AP1M1 and DCX

  • Number of citations of the paper that reports this interaction (PMID 11591131)
  • 10
  • Data Source:
  • HPRD (two hybrid, in vitro)

AP1M1

DCX

Gene Name adaptor-related protein complex 1, mu 1 subunit doublecortin
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 29 interactors: ACD AP1M1 AP2M1 APP CALCOCO2 CDK5 FBXO25 GOLGA2 IKZF1 KIFC3 KRT40 KRTAP10-8 MEOX1 MID2 NFASC PAFAH1B1 POT1 PPP1CA PPP1R9B RINT1 SPAG5 SPP1 TERF1 TINF2 TRIM23 TRIM27 TRIM39 USP9X ZBTB5
Entrez ID 8907 1641
HPRD ID 04639 02127
Ensembl ID ENSG00000072958 ENSG00000077279
Uniprot IDs B3KNH5 E7ENJ6 Q59EK3 Q9BXS5 A8K340 B4DM53 O43602
PDB IDs 1MJD 2BQQ 2XRP 4ATU
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  classical  deletions  disrupt  epilepsy  frontal  gradient  lis  lis1  lissencephaly  malformation  mutations  occipital  overlapping  parietal  proline  q23  repeats  retardation  sequencing  sexes  southern  splice  sporadic  though  truncation  wd40  xlis  xq22 
Tagcloud (Difference) ?
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  classical  deletions  disrupt  epilepsy  frontal  gradient  lis  lis1  lissencephaly  malformation  mutations  occipital  overlapping  parietal  proline  q23  repeats  retardation  sequencing  sexes  southern  splice  sporadic  though  truncation  wd40  xlis  xq22 
Tagcloud (Intersection) ?