|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|
|Expression in Tissues and Cell Lines||
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
|Biocarta Pathways||pathways involving FRA16A protein from the Biocarta Pathways dataset.|