CACNA1A and TSC22D1

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

CACNA1A

TSC22D1

Gene Name calcium channel, voltage-dependent, P/Q type, alpha 1A subunit TSC22 domain family, member 1
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Antineutrophil cytoplasmic antibody-associated vasculitis ( 22808956)
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 49 interactors: A2M APLP1 ASAH1 C14orf1 C9orf9 CACNA1A CARHSP1 CCDC90B CHD3 CORO2B CRMP1 DDAH2 DNMT3B EED FAF1 FAM20C FBN3 GNB2 GNB5 HMGXB4 KMT2B KMT2C LRIF1 MAP3K12 MCM3AP NCOA5 OTUB1 PDHB PRKCI PTN QARS RGS1 RPL5 SETDB1 SP110 SPRED1 TAF5L TGFBR1 TLE1 TP53 TSC22D4 UBE2D1 UNC119 VIM WDR73 WDYHV1 WIZ WNK1 ZC3HC1
Entrez ID 773 8848
HPRD ID 03004 07414
Ensembl ID ENSG00000141837
Uniprot IDs B5TYJ1 O00555 Q9NS89 A8K3Y6 Q15714
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 
beadchip  capn13  cards  cic  collect  conjunctival  cxcl6  cytology  drb5  dry  entire  eye  ht  illumina  impression  investigates  lysozyme  mini  optimally  optimization  psca  qiagen  qrt  qualifying  rneasy  severities  steps  taqman  transcriptome 
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 
beadchip  capn13  cards  cic  collect  conjunctival  cxcl6  cytology  drb5  dry  entire  eye  ht  illumina  impression  investigates  lysozyme  mini  optimally  optimization  psca  qiagen  qrt  qualifying  rneasy  severities  steps  taqman  transcriptome 
Tagcloud (Intersection) ?