TTN and FLNA

  • Number of citations of the paper that reports this interaction (PMID 16902413)
  • 53
  • Data Source:
  • HPRD (two hybrid)

TTN

FLNA

Gene Name titin filamin A, alpha
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 29 interactors: ACTA1 ACTN1 ACTN2 ANK1 ANKRD1 ANKRD2 ANKRD23 CALM1 CAPN3 CRYAB FHL1 FHL2 FLNA MAPK1 MYBPC1 MYBPC3 MYH9 MYOM1 MYOM2 MYPN NBR1 NEB OBSCN SQSTM1 SRPK2 TCAP TRIM55 TRIM63 VAV2 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 7273 2316
HPRD ID 01787 02060
Ensembl ID ENSG00000155657 ENSG00000196924
Uniprot IDs Q7Z3B7 Q8WZ42 P21333 Q60FE5 Q6NXF2
PDB IDs 1BPV 1G1C 1NCT 1NCU 1TIT 1TIU 1TKI 1TNM 1TNN 1WAA 1YA5 2A38 2BK8 2F8V 2ILL 2J8H 2J8O 2NZI 2RQ8 2WP3 2WWK 2WWM 2Y9R 3B43 3KNB 3LCY 3LPW 3PUC 3Q5O 3QP3 2AAV 2BP3 2BRQ 2J3S 2JF1 2K3T 2K7P 2K7Q 2W0P 2WFN 3CNK 3HOC 3HOP 3HOR 3ISW 3RGH
Enriched GO Terms of Interacting Partners?
Tagcloud ?
amounts  anticancer  atlas  braf  broad  diverse  exome  frequencies  frequency  frg1b  harbored  includes  integrated  lineage  metastastic  muc16  mutated  mutational  obtain  omics  pbrm1  resource  sequencing  somatic  subtypes  summarized  ush2a  varied  vhl 
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) ?
amounts  anticancer  atlas  braf  broad  diverse  exome  frequencies  frequency  frg1b  harbored  includes  integrated  lineage  metastastic  muc16  mutated  mutational  obtain  omics  pbrm1  resource  sequencing  somatic  subtypes  summarized  ush2a  varied  vhl 
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) ?