KALRN and CACNA1A

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

KALRN

CACNA1A

Gene Name kalirin, RhoGEF kinase calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 15 interactors: ATXN7 CACNA1A CDC5L COIL DISC1 DTNBP1 EPHB2 FASLG GFI1B LNX1 NDEL1 PAM RAC1 SUMO2 SUMO3 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 8997 773
HPRD ID 06859 03004
Ensembl ID ENSG00000160145 ENSG00000141837
Uniprot IDs J3QSW6 O60229 B5TYJ1 O00555 Q9NS89
PDB IDs 3BXK
Enriched GO Terms of Interacting Partners?
Tagcloud ?
actionable  adamts18  col1a1  d816  dgki  epha4  epha7  g12  g13  gna11  gnaq  gucy2c  k642  l576  melanomas  mined  ngs  nras  pik3r4  ppp6c  prkaa2  q209  q61  stk31  taf1l  trpm6  v559  v600  w557 
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) ?
actionable  adamts18  col1a1  d816  dgki  epha4  epha7  g12  g13  gna11  gnaq  gucy2c  k642  l576  melanomas  mined  ngs  nras  pik3r4  ppp6c  prkaa2  q209  q61  stk31  taf1l  trpm6  v559  v600  w557 
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 (Intersection) ?