rs1262402879

This variant is located in the GGPS1 gene.

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ClinVar annotation

Conflicting Classifications
4 submitters2 publications

Myopathy;Sensorineural hearing loss disorder;Premature ovarian insufficiency; Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome; not provided

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About GGPS1

This gene is a member of the prenyltransferase family and encodes a protein with geranylgeranyl diphosphate (GGPP) synthase activity. The enzyme catalyzes the synthesis of GGPP from farnesyl diphosphate and isopentenyl diphosphate. GGPP is an important molecule responsible for the C20-prenylation of proteins and for the regulation of a nuclear hormone receptor. Alternate transcriptional splice variants, both protein-coding and non-protein-coding, have been found for this gene. [provided by RefSeq, Sep 2010]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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