SMN1 and DOCK7

  • Number of citations of the paper that reports this interaction (PMID 21900206)
  • 27
  • Data Source:
  • BioGRID (two hybrid)

SMN1

DOCK7

Gene Name survival of motor neuron 1, telomeric dedicator of cytokinesis 7
Image No pdb structure
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 13 interactors: ANXA7 BCL2L1 CDC42 CDKN1A GRB7 PPP2CB RHOA RPP14 SMN1 SNCA TK1 WHSC1L1 YWHAG
Entrez ID 6606 85440
HPRD ID 02646 16833
Ensembl ID ENSG00000172062 ENSG00000116641
Uniprot IDs B4DP61 Q16637 Q96N67 Q96NI0
PDB IDs 1G5V 1MHN 2LEH 3S6N 4A4E 4A4G 4GLI
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 
2510dela  3709c  6232g  983c  abolish  arg1237  asp837alafs  blindness  dysmorphic  encephalopathies  epileptic  exome  gabaergic  genesis  glu2078  heterozygotes  hyperintensities  interneurons  intractable  nonconsanguineous  pontobulbar  proband  rac  sanger  ser328  sisters  sulcus  syndromic  truncating 
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 
2510dela  3709c  6232g  983c  abolish  arg1237  asp837alafs  blindness  dysmorphic  encephalopathies  epileptic  exome  gabaergic  genesis  glu2078  heterozygotes  hyperintensities  interneurons  intractable  nonconsanguineous  pontobulbar  proband  rac  sanger  ser328  sisters  sulcus  syndromic  truncating 
Tagcloud (Intersection) ?