CACNB4 and CACNA1A

  • Number of citations of the paper that reports this interaction (PMID 9442082)
  • 40
  • Data Source:
  • HPRD (in vitro)

CACNB4

CACNA1A

Gene Name calcium channel, voltage-dependent, beta 4 subunit calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 9 interactors: CACNA1A CBX3 FASLG MAP1A MED31 PTN REM1 SYT1 TBL3 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
Entrez ID 785 773
HPRD ID 09057 03004
Ensembl ID ENSG00000182389 ENSG00000141837
Uniprot IDs E7DBM8 O00305 B5TYJ1 O00555 Q9NS89
PDB IDs 1VYV 2D46 3BXK
Enriched GO Terms of Interacting Partners?
Tagcloud ?
altering  concomitantly  couples  dephosphorylation  electrical  epilepsy  excitability  gated  gk  guanylate  hp1gamma  hydroxylase  juvenile  modules  myoclonic  platform  pp2a  ppp2r5  ppp2r5d  prevents  r482x  recruiting  repressor  sh3  signalling  th  tralpha  vgcc  voltage 
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 
Tagcloud (Difference) ?
altering  concomitantly  couples  dephosphorylation  electrical  epilepsy  excitability  gk  guanylate  hp1gamma  hydroxylase  juvenile  modules  myoclonic  platform  pp2a  ppp2r5  ppp2r5d  prevents  r482x  recruiting  repressor  sh3  signalling  th  tralpha  vgcc 
acetazolamide  ataxia  attacks  autosomal  causative  causing  coincidence  confutes  defect  dysarthria  dystonia  ea  ea2  encodes  episodes  episodic  gait  heterogeneous  inherited  migraine  mim  nonsense  oculomotor  paroxysmal  q  varied 
Tagcloud (Intersection) ?
gated  voltage