rs782746186
This variant is located in the SURF1 gene.
▶ClinVar annotation
Inborn genetic diseases; Leigh syndrome
View on ClinVar →About SURF1
This gene encodes a protein localized to the inner mitochondrial membrane and thought to be involved in the biogenesis of the cytochrome c oxidase complex. The protein is a member of the SURF1 family, which includes the related yeast protein SHY1 and rickettsial protein RP733. The gene is located in the surfeit gene cluster, a group of very tightly linked genes that do not share sequence similarity, where it shares a bidirectional promoter with SURF2 on the opposite strand. Defects in this gene are a cause of Leigh syndrome, a severe neurological disorder that is commonly associated with systemic cytochrome c oxidase deficiency. [provided by RefSeq, Jul 2008]
View all SURF1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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