FRA12A Gene

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
API
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Predicted Functions View FRA12A's ARCHS4 Predicted Functions.
Co-expressed Genes View FRA12A's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View FRA12A's ARCHS4 Predicted Functions.

Functional Associations

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

Dataset Summary
CTD Gene-Disease Associations diseases associated with FRA12A gene/protein from the curated CTD Gene-Disease Associations dataset.