SMARCC2 and SRGAP3

  • Number of citations of the paper that reports this interaction (PMID 12368262)
  • 35
  • Data Source:
  • HPRD (in vivo)

SMARCC2

SRGAP3

Gene Name SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2 SLIT-ROBO Rho GTPase activating protein 3
Image No pdb structure No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 21 interactors: ARRB2 ATXN1 ATXN1L BAZ1B C11orf74 CSNK2A1 GATA1 ITCH ITSN1 KLF1 MCPH1 NOVA1 PEX14 PHYHIP POLR2C RAB1B RELB SP1 SRGAP3 TERF1 TERF2IP 9 interactors: DISC1 DTNBP1 FASLG KDM1A PRMT6 SMARCC2 SUV39H1 TNIK WASF1
Entrez ID 6601 9901
HPRD ID 03437 12108
Ensembl ID ENSG00000139613 ENSG00000196220
Uniprot IDs F8VXC8 Q8TAQ2 O43295
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?
affymetrix  arrays  c10orf18  cabp4  capn10  centb1  converted  fdr  fractioned  genechip  glycerol  hybridized  or4c6  papillary  ran  sall1  serous  spata13  splicing  st  st18  subcellular  supernatants  supraspliceosome  transcriptome  wdr78  znf263  zp2  zranb2 
3p  anomalies  arm  camk1  congenital  creld1  define  deleted  deletion  deletions  features  give  handicap  interstitial  involve  kb  lengths  mb  mtmr14  overlap  presents  prove  respect  rise  seizures  syndrome  tada3  terminus  typical 
Tagcloud (Difference) ?
affymetrix  arrays  c10orf18  cabp4  capn10  centb1  converted  fdr  fractioned  genechip  glycerol  hybridized  or4c6  papillary  ran  sall1  serous  spata13  splicing  st  st18  subcellular  supernatants  supraspliceosome  transcriptome  wdr78  znf263  zp2  zranb2 
3p  anomalies  arm  camk1  congenital  creld1  define  deleted  deletion  deletions  features  give  handicap  interstitial  involve  kb  lengths  mb  mtmr14  overlap  presents  prove  respect  rise  seizures  syndrome  tada3  terminus  typical 
Tagcloud (Intersection) ?