CAMK2D and FXR2

  • Number of citations of the paper that reports this interaction (PMID 25416956)
  • 0
  • Data Source:
  • BioGRID (two hybrid)

CAMK2D

FXR2

Gene Name calcium/calmodulin-dependent protein kinase II delta fragile X mental retardation, autosomal homolog 2
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • White matter integrity (interaction) ( 23218918)
Protein-Protein Interactions 27 interactors: ACTN2 ARL2BP BANP CAMK2B CD5 CREM DNAL4 EPHA10 FAM171B FKBP1B FNDC3B FXR2 GRIN2B HDAC4 HNMT IFNGR2 MOAP1 MRPL11 RPS18 RPS4X SPATA24 SRPK1 STAT1 TNPO2 TTC5 VIM WASF3 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 817 9513
HPRD ID 09653 05629
Ensembl ID ENSG00000145349 ENSG00000129245
Uniprot IDs D6R938 E9PF82 Q13557 P51116
PDB IDs 2VN9 2W2C 2WEL 3GP2 3H8Z
Enriched GO Terms of Interacting Partners?
Tagcloud ?
abcc8  acacb  cacna1a  cdkal1  chi  csmd1  disequilibrium  exome  glud1  gnas  hnf1a  hyperinsulinism  kcnh6  kcnj10  kcnj11  nos2  notch2  pde4c  pik3r3  probands  ryr3  scn8a  slc24a6  slc37a3  sulf1  tdt  tll1  trpc5  trpv3 
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) ?
abcc8  acacb  cacna1a  cdkal1  chi  csmd1  disequilibrium  exome  glud1  gnas  hnf1a  hyperinsulinism  kcnh6  kcnj10  kcnj11  nos2  notch2  pde4c  pik3r3  probands  ryr3  scn8a  slc24a6  slc37a3  sulf1  tdt  tll1  trpc5  trpv3 
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) ?