SMN1 and HNRNPU

  • Number of citations of the paper that reports this interaction (PMID 8670859)
  • 146
  • Data Source:
  • HPRD (two hybrid, in vivo)

SMN1

HNRNPU

Gene Name survival of motor neuron 1, telomeric heterogeneous nuclear ribonucleoprotein U (scaffold attachment factor A)
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 136 interactors: A1BG A2M ACTB ACTL6B ADAMTS10 AGAP1 APLP1 ARFGAP1 ATP5B ATP6V1A BAG6 BCL2 C19orf60 CARHSP1 CCDC90B CENPB COIL COL4A2 COL4A5 COPS6 CPNE6 CRIP2 CSAD DDAH2 DDX20 DHX9 DMPK DOCK7 DUS2 DYNC1I1 EEF1A1 EIF3G EXT2 EZH2 FAM20C FBL FGB FLAD1 FUBP1 GAPDH GAR1 GDF9 GEMIN2 GEMIN5 GEMIN7 HADHB HIST3H3 HMGXB3 HNRNPR HNRNPU HNRNPUL1 IGHM ILF3 IMMT INPP5K JADE1 KDM1A KIF5A KLHL5 KMT2B KPNB1 LENG8 LRIF1 LSM1 LSM10 LSM11 LSM2 LSM3 LSM4 LSM5 LSM6 LSM7 MAST2 MED31 MKI67 MPP1 MRPL37 MSH2 NGFR NKIRAS2 NMT2 OSTF1 PDE4DIP PKM PLXNA3 POLR2A POP7 PSME1 QARS RBBP4 RBBP6 RBFOX2 RBM48 RN7SL1 RNU1-1 RNU2-1 RPL13 RPS2 RXRA SDF4 SEMA5B SETDB1 SMC5 SMN2 SNRPB SNRPD1 SNRPD2 SNRPD3 SNRPE SNUPN SP110 STRAP STXBP2 STXBP3 SULT1A3 SUMO3 SYNCRIP TAF1C TIAL1 TLE1 TMSB4X TP53 TRMT2A TUBA1A TUBB3 UCHL1 UNC119 USP4 WDR18 WDR73 WDYHV1 WIZ ZBTB16 ZNF431 ZRANB2 ZXDC 35 interactors: ACTB BTRC CASP3 CD5 CDKN2A CR2 ELL EP300 ERG GAS7 GRIN1 GRIN2D GTF2H1 HNRNPD HNRNPH3 IL7R KAT2B NDN NDRG1 NEDD4 NR3C1 PIN1 POLR2A POU3F4 PRMT1 PRPF40A PTPN11 SMN1 SREK1 STAU1 SYK TCERG1 WBP4 YAP1 ZNF689
Entrez ID 6606 3192
HPRD ID 02646 04185
Ensembl ID ENSG00000172062 ENSG00000153187
Uniprot IDs B4DP61 Q16637 Q00839 Q96BA7
PDB IDs 1G5V 1MHN 2LEH 3S6N 4A4E 4A4G 4GLI 1ZRJ
Enriched GO Terms of Interacting Partners?
Tagcloud ?
atrophy  centromeric  compensate  copies  copy  degeneration  deletions  detectable  display  donor  easily  exon  fails  fatal  harbor  hindering  homozygous  infant  intragenic  italian  modifier  muscular  null  predictable  sma  smn2  splice  unusually  weakness 
17p13  1q21  1q44  2q23  2q31  agilent  annotations  asd  autism  backgrounds  cgh  cnv  cnvs  disabilities  dissect  encephalopathy  epileptic  exome  expand  hallux  implicates  infantile  intellectual  lissencephaly  mbd5  microcephaly  pafah1b1  pathogenicity  spasms 
Tagcloud (Difference) ?
atrophy  centromeric  compensate  copies  copy  degeneration  deletions  detectable  display  donor  easily  exon  fails  fatal  harbor  hindering  homozygous  infant  intragenic  italian  modifier  muscular  null  predictable  sma  smn2  splice  unusually  weakness 
17p13  1q21  1q44  2q23  2q31  agilent  annotations  asd  autism  backgrounds  cgh  cnv  cnvs  disabilities  dissect  encephalopathy  epileptic  exome  expand  hallux  implicates  infantile  intellectual  lissencephaly  mbd5  microcephaly  pafah1b1  pathogenicity  spasms 
Tagcloud (Intersection) ?