GRIN1 and SYNGAP1

  • Number of citations of the paper that reports this interaction (PMID 10862698)
  • 203
  • Data Source:
  • HPRD (in vivo)

GRIN1

SYNGAP1

Gene Name glutamate receptor, ionotropic, N-methyl D-aspartate 1 synaptic Ras GTPase activating protein 1
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Post-traumatic stress disorder (asjusted for relatedness) ( 23726511)
Protein-Protein Interactions 53 interactors: ACTN2 AKAP9 CALM1 CAMK2A CAMK2G CANX CDH2 CIT CLTC CTNNB1 DLG2 DLG3 DLG4 DLGAP4 DNM1 DRD1 DUSP4 EPHB2 EPHB4 FUS FYN GRIN2A GRIN2B GRIN2D GRIN3A HNRNPU HRAS HSPA1A INA LNX1 LRP8 MAP2 MAP2K2 MYH9 NANOS1 NEFL NF1 PLAT PLCG1 PPP2R1A PPP2R2A PRKCA PRKCB PRKCE PRKCG RAP2A RPS6KA3 SP3 SPTAN1 SYNGAP1 TJP1 TRAF3 TUBA4B 13 interactors: CAMK2A DLG3 DLG4 DLGAP4 GRIN1 GRIN2B GRIN2D KDR MPDZ PDGFRB TRIP6 ULK1 ULK2
Entrez ID 2902 8831
HPRD ID 15926 16018
Ensembl ID ENSG00000176884 ENSG00000197283
Uniprot IDs Q05586 Q59GW0 Q5VSF9 Q96PV0
PDB IDs 2HQW 2NR1 3BYA
Enriched GO Terms of Interacting Partners?
Tagcloud ?
asah1  atypical  broadening  canada  care4rare  causal  definitive  descriptions  encephalopathy  epilepsy  exome  families  folr1  forge  grin2a  kcnq2  nation  projects  rare  recognizable  retrospect  scn8a  segregating  seizures  suited  synj1  translating  unrevealing  wes 
Tagcloud (Difference) ?
asah1  atypical  broadening  canada  care4rare  causal  definitive  descriptions  encephalopathy  epilepsy  exome  families  folr1  forge  grin2a  kcnq2  nation  projects  rare  recognizable  retrospect  scn8a  segregating  seizures  suited  synj1  translating  unrevealing  wes 
Tagcloud (Intersection) ?