DNAJB5 and CACNA1A

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

DNAJB5

CACNA1A

Gene Name DnaJ (Hsp40) homolog, subfamily B, member 5 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 2 interactors: CACNA1A TBPL2 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 25822 773
HPRD ID 07106 03004
Ensembl ID ENSG00000137094 ENSG00000141837
Uniprot IDs O75953 B5TYJ1 O00555 Q9NS89
PDB IDs 3BXK
Enriched GO Terms of Interacting Partners?
Tagcloud ?
1a  applicable  biopsy  bowel  cd  cohorts  colitis  crohn  enabled  examining  hnmt  homologue  hsp40  ibd  inflamed  influencing  intestinal  junb  microarray  nc  ppbp  proplatelet  step  subfamily  subforms  suffering  uc  ulcerative  uses 
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) ?
applicable  biopsy  bowel  cd  cohorts  colitis  crohn  enabled  examining  hnmt  homologue  hsp40  ibd  inflamed  influencing  intestinal  junb  microarray  nc  ppbp  proplatelet  step  subfamily  subforms  suffering  uc  ulcerative  uses 
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) ?
1a