DCX

Gene Name doublecortin
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Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-protein Interactions 29 interactors: ACD AP1M1 AP2M1 APP CALCOCO2 CDK5 FBXO25 GOLGA2 IKZF1 KIFC3 KRT40 KRTAP10-8 MEOX1 MID2 NFASC PAFAH1B1 POT1 PPP1CA PPP1R9B RINT1 SPAG5 SPP1 TERF1 TINF2 TRIM23 TRIM27 TRIM39 USP9X ZBTB5
Entrez ID 1641
HPRD ID 02127
Ensembl ID ENSG00000077279
Uniprot IDs A8K340 B4DM53 O43602
PDB IDs 1MJD 2BQQ 2XRP 4ATU
Enriched GO Terms of Interacting Partners?
Tagcloud ?
17p13  classical  deletions  disrupt  epilepsy  frontal  gradient  lis  lis1  lissencephaly  malformation  mutations  occipital  overlapping  parietal  proline  q23  repeats  retardation  sequencing  sexes  southern  splice  sporadic  though  truncation  wd40  xlis  xq22