| Name | fragile site, folic acid type, rare, fra(16)(p13.11) |
| Description | There are several phenotypes associated with variation in pericentric region of chromosome 16: see the 16p12.2-p11.2 deletion syndrome (MIM 613604); see MIM 611913 for a deletion or duplication at 16p11.2 associated with autism (AUTS14); and see MIM 613444 for a 220-kb deletion at 16p11.2 associated with isolated severe early-onset obesity and obesity with developmental delay.[supplied by OMIM, Nov 2010] |
| NCBI Gene ID | 2460 |
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| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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FRA16A has 2 functional associations with biological entities spanning 1 categories (functional term, phrase or reference) extracted from 1 datasets.
Click the + buttons to view associations for FRA16A from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| Biocarta Pathways | pathways involving FRA16A protein from the Biocarta Pathways dataset. | |
