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Fxr1h


Official Full Name
FMR1 autosomal homolog 1
Organism
Mus musculus
Gene ID
14359
Background
Enables mRNA 3'-UTR AU-rich region binding activity; molecular condensate scaffold activity; and ribonucleoprotein complex binding activity. Involved in several processes, including dentate gyrus development; modulation of chemical synaptic transmission; and regulation of gene expression. Located in several cellular components, including costamere; dendritic spine; and ribosome. Is active in several cellular components, including glutamatergic synapse; intracellular membraneless organelle; and postsynapse. Is expressed in several structures, including central nervous system; gut; heart; musculature; and sensory organ. Human ortholog(s) of this gene implicated in congenital myopathy 9A and congenital myopathy 9B. Orthologous to human FXR1 (FMR1 autosomal homolog 1). [provided by Alliance of Genome Resources, Feb 2025]
Synonyms
Fxr1; Fxr1h; Fxr1p; 1110050J02Rik; 9530073J07Rik

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