SPP1 and DCX

  • Number of citations of the paper that reports this interaction (PMID 22779921)
  • 1
  • Data Source:
  • BioGRID (two hybrid)

SPP1

DCX

Gene Name secreted phosphoprotein 1 doublecortin
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 88 interactors: ABCF3 ACP5 AFF4 AMOTL2 APOA1 ATP2A2 ATP5F1 BAG6 BRD3 C1RL C2orf50 CACNG4 CALM1 CC2D1B CD44 CEP162 CHD1 CISD2 CMTM3 COMMD1 COPS5 CSNK2A1 CSNK2A2 CTNNBL1 CYB5R3 DCX DNAJB1 DNTTIP2 DSEL EEF1A1 EIF3K EPAS1 F2 FTH1 GRIPAP1 HBA2 HMGN1 IGFBP5 ITGA5 ITGA9 ITGAV ITGB1 KCNIP1 LRRC4 MAP1A MAP1B MARCKS MEOX2 MMP3 MMP7 MPPED1 MRPL23 NACA NCKAP1 NCSTN PDLIM7 PEMT PEPD PLD3 PRKACB PRKCA PRKG1 RANBP9 RAPGEF2 RBBP6 RIMS4 RPL13 RPL15 RPL5 RPS13 SEC24C SGTA SLC39A6 SNAPIN SSB STAU1 STK39 TBC1D8 TMEM168 TMEM30A TPT1 TTC1 TUBB UBQLN4 USP42 USP8 ZNF638 ZNF804A 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 6696 1641
HPRD ID 01325 02127
Ensembl ID ENSG00000118785 ENSG00000077279
Uniprot IDs B7Z351 P10451 Q3LGB0 A8K340 B4DM53 O43602
PDB IDs 3CXD 3DSF 1MJD 2BQQ 2XRP 4ATU
Enriched GO Terms of Interacting Partners?
Tagcloud ?
able  acquisition  acts  carcinomas  cbx7  chemokine  contributing  counteracts  decreases  encoding  fact  hmga1b  inducing  interacting  interferes  involves  malignant  member  modulation  osteopontin  played  polycomb  progressively  relation  repressive  suppose  take  transcriptional  whose 
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) ?
able  acquisition  acts  carcinomas  cbx7  chemokine  contributing  counteracts  decreases  encoding  fact  hmga1b  inducing  interacting  interferes  involves  malignant  member  modulation  osteopontin  played  polycomb  progressively  relation  repressive  suppose  take  transcriptional  whose 
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) ?