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Overview
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Calculated MW: 75 kDa
Observed MW: Refer to figures
Gene Accession: BC001471Please contact us at for specific academic pricing.
Background
This gene encodes a type II transmembrane protein that resides in the Golgi apparatus. It participates in O-mannosyl glycosylation and is specific for alpha linked terminal mannose. Mutations in this gene may be associated with muscle-eye-brain disease and several congenital muscular dystrophies. Alternatively spliced transcript variants that encode different protein isoforms have been described.
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- Properties
- Applications
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Overview