rs750748055

This variant is located in the AGRN gene.

ClinVar annotation

Likely Benign★★★
2 submitters2 publications

Congenital myasthenic syndrome 8; not provided

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About AGRN

This gene encodes one of several proteins that are critical in the development of the neuromuscular junction (NMJ), as identified in mouse knock-out studies. The encoded protein contains several laminin G, Kazal type serine protease inhibitor, and epidermal growth factor domains. Additional post-translational modifications occur to add glycosaminoglycans and disulfide bonds. In one family with congenital myasthenic syndrome affecting limb-girdle muscles, a mutation in this gene was found. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2015]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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