud ?
address  affects  alzheimer  bace1  brains  contributing  deficiency  deposition  discernible  elevation  endoplasmic  facilitates  generating  grow  intriguing  lasting  monomer  morphological  negatively  normally  null  obviously  phenotypes  question  reticulon  secretase  shaping  supporting  tubular 
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) ?
address  affects  alzheimer  bace1  brains  contributing  deficiency  deposition  discernible  elevation  endoplasmic  facilitates  generating  grow  intriguing  lasting  monomer  morphological  negatively  normally  null  obviously  phenotypes  question  reticulon  secretase  shaping  supporting  tubular 
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) ?