DAB1 and RBFOX1

  • Number of citations of the paper that reports this interaction (PMID 24722188)
  • 1
  • Data Source:
  • BioGRID (two hybrid)

DAB1

RBFOX1

Gene Name Dab, reelin signal transducer, homolog 1 (Drosophila) RNA binding protein, fox-1 homolog (C. elegans) 1
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 73 interactors: APLP1 APLP2 APP ARID5A BHLHE40 C1orf94 CDK5 CDK6 CIART CLASRP CRK CRKL DAB2IP DAZAP2 ERBB2 ERBB3 FAM103A1 FAM168A HMBOX1 HNRNPLL HYAL3 INPP5D ITGB2 ITGB3 ITGB5 ITGB7 KRTAP19-5 KRTAP19-7 KRTAP8-1 LDLR LGALS9B LGALS9C LNX1 LRP1 LRP2 LRP8 MAGED1 MBNL1 MBNL3 MYO6 NAF1 PAFAH1B1 PCDH18 PIN1 PLCG1 POGZ PPIG PRR20A PTPN11 RBFOX1 RBFOX2 RELN RHOXF2 ROR2 SERF2 SIAH1 SIRPB1 SMAP2 SNRPB SRC STRBP TCEA2 TCEANC TMTC3 TOLLIP USP53 VENTX VLDLR WDYHV1 ZBTB32 ZC3H10 ZCCHC10 ZNF488 33 interactors: ALG13 ATN1 ATXN1 ATXN2 BHLHE40 C1orf94 CELF3 CRX DAB1 DAZAP2 DMRTB1 DVL2 FAM168A GCA HNRNPF HSFX1 HSFY1 KIFAP3 LZTS2 MAGED1 NOC2L NUMBL PCBP4 PRR20A PRRC2A PSMF1 QKI RBFOX2 RBM24 RBPMS RHOXF2 SNRPN TNIP1
Entrez ID 1600 54715
HPRD ID 04582 16091
Ensembl ID ENSG00000173406 ENSG00000078328
Uniprot IDs O75553 B7Z1U7 F5H0M1 Q59HD3 Q9NWB1
PDB IDs 2ERR
Enriched GO Terms of Interacting Partners?
Tagcloud ?
assist  cajal  connections  cortical  d1x  dieker  disabled  doublecortn  dubbed  dysplasias  hydrolase  instructs  lis1  lissencephaly  malformation  marginal  miller  neuregulin  neurotrophic  neurotrophin  p35  plate  preplate  radial  reelin  retzius  tangential  tbr  thalamocortical 
16p13  2p13  3p13  abat  anomalies  cgh  cytogenetic  determining  difficulties  disability  duplicated  duplication  duplications  dysmorphisms  epilepsy  facial  girl  grin2a  hotspot  intellectual  litaf  microdeletions  novo  omim  overlapping  pmm2  spanning  tmem114  vertebral 
Tagcloud (Difference) ?
assist  cajal  connections  cortical  d1x  dieker  disabled  doublecortn  dubbed  dysplasias  hydrolase  instructs  lis1  lissencephaly  malformation  marginal  miller  neuregulin  neurotrophic  neurotrophin  p35  plate  preplate  radial  reelin  retzius  tangential  tbr  thalamocortical 
16p13  2p13  3p13  abat  anomalies  cgh  cytogenetic  determining  difficulties  disability  duplicated  duplication  duplications  dysmorphisms  epilepsy  facial  girl  grin2a  hotspot  intellectual  litaf  microdeletions  novo  omim  overlapping  pmm2  spanning  tmem114  vertebral 
Tagcloud (Intersection) ?