SLC9A3R1 and SLC22A5

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

SLC9A3R1

SLC22A5

Gene Name solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1 solute carrier family 22 (organic cation/carnitine transporter), member 5
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 52 interactors: ABCC2 ABCC4 ADRB2 AKAP10 ATP6V1B1 ATP6V1E1 BCL10 CFTR CLCN3 CNGA2 CTNNB1 EGFR EZR GNA11 GNAQ GRK6 KCNJ1 LHCGR LPAR2 MSN NF2 NOS2 OPRK1 P2RY1 PAG1 PDGFRA PDGFRB PDZK1 PIK3CA PLCB1 PLCB2 PTEN PTH1R RDX RLBP1 SCN4A SLC22A11 SLC22A4 SLC22A5 SLC22A9 SLC26A3 SLC34A1 SLC4A8 SLC9A3 SLCO1A2 SLCO3A1 TBC1D10A TRPC4 TRPC5 YAP1 YES1 ZNF468 4 interactors: PDZD3 PDZK1 SLC9A3R1 SLC9A3R2
Entrez ID 9368 6584
HPRD ID 05406 04539
Ensembl ID ENSG00000109062 ENSG00000197375
Uniprot IDs O14745 O76082
PDB IDs 1G9O 1GQ4 1GQ5 1I92 1SGH 2D10 2JXO 2KJD 2KRG 2M0T 2M0U 2M0V 2OZF
Enriched GO Terms of Interacting Partners?
Tagcloud ?
adipogenic  alters  amscs  chondrogenic  commitment  deacetylases  destabilizes  foxo1  grown  hdac  hdac1  hdac11  hydroxamic  hyper  interferes  lysate  manipulation  mechanistically  mesenchymal  multipotency  multipotent  nherf1  osteogenic  perturbation  pluripotent  saha  sirt7  suberoylanilide  uncommitted 
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) ?
adipogenic  alters  amscs  chondrogenic  commitment  deacetylases  destabilizes  foxo1  grown  hdac  hdac1  hdac11  hydroxamic  hyper  interferes  lysate  manipulation  mechanistically  mesenchymal  multipotency  multipotent  nherf1  osteogenic  perturbation  pluripotent  saha  sirt7  suberoylanilide  uncommitted 
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) ?