DCR Gene

Name Down syndrome chromosome region
Description Down syndrome, the most frequent form of mental retardation caused by a microscopically demonstrable chromosomal aberration, is characterized by well-defined and distinctive phenotypic features and natural history. It is caused by triplicate state (trisomy) of all or a critical portion of chromosome 21.[supplied by OMIM, Apr 2005]
Synonyms DSCR
NCBI Gene ID 1637
API
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Predicted Functions View DCR's ARCHS4 Predicted Functions.
Co-expressed Genes View DCR's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View DCR's ARCHS4 Predicted Functions.

Functional Associations

DCR has 52 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 3 datasets.

Click the + buttons to view associations for DCR from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
CTD Gene-Disease Associations diseases associated with DCR gene/protein from the curated CTD Gene-Disease Associations dataset.
MPO Gene-Phenotype Associations phenotypes of transgenic mice caused by DCR gene mutations from the MPO Gene-Phenotype Associations dataset.
OMIM Gene-Disease Associations phenotypes associated with DCR gene from the curated OMIM Gene-Disease Associations dataset.