NAGPA Chromosome 16

N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase
1 variant 1 Health Risk

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What This Gene Does
Hydrolases are transported to lysosomes after binding to mannose 6-phosphate receptors in the trans-Golgi network. This gene encodes the enzyme that catalyzes the second step in the formation of the mannose 6-phosphate recognition marker on lysosomal hydrolases. Commonly known as 'uncovering enzyme' or UCE, this enzyme removes N-acetyl-D-glucosamine (GlcNAc) residues from GlcNAc-alpha-P-mannose moieties and thereby produces the recognition marker. The encoded preproprotein is proteolytically processed by furin to generate the mature enzyme, a homotetramer of two disulfide-linked homodimers. Mutations in this gene are associated with developmental stuttering in human patients. [provided by RefSeq, Oct 2015]
Associated Conditions (3)
Stuttering
familial persistent
2
Key Variants
All Variants (1)
RSID Category Clinical Significance Conditions
RS139526942 Health Risk Conflicting classifications of pathogenicity Stuttering, familial persistent, 2
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