HNRNPR and SMN1

  • Number of citations of the paper that reports this interaction (PMID 11773003)
  • 58
  • Data Source:
  • HPRD (in vivo, in vitro)

HNRNPR

SMN1

Gene Name heterogeneous nuclear ribonucleoprotein R survival of motor neuron 1, telomeric
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 9 interactors: BMPR2 FARSA HIST3H3 IL7R KHDRBS2 PRMT1 RPL26 SMN1 TAB1 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
Entrez ID 10236 6606
HPRD ID 06228 02646
Ensembl ID ENSG00000125944 ENSG00000172062
Uniprot IDs B4DT28 E7ETM7 O43390 Q0VGD6 Q6MZS5 S4R3J4 B4DP61 Q16637
PDB IDs 2DK2 1G5V 1MHN 2LEH 3S6N 4A4E 4A4G 4GLI
Enriched GO Terms of Interacting Partners?
Tagcloud ?
absent  alleles  aml  atlas  australasian  bank  box  conjunction  enrichment  epigenetic  frequently  hypermethylation  leukemic  marks  matr3  promoter  sf3a1  sf3b1  silence  silico  somatic  splicing  srsf2  suppressing  u2af1  u937  ybx3  zfr  zrsr2 
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 
Tagcloud (Difference) ?
absent  alleles  aml  atlas  australasian  bank  box  conjunction  enrichment  epigenetic  frequently  hypermethylation  leukemic  marks  matr3  promoter  sf3a1  sf3b1  silence  silico  somatic  splicing  srsf2  suppressing  u2af1  u937  ybx3  zfr  zrsr2 
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 
Tagcloud (Intersection) ?