Gene Name | doublecortin | |
Image | ||
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? |
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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
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