CACNA1A and FBLN1

  • Number of citations of the paper that reports this interaction (PMID 21078624)
  • 14
  • Data Source:
  • BioGRID (two hybrid)

CACNA1A

FBLN1

Gene Name calcium channel, voltage-dependent, P/Q type, alpha 1A subunit fibulin 1
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Temperament (bipolar disorder) ( 22365631)
Protein-Protein Interactions 92 interactors: ABCA2 ABI1 ACTN1 AGRN ALDOA AMIGO2 AP2M1 ARHGAP22 ASNA1 BTG3 BZRAP1 C1QTNF1 CABP1 CACNB1 CACNB4 CALM2 CALM3 CKAP5 CRIM1 CRMP1 CSNK2B CYSRT1 DNAJB5 EFEMP1 EFEMP2 EHMT2 EIF3A FBLN1 GNB1 GOLGA6L5P GRN HECW1 HHATL HIVEP1 HSPG2 IP6K1 JAG2 KALRN KHDRBS3 KIAA1191 LAMB1 LLGL1 LPHN1 LRP1 LTBP1 LTBP3 LTBP4 MANBAL MATK MATN2 MEGF6 MEGF8 MIA3 MOAP1 NDUFB8 NELFCD NELL1 NELL2 NOTCH1 NOXA1 OLIG1 PCSK5 PCSK6 PMM1 PPIG PPM1A PPP1R12C PTGDS PUF60 RBM12B RIMBP2 RPL31 RPS17 SCP2 SPRY1 SRRM4 SRSF1 SUMF2 SYT1 TAF15 TELO2 TSC22D1 TSPAN7 TUBB2B UQCRC2 VARS VPS52 VWF WBP1 YLPM1 ZCCHC17 ZNF233 35 interactors: ACAN ADAMTSL2 ADAMTSL4 APOA1 APP ATN1 BHLHE40 CACNA1A CTGF ECM1 EDC4 ELN FGB FN1 GFI1B HBEGF HSPG2 ITGB1 LTBP4 MFAP5 MOB4 NEDD1 NID1 NOTCH3 NOV PLSCR1 SKIL SMAD3 SMAD4 TAF9 TANK TCF7L2 TDGF1 VCAN YWHAQ
Entrez ID 773 2192
HPRD ID 03004 00629
Ensembl ID ENSG00000141837 ENSG00000077942
Uniprot IDs B5TYJ1 O00555 Q9NS89 P23142 Q8NBH6
PDB IDs 3BXK
Enriched GO Terms of Interacting Partners?
Tagcloud ?
acetazolamide  ataxia  attacks  autosomal  causative  causing  coincidence  confutes  defect  dysarthria  dystonia  ea  ea2  encodes  episodes  episodic  gait  gated  heterogeneous  inherited  migraine  mim  nonsense  oculomotor  paroxysmal  q  varied  voltage 
3t3  alters  anchorage  arntl2  bfsp2  bmp7  celsr1  confocal  deregulated  etv5  exhibits  filopodia  fmn2  gfra2  gpm6a  gpm6b  graffi  homologs  malignancies  mulv  nih  nln  oligonucleotide  oncogenes  parm  peri  protrusions  punctate  semi 
Tagcloud (Difference) ?
acetazolamide  ataxia  attacks  autosomal  causative  causing  coincidence  confutes  defect  dysarthria  dystonia  ea  ea2  encodes  episodes  episodic  gait  gated  heterogeneous  inherited  migraine  mim  nonsense  oculomotor  paroxysmal  q  varied  voltage 
3t3  alters  anchorage  arntl2  bfsp2  bmp7  celsr1  confocal  deregulated  etv5  exhibits  filopodia  fmn2  gfra2  gpm6a  gpm6b  graffi  homologs  malignancies  mulv  nih  nln  oligonucleotide  oncogenes  parm  peri  protrusions  punctate  semi 
Tagcloud (Intersection) ?