SLC22A5 and SLC9A3R2

  • Number of citations of the paper that reports this interaction (PMID 15553237)
  • 5
  • Data Source:
  • HPRD (two hybrid)

SLC22A5

SLC9A3R2

Gene Name solute carrier family 22 (organic cation/carnitine transporter), member 5 solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 2
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 4 interactors: PDZD3 PDZK1 SLC9A3R1 SLC9A3R2 35 interactors: ABCC4 ACTN4 ADORA2B ADRB2 ATP2B2 CFTR EZR KCNJ1 LPAR1 LPAR2 P2RY1 PDPK1 PDZK1 PIK3CA PLCB3 PODXL PRKACA PTEN PTH1R RDX SGK1 SGK3 SIAH1 SLC22A4 SLC22A5 SLC22A9 SLC26A3 SLC34A1 SLC9A3 SLCO1A2 SLCO3A1 SRY TAZ TBC1D10A WWTR1
Entrez ID 6584 9351
HPRD ID 04539 05946
Ensembl ID ENSG00000197375 ENSG00000065054
Uniprot IDs O76082 Q15599
PDB IDs 2D11 2HE4 2OCS
Enriched GO Terms of Interacting Partners?
Tagcloud ?
abstracted  alleles  c113y  cardiomyopathy  carnitine  compound  confirm  corresponding  deficiency  detect  frequently  genomic  heterozygous  homozygous  missense  mutated  mutation  mutations  nonsense  parents  pcd  polyphen  predict  r254x  r289x  sanger  sequencing  sift  throughput 
Tagcloud (Difference) ?
abstracted  alleles  c113y  cardiomyopathy  carnitine  compound  confirm  corresponding  deficiency  detect  frequently  genomic  heterozygous  homozygous  missense  mutated  mutation  mutations  nonsense  parents  pcd  polyphen  predict  r254x  r289x  sanger  sequencing  sift  throughput 
Tagcloud (Intersection) ?