FXR2 and NCK2

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

FXR2

NCK2

Gene Name fragile X mental retardation, autosomal homolog 2 NCK adaptor protein 2
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 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 80 interactors: ABI1 ABI2 ABI3 ARHGAP32 ATN1 AXIN1 AXL BCL11A CBLB CCDC33 CD3E CHN1 CPSF6 CPSF7 DDR1 DNM1 DOCK1 DOK1 DRAP1 DVL1 EEF1G EFHC2 EFNB1 EFNB2 EGFR EIF3H ERBB2 ERBB3 FAM53C FASLG FCRL2 FGFR1 FXR2 HNRNPK HOMEZ HOXC4 ILK IRS1 KHDRBS1 KIAA1217 LCP2 LIMS1 LNX1 LRRIQ3 LZTS2 MAGEA6 MASP1 MEOX2 NCKIPSD NPHS1 NR5A1 NTRK2 PAK1 PDGFRB PKN2 PRR20A PSMD10 PTK2 RASSF7 RBM26 REL SF3B4 SORBS2 SOS1 SPRY2 SRPK1 SRPK2 SYNPO TCF4 TNR TRIM27 TRIM41 TRIP6 VARS2 VPS37B WAS WASL WBP11 WIPF2 ZBTB7B
Entrez ID 9513 8440
HPRD ID 05629 05378
Ensembl ID ENSG00000129245 ENSG00000071051
Uniprot IDs P51116 E7ERP6 O43639
PDB IDs 3H8Z 1U5S 1WX6 1Z3K 2B86 2CIA 2FRW 2FRY 2JXB 4E6R
Enriched GO Terms of Interacting Partners?
Tagcloud ?
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 
accumulates  adapter  atr  becoming  cleavage  coordination  cytoskeletal  depleted  depletion  discrete  hela  hyperactive  increasingly  interconnectedness  interconnectivity  irradiation  monitored  mostly  nck1  parp  phenocopies  redundant  shortly  socs7  strikingly  translocation  undergo  uv 
Tagcloud (Difference) ?
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 
accumulates  adapter  atr  becoming  cleavage  coordination  cytoskeletal  depleted  depletion  discrete  hela  hyperactive  increasingly  interconnectedness  interconnectivity  irradiation  monitored  mostly  nck1  parp  phenocopies  redundant  shortly  socs7  strikingly  translocation  undergo  uv 
Tagcloud (Intersection) ?