GRM8 and FLNA

  • Number of citations of the paper that reports this interaction (PMID 11943148)
  • 9
  • Data Source:
  • HPRD (two hybrid, in vivo)

GRM8

FLNA

Gene Name glutamate receptor, metabotropic 8 filamin A, alpha
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Carotid atherosclerosis in HIV infection ( 20009918)
  • Chemerin levels ( 20237162)
  • Depression (quantitative trait) ( 20800221)
Protein-Protein Interactions 4 interactors: FLNA GPRASP1 PIAS1 PIAS2 82 interactors: ADAMTSL4 APC AR ARHGAP24 ARRB1 ARRB2 ASB2 BRCA2 CALCR CAMK2G CASR CAV1 CCNB1 CDC42 CEACAM1 CMIP DCN DRD1 DRD2 DRD3 ERBB3 F3 FABP1 FAM101A FBLIM1 FILIP1 FLNB FURIN GP1BA GRIK1 GRIK3 GRM4 GRM5 GRM7 GRM8 HNRNPD HSPB7 ITGB1 ITGB3 ITGB5 ITGB6 ITGB7 KCNE4 KCNJ2 KLHL12 LGALS14 LMNA MAP2K4 MAPK14 MTNR1A MTNR1B MYOT NPHP1 OPRM1 PAK1 PCBP2 PRKCA PSEN1 PSEN2 RAC1 RALA REL RHOA SELE SH2B3 SHBG SIGLEC10 SMAD3 SMAD5 SRC SVIL SYNPO2 TCF4 TLR10 TNIP2 TRAF2 TRIM55 TRIO TTN USP19 VHL YWHAG
Entrez ID 2918 2316
HPRD ID 03071 02060
Ensembl ID ENSG00000179603 ENSG00000196924
Uniprot IDs O00222 P21333 Q60FE5 Q6NXF2
PDB IDs 2AAV 2BP3 2BRQ 2J3S 2JF1 2K3T 2K7P 2K7Q 2W0P 2WFN 3CNK 3HOC 3HOP 3HOR 3ISW 3RGH
Enriched GO Terms of Interacting Partners?
Tagcloud ?
16p11  17q21  2p21  acot7  autism  auts2  cask  categorised  cnvs  crebbp  ctnnd2  delineating  exonic  homozygous  incidental  instrumental  iq  kb  med13l  microdeletion  morbid  ndds  neurodevelopmental  nrxn3  omim  pafah1b1  satb2  sizing  undiagnosed 
actin  acts  aggregation  bilateral  calcineurin  cortical  cytoskeleton  defects  downregulation  heterotopia  isoforms  knockdown  lateral  lining  linking  malformation  migration  periventricular  ph  prevented  progenitor  radial  rcan1  rearrangement  regulators  shrna  underlie  upstream  ventricles 
Tagcloud (Difference) ?
16p11  17q21  2p21  acot7  autism  auts2  cask  categorised  cnvs  crebbp  ctnnd2  delineating  exonic  homozygous  incidental  instrumental  iq  kb  med13l  microdeletion  morbid  ndds  neurodevelopmental  nrxn3  omim  pafah1b1  satb2  sizing  undiagnosed 
actin  acts  aggregation  bilateral  calcineurin  cortical  cytoskeleton  defects  downregulation  heterotopia  isoforms  knockdown  lateral  lining  linking  malformation  migration  periventricular  ph  prevented  progenitor  radial  rcan1  rearrangement  regulators  shrna  underlie  upstream  ventricles 
Tagcloud (Intersection) ?