| Name | fragile site, folic acid type, rare, fra(X)(q27.3) A (macroorchidism, mental retardation) |
| Synonyms | FMR1 |
| NCBI Gene ID | 2477 |
| 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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FRAXA has 74 functional associations with biological entities spanning 2 categories (disease, phenotype or trait, functional term, phrase or reference) extracted from 4 datasets.
Click the + buttons to view associations for FRAXA from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| GAD Gene-Disease Associations | diseases associated with FRAXA gene in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. | |
| GAD High Level Gene-Disease Associations | diseases associated with FRAXA gene in GWAS and other genetic association datasets from the GAD High Level Gene-Disease Associations dataset. | |
| GeneRIF Biological Term Annotations | biological terms co-occuring with FRAXA gene in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. | |
| HuGE Navigator Gene-Phenotype Associations | phenotypes associated with FRAXA gene by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. | |
