This gene encodes a member of the ALG3 family. The encoded protein catalyses the addition of the first dol-P-Man derived mannose in an alpha 1,3 linkage to Man5GlcNAc2-PP-Dol. Defects in this gene have been associated with congenital disorder of glycosylation type Id (CDG-Id) characterized by abnormal N-glycosylation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ALG3-20-RE | 20 (40 μL) | 200 μL |  |
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| ALG3-20-OR | 20 (40 μL) | 200 μL |  |
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| ALG3-20-GO | 20 (40 μL) | 200 μL |  |
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| ALG3-20-GR | 20 (40 μL) | 200 μL |  |
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| ALG3-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the ALG3 family. The encoded protein catalyses the addition of the first dol-P-Man derived mannose in an alpha 1,3 linkage to Man5GlcNAc2-PP-Dol. Defects in this gene have been associated with congenital disorder of glycosylation type Id (CDG-Id) characterized by abnormal N-glycosylation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]
Gene Symbol : ALG3
Gene Name : ALG3, alpha-1,3- mannosyltransferase
Chromosome : CHR 3: 184,249,524-184,242,328
Locus : 3q27.1
Alt. Genes : HIPK3
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