| HGNC Family | X-linked mental retardation |
| Name | mental retardation, X-linked 52 |
| NCBI Gene ID | 4415 |
| 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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MRX52 has 2 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 2 datasets.
Click the + buttons to view associations for MRX52 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| CTD Gene-Disease Associations | diseases associated with MRX52 gene/protein from the curated CTD Gene-Disease Associations dataset. | |
| OMIM Gene-Disease Associations | phenotypes associated with MRX52 gene from the curated OMIM Gene-Disease Associations dataset. | |