|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]|
|NCBI Gene ID||1637|
|Expression in Tissues and Cell Lines||
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
|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.|