FANCA and TCERG1

  • Number of citations of the paper that reports this interaction (PMID 14499622)
  • 5
  • Data Source:
  • BioGRID (two hybrid)

FANCA

TCERG1

Gene Name Fanconi anemia, complementation group A transcription elongation regulator 1
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 46 interactors: AKT1 ALDOA ATP5B ATR AZIN1 BRCA1 CAPN1 CCT3 CD79A CDK1 CENPE DAXX DDX39B DNAJB1 DUS4L ENO1 FANCC FANCE FANCF FANCG GNB2 HES1 HPRT1 HSP90AA1 IFIT3 IKBKB KRT1 LIPG MKNK1 MX1 NAMPT NUB1 PRPF31 PSMA5 RPL18 SGK1 SMARCA4 SMARCC1 SMARCD3 SNX5 SPTAN1 TAF10 TCERG1 TCP1 TPT1 ZNF24 52 interactors: ABI1 BARD1 BRD4 CHAF1A CHD3 CPSF6 CYFIP1 CYFIP2 DIAPH1 DIAPH2 DNAJB9 EVL FANCA FANCC FMNL1 GRB2 HNRNPH1 HNRNPK HNRNPM HNRNPU HSPA1A HSPA5 HSPA8 HTT JUNB LUC7L NONO NPM1 NUDT21 PCBP1 PIAS4 POLR2A PSPC1 SETDB1 SF1 SF3A1 SF3A2 SF3A3 SF3B1 SF3B2 SF3B3 SF3B4 SFPQ SRSF1 SUMO1 TPM4 U2AF2 WAS WASF2 WBP4 WIPF2 WWOX
Entrez ID 2175 10915
HPRD ID 06186 10393
Ensembl ID ENSG00000187741 ENSG00000113649
Uniprot IDs H3BSR5 O15360 Q86U55 O14776
PDB IDs 2DK7 2DOD 2DOE 2DOF 2E71 2KIQ 2KIS 2NNT 3HFH 4FQG
Enriched GO Terms of Interacting Partners?
Tagcloud ?
aml  anemia  aplastic  autosomal  brca2  collaborate  complicated  cumulative  cure  decision  fancd1  fanconi  fancq  genotypes  gynecologic  head  inherited  neck  preemptive  prone  recessive  risks  solid  squamous  subset  transplant  usually  wilms 
12p13  12q21  17q11  3q26  5q22  5q32  acgh  bac  balanced  ccnd2  clonality  cnas  concordant  cryptic  cytogenetics  emp1  evi1  evolving  exploratory  hidden  imbalances  karyotypically  karyotyping  kitlg  nf1  platforms  recurring  submicroscopic  unidentified 
Tagcloud (Difference) ?
aml  anemia  aplastic  autosomal  brca2  collaborate  complicated  cumulative  cure  decision  fancd1  fanconi  fancq  genotypes  gynecologic  head  inherited  neck  preemptive  prone  recessive  risks  solid  squamous  subset  transplant  usually  wilms 
12p13  12q21  17q11  3q26  5q22  5q32  acgh  bac  balanced  ccnd2  clonality  cnas  concordant  cryptic  cytogenetics  emp1  evi1  evolving  exploratory  hidden  imbalances  karyotypically  karyotyping  kitlg  nf1  platforms  recurring  submicroscopic  unidentified 
Tagcloud (Intersection) ?