FRAXA (fragile site, folic acid type, rare, fra(X)(q27.3) A)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 108684022 |
| Gene name | Fragile site, folic acid type, rare, fra(X)(q27.3) A |
| Gene symbol | FRAXA |
| Synonyms (NCBI Gene) |
FMR1
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| Chromosome | X |
| Chromosome location | Xq27.3 |
| Summary | This biological region is found near the 5` regulatory region of the fragile X mental retardation 1 (FMR1) gene on the q arm of chromosome 27, and contains a CGG trinucleotide repeat with AGG repeat interruptions. This region is highly polymorphic, and al |
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miRNA
miRNA information provided by mirtarbase database.
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Related Genes
Genes most often co-reported with FRAXA across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to FRAXA (see Related Genes above), that are NOT already directly curated for FRAXA itself -- a lead worth checking, not a confirmed association.
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