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- Table of Contents
Facts about Dol-P-Man:Man(7)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferase.
Human | |
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Gene Name: | ALG12 |
Uniprot: | Q9BV10 |
Entrez: | 79087 |
Belongs to: |
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glycosyltransferase 22 family |
alpha-1,6-mannosyltransferase); asparagine-linked glycosylation 12 homolog (S. cerevisiae; asparagine-linked glycosylation 12 homolog (yeast; asparagine-linked glycosylation 12, alpha-1,6-mannosyltransferase homolog (S.cerevisiae); Asparagine-linked glycosylation protein 12 homolog; CDG1G; dolichyl-P-Man:Man(7)GlcNAc(2)-PP-dolichyl-alpha-1,6-mannosyltransferase; dolichyl-P-mannose:Man-7-GlcNAc-2-PP-dolichyl-alpha-6-mannosyltransferase; EC 2.4.1.-; ECM39; hALG12; Mannosyltransferase ALG12 homolog; Membrane protein SB87; MGC111358; MGC3136; PP14673
Mass (kDA):
54.655 kDA
Human | |
---|---|
Location: | 22q13.33 |
Sequence: | 22; NC_000022.11 (49860163..49918469, complement) |
Expressed in fibroblasts.
Endoplasmic reticulum membrane; Multi-pass membrane protein.
PMID: 11983712 by Chantret I., et al. Congenital disorders of glycosylation type Ig is defined by a deficiency in dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl mannosyltransferase.
PMID: 12217961 by Grubenmann C.E., et al. ALG12 mannosyltransferase defect in congenital disorder of glycosylation type Ig.