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Protein-coding gene in the species Homo sapiens
mannosyltransferase is an enzyme that, in humans, is encoded by the ALG3 gene. This gene encodes a member of the ALG3 family. The encoded protein catalyses the addition
ALG3
Class of enzymes
Man5GlcNAc2-PP-Dol mannosyltransferase, ALG3, dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase, Not56-like protein, Alg3 alpha-1,3-mannosyl transferase
Dolichyl-P-Man:Man5GlcNAc2-PP-dolichol alpha-1,3-mannosyltransferase
Dolichyl-P-Man:Man5GlcNAc2-PP-dolichol_alpha-1,3-mannosyltransferase
Class of enzymes
of alpha-1,6-polymannose outer chain from och1, och1 mnn1, and och1 mnn1 alg3 mutants of Saccharomyces cerevisiae". J. Biol. Chem. 268 (35): 26338–45.
Initiation-specific alpha-1,6-mannosyltransferase
Initiation-specific_alpha-1,6-mannosyltransferase
Medical condition
(MPI-CDG) 602579 MPI 15q22-qter Ic (ALG6-CDG) 603147 ALG6 1p22.3 Id (ALG3-CDG) 601110 ALG3 3q27 Ie (DPM1-CDG) 608799 DPM1 20q13.13 If (MPDU1-CDG) 609180 MPDU1
Congenital disorder of glycosylation
Congenital_disorder_of_glycosylation
HGNC:18294; Q9BT22 565 ALG1L2 HGNC:37258; C9J202 566 ALG2 HGNC:23159; Q9H553 567 ALG3 HGNC:23056; Q92685 568 ALG5 HGNC:20266; Q9Y673 569 ALG6 HGNC:23157; Q9Y672
List of human protein-coding genes 1
List_of_human_protein-coding_genes_1
Ic; 603147; ALG6 Congenital disorder of glycosylation, type Id; 601110; ALG3 Congenital disorder of glycosylation, type Ie; 608799; DPM1 Congenital disorder
List_of_OMIM_disorder_codes
ALG3
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Boy/Male
Tamil
Boy/Male
Muslim/Islamic
Sura in Quran
Girl/Female
Arabic Muslim African
Beautiful.
Boy/Male
Arabic
Most Honourable; Most Precious
Surname or Lastname
English
English : variant of Shapley.Thomas Shapleigh (1765–1800), born in Kittery MA, was librarian of Harvard College in the 1790s.
Boy/Male
Australian, French, German, Greek, Italian
People's Ruler
Girl/Female
Latin
Without conceit; modest.
Boy/Male
Hindu
Sun or brilliant boy
Boy/Male
Hindu
One who accepts all penances
Surname or Lastname
English
English : variant of Harwood.
ALG3
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