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Protein-coding gene in humans
transferase subunit ALG13 homolog, also known as asparagine-linked glycosylation 13 homolog, is an enzyme that in humans is encoded by the ALG13 gene. The protein
ALG13
Protein-coding gene in humans
an essential modification that regulates protein folding and stability. ALG13 and ALG14 (this protein) constitute the UDP-GlcNAc transferase, which catalyzes
ALG14
Rare form of childhood-onset epilepsy
syndrome have de novo mutations in a variety of genes, including CHD2, GABRB3, ALG13 and SCN2A. The Epi4K study consortium (2013) observed de novo mutations
Lennox–Gastaut_syndrome
Cytoplasmic biomolecular condensates of proteins and RNA occurring in cells under stress
Protein 13 ALDH18A1 ALDH18A1 Delta-1-pyrroline-5-carboxylate synthase ALG13 ALG13 ALG13, UDP-N-Acetylglucosaminyltransferase Subunit ALPK2 ALPK2/HAK Alpha
Stress_granule
HGNC:31088; Q5I7T1 574 ALG11 HGNC:32456; Q2TAA5 575 ALG12 HGNC:19358; Q9BV10 576 ALG13 HGNC:30881; Q9NP73 577 ALG14 HGNC:28287; Q96F25 578 ALK HGNC:427; Q9UM73
List of human protein-coding genes 1
List_of_human_protein-coding_genes_1
Medical condition
ALG11-CDG (CDG-Ip) Mutations in the other genes involved in these steps (ALG13 and ALG14) are yet to be described. Man5GlcNAc2-PP-Dol The M5GlcNAc2-structure
Congenital disorder of glycosylation
Congenital_disorder_of_glycosylation
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