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ALG6

ALG6

Protein-coding gene in the species Homo sapiens

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

ALG6

ALG6 (enzyme class)

Class of enzymes

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

ALG6 (enzyme class)

ALG6_(enzyme_class)

Congenital disorder of glycosylation

Medical condition

rod function on electroretinography. Three CDG subtypes PMM2-CDG, PMI-CDG, ALG6-CDG can cause congenital hyperinsulinism with hyperinsulinemic hypoglycemia

Congenital disorder of glycosylation

Congenital_disorder_of_glycosylation

List of human protein-coding genes 1

HGNC:23159; Q9H553 567 ALG3 HGNC:23056; Q92685 568 ALG5 HGNC:20266; Q9Y673 569 ALG6 HGNC:23157; Q9Y672 570 ALG8 HGNC:23161; Q9BVK2 571 ALG9 HGNC:15672; Q9H6U8

List of human protein-coding genes 1

List_of_human_protein-coding_genes_1

ALG8

Protein-coding gene in the species Homo sapiens

enzyme encoded in humans by the ALG8 gene. This gene encodes a member of the ALG6/ALG8 glucosyltransferase family. The encoded protein catalyzes the addition

ALG8

List of OMIM disorder codes

Ia; 212065; PMM2 Congenital disorder of glycosylation, type Ic; 603147; ALG6 Congenital disorder of glycosylation, type Id; 601110; ALG3 Congenital disorder

List of OMIM disorder codes

List_of_OMIM_disorder_codes

Online names & meanings

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Girl/Female

Tamil

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Wignall

Surname or Lastname

English (Lancashire)

Wignall

English (Lancashire) : habitational name from Wignal, a minor place near Holmes in the parish of Croston, so named from the genitive case of the Old English byname Wicga (see Wigley) + Old English h(e)alh â€˜nookâ€™, â€˜cornerâ€™, â€˜recessâ€™.