KRT20 and FXR2

  • Number of citations of the paper that reports this interaction (PMID 16189514)
  • 699

KRT20

FXR2

Gene Name keratin 20, type I fragile X mental retardation, autosomal homolog 2
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 27 interactors: ABI2 AMOTL2 ANKRD36BP1 C9orf16 CCDC85B COASY EIF4E2 EXOC8 FXR2 KRT13 KRT15 KRT40 KRT80 KRTAP10-7 KRTAP10-8 KRTAP10-9 NOTCH2NL NUP62 PIK3R2 PLEKHA5 PRC1 TFIP11 TXLNA USHBP1 VIM ZC2HC1C ZC3H14 90 interactors: AMOTL2 AP1M1 AP2M1 ARL6IP1 BAZ2B BRCA1 BYSL C10orf62 C1orf35 CALCOCO2 CAMK2D CBS CCDC33 CCDC85B CDKL3 CEP44 CEP55 COIL CYFIP1 CYFIP2 DPPA2 EWSR1 FAM90A1 FBP1 FMR1 FTH1 FXR1 GKAP1 HMBOX1 HNRNPC KCNRG KCTD4 KIAA1217 KIF1A KRT20 KXD1 LASP1 LCMT1 LCP2 LDOC1 MBIP MCRS1 MEAF6 MFAP1 MIA3 MORF4L1 MRPL43 NCK2 NDN NECAB2 NIF3L1 NME1 NONO NT5C2 PAF1 PAICS PCBD1 PIM1 POM121 PRAM1 PSME3 PTS RABAC1 RALYL RBBP8 RBMX RBPMS RPIA RTN3 RTN4 SCEL SNAP23 SRPK2 SSSCA1 SYT6 SYTL4 TBC1D22B THAP1 TNNT1 TRAF2 TRIM23 TRIM29 TRIM37 TSC22D4 YES1 ZBTB22 ZBTB8A ZMAT2 ZNF451 ZSCAN1
Entrez ID 54474 9513
HPRD ID 12193 05629
Ensembl ID ENSG00000171431 ENSG00000129245
Uniprot IDs P35900 P51116
PDB IDs 3H8Z
Enriched GO Terms of Interacting Partners?
Tagcloud ?
17q  17q12  amplicon  amplification  amplifications  amplified  anthracycline  besides  ccr7  concerning  gast  grb7  heterogeneity  heterogeneous  igfpb4  iia  implications  krt19  locus  med1  pitfalls  presents  rara  stard3  subgroup  thra  top2a  topoisomerase  variations 
17p13  adipocytes  array  cgh  disability  duplication  dysmorphic  encodes  encompassing  facial  fingers  fissures  glut4  hyperpigmentation  intellectual  mandible  nlgn2  nostrils  obesity  p13  palpebral  proposita  recognizable  referred  seizures  slc2a4  slender  tp53  upturned 
Tagcloud (Difference) ?
17q  17q12  amplicon  amplification  amplifications  amplified  anthracycline  besides  ccr7  concerning  gast  grb7  heterogeneity  heterogeneous  igfpb4  iia  implications  krt19  locus  med1  pitfalls  presents  rara  stard3  subgroup  thra  top2a  topoisomerase  variations 
17p13  adipocytes  array  cgh  disability  duplication  dysmorphic  encodes  encompassing  facial  fingers  fissures  glut4  hyperpigmentation  intellectual  mandible  nlgn2  nostrils  obesity  p13  palpebral  proposita  recognizable  referred  seizures  slc2a4  slender  tp53  upturned 
Tagcloud (Intersection) ?