rs146871193
This variant is located in the SLC5A7 gene.
▶ClinVar annotation
Congenital myasthenic syndrome 20;Neuronopathy, distal hereditary motor, type 7A
View on ClinVar →About SLC5A7
This gene encodes a sodium ion- and chloride ion-dependent high-affinity transporter that mediates choline uptake for acetylcholine synthesis in cholinergic neurons. The protein transports choline from the extracellular space into presynaptic terminals for synthesis into acetylcholine. Increased choline uptake results from increased density of this protein in synaptosomal plasma membranes in response to depolarization of cholinergic terminals. Dysfunction of cholinergic signaling has been implicated in various disorders including depression, attention-deficit disorder, and schizophrenia. An allelic variant of this gene is associated with autosomal dominant distal hereditary motor neuronopathy type VIIA. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]
View all SLC5A7 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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