CACNA1A and TAF15

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

CACNA1A

TAF15

Gene Name calcium channel, voltage-dependent, P/Q type, alpha 1A subunit TAF15 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 68kDa
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
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 21 interactors: CACNA1A FUS HIST1H3A HIST2H2AC HIST2H4A HIST3H3 POLR2C POLR2E POLR2G PRMT1 PRMT8 SAFB SF1 TAF1 TAF12 TAF13 TAF5 TAF7 TBP YWHAG ZNF384
Entrez ID 773 8148
HPRD ID 03004 09031
Ensembl ID ENSG00000141837 ENSG00000172660
Uniprot IDs B5TYJ1 O00555 Q9NS89 Q86X94 Q92804
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 
amyotrophic  autosomal  carriers  coding  conserved  equivocal  et  ewsr1  exons  export  familial  frontotemporal  fus  genotyped  genotyping  hnrnpa1  hnrnpa2b1  lobar  nes  neurodegeneration  pathogenicity  r471c  relatives  sequenced  subject  substitution  tardbp  tdp43  tremor 
Tagcloud (Difference) ?
acetazolamide  ataxia  attacks  causative  causing  coincidence  confutes  defect  dysarthria  dystonia  ea  ea2  encodes  episodes  episodic  gait  gated  heterogeneous  inherited  migraine  mim  nonsense  oculomotor  paroxysmal  q  varied  voltage 
amyotrophic  carriers  coding  conserved  equivocal  et  ewsr1  exons  export  familial  frontotemporal  fus  genotyped  genotyping  hnrnpa1  hnrnpa2b1  lobar  nes  neurodegeneration  pathogenicity  r471c  relatives  sequenced  subject  substitution  tardbp  tdp43  tremor 
Tagcloud (Intersection) ?
autosomal