NMNAT1 and KPNA2

  • Number of citations of the paper that reports this interaction (PMID 25416956)
  • 0
  • Data Source:
  • BioGRID (two hybrid)

NMNAT1

KPNA2

Gene Name nicotinamide nucleotide adenylyltransferase 1 karyopherin alpha 2 (RAG cohort 1, importin alpha 1)
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 10 interactors: APP CCNC FLOT2 KPNA2 MSX1 NEK3 NTRK2 SIK1 SIRT1 TDO2 104 interactors: ACTN1 ACTN4 ANKIB1 AP2B1 APOBEC1 APP ARL4A ARL5A BRCA1 BTBD2 CASP2 CCDC107 CDA CDK5RAP3 CHD3 CHEK2 CORO1B CREB3L3 CREBBP CSE1L CSNK1A1 CUL4B DCTN2 DDIT3 EP300 EPB41 FEZ2 FN1 FTH1 GART GMCL1 GRB2 H1F0 HAP1 HMG20A HNRNPC HOMER2 HOMEZ HSPA4 IFT20 IMMT INO80E ITK JUN KLC4 KPNB1 KRT18 KRT40 KRT8 LAMB2 LEF1 LZTS2 MAGED1 MAGEH1 MDFI MLH1 MORC3 MVP MYC NECAB2 NFKBIB NMNAT1 NR3C1 NUP153 NUP50 NUP62 NUTM1 PAX5 PLAG1 PNMA5 PRKD3 PTMA RAG1 RAN RANBP2 RBM48 RBPMS RECQL RELA RELB RGL2 RILP RNMT SART3 SERTAD3 SGK1 SLC2A2 SPRY1 SRPK1 TADA2A TAF3 TAF8 TANK TBPL2 TP53 TRAF1 TRIM54 TSC22D4 TXNIP UBR5 USHBP1 ZBTB7B ZC3H12A ZNF131
Entrez ID 64802 3838
HPRD ID 16369 02818
Ensembl ID ENSG00000173614 ENSG00000182481
Uniprot IDs B1AN62 Q9HAN9 P52292 Q7Z726
PDB IDs 1GZU 1KKU 1KQN 1KQO 1KR2 1EFX 1QGK 1QGR 3FEX 3FEY 4E4V
Enriched GO Terms of Interacting Partners?
Tagcloud ?
adenylyltransferase  amaurosis  atrophy  autosomal  caucasian  cone  crd  dystrophies  dystrophy  e257k  encompassed  harbors  heterozygous  inherited  insignificant  lca  leber  macular  modifier  nicotinamide  persons  pigmentosa  recessive  retinitis  rod  rp  sanger  truncating  variants 
aggressive  aggressiveness  assembled  attempt  carcinomas  curable  diagnostics  disregarding  eic  emgd  endometrial  entities  figo  immunoreactivity  interplay  introducing  malignancy  mediator  mfe  microarrays  nucleocytoplasmic  precancerous  regimens  surgically  tmas  trp53  tumour  untreatable  uterus 
Tagcloud (Difference) ?
adenylyltransferase  amaurosis  atrophy  autosomal  caucasian  cone  crd  dystrophies  dystrophy  e257k  encompassed  harbors  heterozygous  inherited  insignificant  lca  leber  macular  modifier  nicotinamide  persons  pigmentosa  recessive  retinitis  rod  rp  sanger  truncating  variants 
aggressive  aggressiveness  assembled  attempt  carcinomas  curable  diagnostics  disregarding  eic  emgd  endometrial  entities  figo  immunoreactivity  interplay  introducing  malignancy  mediator  mfe  microarrays  nucleocytoplasmic  precancerous  regimens  surgically  tmas  trp53  tumour  untreatable  uterus 
Tagcloud (Intersection) ?