FRA16A Gene

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
API
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Predicted Functions View FRA16A's ARCHS4 Predicted Functions.
Co-expressed Genes View FRA16A's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View FRA16A's ARCHS4 Predicted Functions.

Functional Associations

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.