rs929689129
This variant is located in the DOK7 gene.
▶ClinVar annotation
Fetal akinesia deformation sequence 1;Congenital myasthenic syndrome 10
View on ClinVar →About DOK7
The protein encoded by this gene is essential for neuromuscular synaptogenesis. The protein functions in aneural activation of muscle-specific receptor kinase, which is required for postsynaptic differentiation, and in the subsequent clustering of the acetylcholine receptor in myotubes. This protein can also induce autophosphorylation of muscle-specific receptor kinase. Mutations in this gene are a cause of familial limb-girdle myasthenia autosomal recessive, which is also known as congenital myasthenic syndrome type 1B. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
View all DOK7 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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