| Name | Down syndrome chromosome region |
| Description | Down syndrome, also known as trisomy 21, is the most frequent form of cognitive disability caused by a microscopically demonstrable chromosomal aberration. It is caused by a third copy (trisomy) of all or a critical portion of chromosome 21. Down syndrome is characterized by physical growth delays, dysmorphic facial features, heart and gastrointestinal disorders, and mild to moderate cognitive disability. [provided by RefSeq, Jul 2017] |
| Synonyms | DSCR |
| NCBI Gene ID | 1637 |
| API | |
| Download Associations | |
| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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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. | |
