AP1M1 and FXR2

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

AP1M1

FXR2

Gene Name adaptor-related protein complex 1, mu 1 subunit 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 43 interactors: AP1B1 AP1M2 AP2B1 BRCA1 CEP57L1 CORO7 CTLA4 DCX DVL2 DZIP3 EHD2 ETV6 FAM9B FXR2 GAK GRIN2A GRIN2B HNRNPC HOOK2 IKZF1 KIF13A KRT40 KRTAP10-3 KRTAP10-7 LAMP1 LDOC1 LZTS2 MTF1 PHC2 PIGR PNMA5 RUNDC3A SDCCAG3 SELP SSX2IP TGOLN2 TIFA TNIP1 VAMP4 ZBTB14 ZBTB43 ZBTB44 ZBTB8A 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 8907 9513
HPRD ID 04639 05629
Ensembl ID ENSG00000072958 ENSG00000129245
Uniprot IDs B3KNH5 E7ENJ6 Q59EK3 Q9BXS5 P51116
PDB IDs 3H8Z
Enriched GO Terms of Interacting Partners?
Tagcloud ?
19p13  adaptor  ap1m2  ap2m1  chromosome  clathrin  cloned  closely  distantly  diverged  duplication  except  exclusively  fact  genomic  homolog  identical  insertion  intron  introns  mapped  mu1a  mu1b  mu2  positions  proximal  separation  similarity  syntenic 
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) ?
19p13  adaptor  ap1m2  ap2m1  chromosome  clathrin  cloned  closely  distantly  diverged  except  exclusively  fact  genomic  homolog  identical  insertion  intron  introns  mapped  mu1a  mu1b  mu2  positions  proximal  separation  similarity  syntenic 
17p13  adipocytes  array  cgh  disability  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) ?
duplication