ATN1 and RBFOX1

  • Number of citations of the paper that reports this interaction (PMID 16713569)
  • 214
  • Data Source:
  • BioGRID (affinity chromatography technology)
  • HPRD (two hybrid)

ATN1

RBFOX1

Gene Name atrophin 1 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 93 interactors: AES AGRN ALG13 ARF3 ATRX BAG6 BAIAP2 CACNB1 CASP1 CASP3 CBFA2T2 CENPJ CHRD CRACR2A CRIP2 CTNND2 DMPK DVL1 DVL2 ECM1 EFEMP1 EFEMP2 EWSR1 FBLN1 FBLN2 FBLN5 GAPDH GCC1 GIGYF1 GRN HINFP HSPG2 ITCH JAG2 KAT6A KAT6B KAT7 KRT31 KRTAP4-12 LENG8 LRP2 LTBP1 LTBP4 LYST MAGI1 MAGI2 MAP7D1 MBP MDFI MEGF11 MEGF6 MEGF8 NCK2 NELL1 NELL2 NOC2L NR2E1 PCSK5 PDCD6IP PFKL PLSCR1 PRRC2A PRRC2B PSMA3 PSME3 RAD54L2 RBFOX1 RBFOX2 RBM10 RBPMS RCHY1 RERE RHOXF2 RNF115 RNF31 RUNX1T1 SIAH1 SIAH2 SLIT1 SPAG5 SSPO STXBP4 SYVN1 TEP1 TLE1 TRIP6 USP54 VIM WDR5 WWP1 WWP2 ZMYND8 ZSWIM8 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 1822 54715
HPRD ID 06311 16091
Ensembl ID ENSG00000111676 ENSG00000078328
Uniprot IDs P54259 Q86V38 B7Z1U7 F5H0M1 Q59HD3 Q9NWB1
PDB IDs 2ERR
Enriched GO Terms of Interacting Partners?
Tagcloud ?
atrophin1  atrophy  chip  cortical  degenerative  demethylase  dentatorubral  depletion  h3k4  hint  inducing  knockout  lbal  lsd1  lysine  maintenance  methylation  npc  pallidoluysian  phenocopied  poorly  precise  premature  progenitor  repression  rescued  seq  surprisingly  tranylcypromine 
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) ?
atrophin1  atrophy  chip  cortical  degenerative  demethylase  dentatorubral  depletion  h3k4  hint  inducing  knockout  lbal  lsd1  lysine  maintenance  methylation  npc  pallidoluysian  phenocopied  poorly  precise  premature  progenitor  repression  rescued  seq  surprisingly  tranylcypromine 
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) ?