rs764871960

This variant is located in the MSTO1 gene.

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ClinVar annotation

Conflicting Classifications
4 submitters1 publication

Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome; Inborn genetic diseases; Congenital cerebellar hypoplasia

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About MSTO1

Involved in mitochondrion distribution; mitochondrion organization; and positive regulation of mitochondrial fusion. Located in mitochondrial outer membrane. Is active in cytosol. [provided by Alliance of Genome Resources, Jul 2025]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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