Gene: FXR1
Alternate names for this Gene: FXR1P|MYOPMIL|MYORIBF
Gene Summary: The protein encoded by this gene is an RNA binding protein that interacts with the functionally-similar proteins FMR1 and FXR2. These proteins shuttle between the nucleus and cytoplasm and associate with polyribosomes, predominantly with the 60S ribosomal subunit. Three transcript variants encoding different isoforms have been found for this gene.
Gene is located in Chromosome: 3
Location in Chromosome : 3q26.33
Description of this Gene: FMR1 autosomal homolog 1
Type of Gene: protein-coding
rs1805576 in
FXR1 gene and
Bipolar Disorder
PMID 26433762 2016 A genome-wide association study of bipolar disorder with comorbid eating disorder replicates the SOX2-OT region.
rs1805576 in
FXR1 gene and
Eating Disorders
PMID 26433762 2016 The most significant genome-wide finding was observed bipolar with comorbid eating disorder vs. controls within SOX2-OT (p=8.9×10(-8) for rs4854912) with a secondary peak in the adjacent FXR1 gene (p=1.2×10(-6) for rs1805576) on chromosome 3q26.33.
rs13076861 in
FXR1 gene and
Intelligence
PMID 31374203 2019 Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways.
PMID 29844566 2018 Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.
rs1805576 in
FXR1 gene and
Other eating disorders
PMID 26433762 2016 A genome-wide association study of bipolar disorder with comorbid eating disorder replicates the SOX2-OT region.
rs13076861 in
FXR1 gene and
Schizophrenia
PMID 31374203 2019 Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways.
PMID 26198764 2015 Genome-wide association study of schizophrenia in Ashkenazi Jews.
PMID 30285260 2019 Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.
PMID 29483656 2018 Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
PMID 31268507 2019 Association of Schizophrenia Risk With Disordered Niacin Metabolism in an Indian Genome-wide Association Study.