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Literature summary for 3.5.1.26 extracted from

  • Jackson, M.; Clayton, P.; Grunewald, S.; Keir, G.; Mills, K.; Mills, P.; Winchester, B.; Worthington, V.; Young, E.
    Elevation of plasma aspartylglucosaminidase is a useful marker for the congenital disorders of glycosylation type I (CDG I) (2005), J. Inherit. Metab. Dis., 28, 1197-1198.
    View publication on PubMed
Search for more literature for 3.5.1.26

Application

Application Comment Organism
diagnostics elevation of plasma aspartylglucosaminidase is a useful marker for the congenital disorders of glycosylation type I, CDG I Homo sapiens

Localization

Localization Comment Organism GeneOntology No. Textmining
extracellular plasma Homo sapiens
-
-

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
additional information Homo sapiens enzyme level in plasma is elevated in congenital disorders of glycosylation type I, CDG I, a defect in biosynthesis or processing of O-linked glycans, overview ?
-
 ?

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
blood plasma
-
 Homo sapiens
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information enzyme level in plasma is elevated in congenital disorders of glycosylation type I, CDG I, a defect in biosynthesis or processing of O-linked glycans, overview Homo sapiens ?
-
 ?

Synonyms

Synonyms Comment Organism
AGA
-
 Homo sapiens
aspartylglucosaminidase
-
 Homo sapiens