Gene Name | dyskeratosis congenita 1, dyskerin | |
Image | No pdb structure | |
Gene Ontology Annotations | Cellular Component | |
Molecular Function | ||
Biological Process | ||
Pathways | ||
Drugs | ||
Diseases | ||
GWAS | ||
Protein-protein Interactions | 10 interactors: CSNK2A1 EEF1G EIF3F ERG LYPLA2 MAPK6 RUVBL1 SHQ1 SSR1 TERC | |
Entrez ID | 1736 | |
HPRD ID | 02129 | |
Ensembl ID | ENSG00000130826 | |
Uniprot IDs | O60832 | |
PDB IDs | ||
Enriched GO Terms of Interacting Partners? |
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Tagcloud ? | aneuploidy
aplastic
attrition
circumstances
complexly
congenita
constitutional
cryptic
delineated
destabilize
dyskeratosis
enforcing
etiologic
helpful
mucocutaneous
multiorgan
oncogenesis
prominent
recessive
regenerative
revision
shelterin
shorten
stereotypical
subtle
telomere
telomeropathy
terc
tert
|