RBFOX3 Chromosome 17

RNA binding fox-1 homolog 3
5 variants 5 Health Risk

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What This Gene Does
This gene encodes a member of the RNA-binding FOX protein family which is involved in the regulation of alternative splicing of pre-mRNA. The protein has an N-terminal proline-rich region, an RNA recognition motif (RRM) domain, and a C-terminal alanine-rich region. This gene produces the neuronal nuclei (NeuN) antigen that has been widely used as a marker for post-mitotic neurons. This gene has its highest expression in the central nervous system and plays a prominent role in neural tissue development and regulation of adult brain function. Mutations in this gene have been associated with numerous neurological disorders. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, May 2017]
Gene Info
Gene Group
"RNA binding motif containing|RNA binding fox-1 homologs"
Locus Type
gene with protein product
Location
17q25.3
Ensembl
ENSG00000167281
Associated Conditions (3)
Idiopathic generalized epilepsy
RBFOX3-related disorder
Self-limited epilepsy with centrotemporal spikes
Key Variants
All Variants (5)
RSID Category Clinical Significance Conditions
RS112978510 Health Risk Conflicting classifications of pathogenicity Idiopathic generalized epilepsy, RBFOX3-related disorder, Idiopathic generalized epilepsy
RS199891032 Health Risk Conflicting classifications of pathogenicity Idiopathic generalized epilepsy, Idiopathic generalized epilepsy
RS375309858 Health Risk Conflicting classifications of pathogenicity Idiopathic generalized epilepsy, Idiopathic generalized epilepsy
RS376060745 Health Risk Conflicting classifications of pathogenicity Idiopathic generalized epilepsy, Idiopathic generalized epilepsy
RS972548690 Health Risk Pathogenic Self-limited epilepsy with centrotemporal spikes, Self-limited epilepsy with centrotemporal spikes
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