Polypeptide N-acetylgalactosaminyl transferase deficiency (Q103638): Difference between revisions
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| description / pt-br | description / pt-br | ||
Refere-se à deficiência da enzima pertencente à família das glicosiltransferases, especificamente as hexosiltransferases. Esta enzima participa da biossíntese de o-glicano e das estruturas de glicano - biossíntese 1. Possui 2 cofatores: manganês e cálcio. | |||
| description / en | description / en | ||
This refers to deficiency in the enzyme belongs to the family of glycosyltransferases, specifically the hexosyltransferases. This enzyme participates in o-glycan biosynthesis and glycan structures - biosynthesis 1. It has 2 cofactors: manganese, and calcium. | |||
Revision as of 09:23, 17 August 2026
This refers to deficiency in the enzyme belongs to the family of glycosyltransferases, specifically the hexosyltransferases. This enzyme participates in o-glycan biosynthesis and glycan structures - biosynthesis 1. It has 2 cofactors: manganese, and calcium.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1991104308 |
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| English | Polypeptide N-acetylgalactosaminyl transferase deficiency |
This refers to deficiency in the enzyme belongs to the family of glycosyltransferases, specifically the hexosyltransferases. This enzyme participates in o-glycan biosynthesis and glycan structures - biosynthesis 1. It has 2 cofactors: manganese, and calcium. |
