DOCK7 and WHSC1L1

  • Number of citations of the paper that reports this interaction (PMID 23455924)
  • 3
  • Data Source:
  • BioGRID (two hybrid)

DOCK7

WHSC1L1

Gene Name dedicator of cytokinesis 7 Wolf-Hirschhorn syndrome candidate 1-like 1
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 13 interactors: ANXA7 BCL2L1 CDC42 CDKN1A GRB7 PPP2CB RHOA RPP14 SMN1 SNCA TK1 WHSC1L1 YWHAG 17 interactors: CBX3 CBX5 DAXX DOCK7 ETV3 GLYR1 H3F3C HIST1H1A HOXC4 MLLT6 MNDA SEPT6 SLU7 SPAG8 STAC3 UBE2I ZNF557
Entrez ID 85440 54904
HPRD ID 16833 06155
Ensembl ID ENSG00000116641 ENSG00000147548
Uniprot IDs Q96N67 Q96NI0 B7ZL11 Q9BZ95
PDB IDs 2DAQ 4GND 4GNE 4GNF 4GNG
Enriched GO Terms of Interacting Partners?
Tagcloud ?
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 
aside  c5hch  cys  dimethylase  fifth  h3k36  h3k4  h3k9  h3k9me0  h3k9me3  homeodomain  k9  k9me3  methyltransferases  mmset  module  mono  nonredundant  nsd  nsd1  nsd2  nsd3  phd  phd5  shed  trimethylated  unmethylated  unmodified 
Tagcloud (Difference) ?
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 
aside  c5hch  cys  dimethylase  fifth  h3k36  h3k4  h3k9  h3k9me0  h3k9me3  homeodomain  k9  k9me3  methyltransferases  mmset  module  mono  nonredundant  nsd  nsd1  nsd2  nsd3  phd  phd5  shed  trimethylated  unmethylated  unmodified 
Tagcloud (Intersection) ?