MCRS1 and FXR2

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

MCRS1

FXR2

Gene Name microspherule protein 1 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 30 interactors: BLM CCDC53 CCDC85B CEP44 DAXX DVL2 FXR2 GCC1 GPBP1 IKZF1 KDM1A KIAA1958 KXD1 LIG4 LSM6 MAGEA11 MED4 NOP2 PBX2 PHC2 PINX1 PRMT5 RALYL SUV39H1 TERT TRIM37 UPF3B USHBP1 WBP11 ZBTB22 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 10445 9513
HPRD ID 11298 05629
Ensembl ID ENSG00000187778 ENSG00000129245
Uniprot IDs Q7Z372 Q96EZ8 P51116
PDB IDs 3H8Z
Enriched GO Terms of Interacting Partners?
Tagcloud ?
acetylates  akhtar  buscaino  duncan  gebhardt  h4k16  hcf1  holz  ino80  mendjan  mof  moz  msl  mueller  myst  myst1  nsl  nucleosomal  relaxed  sas2  sas3  saumweber  schelder  stunnenberg  taipale  vermeulen  wdr5  wilm  ybf2 
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) ?
acetylates  akhtar  buscaino  duncan  gebhardt  h4k16  hcf1  holz  ino80  mendjan  mof  moz  msl  mueller  myst  myst1  nsl  nucleosomal  relaxed  sas2  sas3  saumweber  schelder  stunnenberg  taipale  vermeulen  wdr5  wilm  ybf2 
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) ?