|Name||fragile site, folic acid type, rare, fra(12)(q13.1)|
|Description||FRA12A is a folate-sensitive chromosomal fragile site prone to breakage. No consistent phenotype has been observed with FRA12A, and it can be inherited without phenotypic effect (Berg et al., 2000 [PubMed 10955484]). However, mental retardation with or without other anomalies has been described in patients with over 40% of cells expressing FRA12A (Winnepenninckx et al., 2007).[supplied by OMIM, Mar 2008]|
|NCBI Gene ID||2448|
|Expression in Tissues and Cell Lines||
FRA12A has 1 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 1 datasets.
Click the + buttons to view associations for FRA12A from the datasets below.
If available, associations are ranked by standardized value
|CTD Gene-Disease Associations||diseases associated with FRA12A gene/protein from the curated CTD Gene-Disease Associations dataset.|