CACNA1A and TUBB2B

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

CACNA1A

TUBB2B

Gene Name calcium channel, voltage-dependent, P/Q type, alpha 1A subunit tubulin, beta 2B class IIb
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 10 interactors: ANXA7 BID C8orf33 CACNA1A CDKN1A CENPU CSNK2B HDAC6 RGS2 RPL35
Entrez ID 773 347733
HPRD ID 03004 14707
Ensembl ID ENSG00000141837 ENSG00000137285
Uniprot IDs B5TYJ1 O00555 Q9NS89 Q9BVA1
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 
200x  customized  dcx  depths  dync1h1  exome  flna  funded  heterotopia  kif5c  kinesin  malformations  megalencephaly  mosaicism  neurodevelopmental  neuropsychiatric  nodular  pachygyria  panels  periventricular  persons  polymicrogyria  read  sanger  somatic  subcloned  subcloning  subcortical  unequal 
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 
200x  customized  dcx  depths  dync1h1  exome  flna  funded  heterotopia  kif5c  kinesin  malformations  megalencephaly  mosaicism  neurodevelopmental  neuropsychiatric  nodular  pachygyria  panels  periventricular  persons  polymicrogyria  read  sanger  somatic  subcloned  subcloning  subcortical  unequal 
Tagcloud (Intersection) ?