POM121 and FXR2

  • Number of citations of the paper that reports this interaction (PMID 25416956)
  • 0
  • Data Source:
  • BioGRID (two hybrid)

POM121

FXR2

Gene Name POM121 transmembrane nucleoporin fragile X mental retardation, autosomal homolog 2
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Subcutaneous adipose tissue ( 22589738)
Protein-Protein Interactions 21 interactors: AGR2 AP2B1 APC ATXN1 BRCA1 CEP55 CEP76 CLDN3 COL4A3BP FXR2 GFAP GOLGA2 GYG1 HOMER3 LPXN NFKBIA PAXIP1 RBPMS TEX11 TRIM23 TRIP6 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 9883 9513
HPRD ID 11448 05629
Ensembl ID ENSG00000196313 ENSG00000129245
Uniprot IDs Q96HA1 P51116
PDB IDs 3H8Z
Enriched GO Terms of Interacting Partners?
Tagcloud ?
antagonize  brd1  brings  childhood  chimeric  comprise  dach1  encoding  fluorescence  frame  fusion  fusions  hipk1  hybridization  identification  implicated  least  leukemia  lymphoblastic  master  occur  partner  pax5  precursor  rearrangements  regulator  situ  transduction  tumorigenesis 
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) ?
antagonize  brd1  brings  childhood  chimeric  comprise  dach1  encoding  fluorescence  frame  fusion  fusions  hipk1  hybridization  identification  implicated  least  leukemia  lymphoblastic  master  occur  partner  pax5  precursor  rearrangements  regulator  situ  transduction  tumorigenesis 
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) ?