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Protein Page:
GNPTG (human)

GNPTG the gamma subunit of N-acetylglucosamine-1-phosphotransferase. May recognize the substrate of GlcNAc-1-phosphotransferase but also lysosomal proteins with mannose-6-phosphate residues. Defects in GNPTG cause a variant of pseudo-Hurler polydystrophy, an autosomal recessive disease of lysosomal hydrolase trafficking. Note: This description may include information from UniProtKB.
Protein type: Secreted; Secreted, signal peptide
Chromosomal Location of Human Ortholog: 16p13.3
Cellular Component: Golgi apparatus
Molecular Function: protein homodimerization activity
Biological Process: carbohydrate phosphorylation
Disease: Mucolipidosis Iii Gamma
Reference #:  Q9UJJ9 (UniProtKB)
Alt. Names/Synonyms: C16orf27; GlcNAc-1-phosphotransferase subunit gamma; GNPTAG; GNPTG; LP2537; N-acetylglucosamine-1-phosphate transferase, gamma subunit; N-acetylglucosamine-1-phosphotransferase subunit gamma; RJD9; UDP-N-acetylglucosamine-1-phosphotransferase subunit gamma
Gene Symbols: GNPTG
Molecular weight: 33,974 Da
Basal Isoelectric point: 6.47  Predict pI for various phosphorylation states
Select Structure to View Below


Protein Structure Not Found.

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