3-glucosyltransferase is an enzyme that in humans is encoded by the ALG6 gene. This gene encodes a member of the ALG6/ALG8 glucosyltransferase family. The encoded protein...
7 KB (904 words) - 13:26, 24 January 2024
Dolichyl-P-Glc:Man9GlcNAc2-PP-dolichol alpha-1,3-glucosyltransferase (EC 2.4.1.267, ALG6, Dol-P-Glc:Man9GlcNAc2-PP-Dol alpha-1,3-glucosyltransferase) is an enzyme...
3 KB (388 words) - 18:39, 23 January 2024
rod function on electroretinography. Three CDG subtypes PMM2-CDG, PMI-CDG, ALG6-CDG can cause congenital hyperinsulinism with hyperinsulinemic hypoglycemia...
41 KB (3,740 words) - 18:14, 25 September 2024
HGNC:23159 Q9H553 565 ALG3 HGNC:23056 Q92685 566 ALG5 HGNC:20266 Q9Y673 567 ALG6 HGNC:23157 Q9Y672 568 ALG8 HGNC:23161 Q9BVK2 569 ALG9 HGNC:15672 Q9H6U8 570...
277 KB (17 words) - 18:34, 6 October 2024
in humans is encoded by the ALG8 gene. This gene encodes a member of the ALG6/ALG8 glucosyltransferase family. The encoded protein catalyzes the addition...
5 KB (640 words) - 17:21, 3 December 2023
Ia; 212065; PMM2 Congenital disorder of glycosylation, type Ic; 603147; ALG6 Congenital disorder of glycosylation, type Id; 601110; ALG3 Congenital disorder...
234 KB (18,877 words) - 15:43, 9 May 2024