Beta-1,4-galactosyltransferase 7 deficiency (Q103658): Difference between revisions
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Refere-se à deficiência de uma enzima que, em humanos, é codificada pelo gene B4GALT7. A galactosiltransferase I catalisa a síntese da ligação glicosaminoglicano-proteína em proteoglicanos. | |||
| description / en | description / en | ||
This refers to deficiency in an enzyme that in humans is encoded by the B4GALT7 gene. Galactosyltransferase I catalyzes the synthesis of the glycosaminoglycan-protein linkage in proteoglycans. | |||
Revision as of 09:24, 17 August 2026
This refers to deficiency in an enzyme that in humans is encoded by the B4GALT7 gene. Galactosyltransferase I catalyzes the synthesis of the glycosaminoglycan-protein linkage in proteoglycans.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_306751792 |
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| English | Beta-1,4-galactosyltransferase 7 deficiency |
This refers to deficiency in an enzyme that in humans is encoded by the B4GALT7 gene. Galactosyltransferase I catalyzes the synthesis of the glycosaminoglycan-protein linkage in proteoglycans. |
