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]
GeneCards Summary for FRA16A Gene
FRA16A (Fragile Site, Folic Acid Type, Rare, Fra(16)(P13.11)) is a Uncategorized gene. Diseases associated with FRA16A include obesity.