ALG2 alpha-1,3/1,6-mannosyltransferase
| UniProt | Protein Name |
|---|---|
| A0A0A0MTE0 |
|
| Q9H553 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein glycosylation | ||
| protein N-linked glycosylation | ||
| dolichol-linked oligosaccharide biosynthetic process | ||
| dolichol-linked oligosaccharide biosynthetic process | ||
| dolichol-linked oligosaccharide biosynthetic process |
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum membrane | ||
| endomembrane system | ||
| membrane | ||
| cytoplasmic side of endoplasmic reticulum membrane |
| GO Term | Evidence Code | PMID |
|---|---|---|
| alpha-1,3-mannosyltransferase activity | ||
| alpha-1,3-mannosyltransferase activity | ||
| alpha-1,3-mannosyltransferase activity | ||
| GDP-Man:Man1GlcNAc2-PP-Dol alpha-1,3-mannosyltransferase activity | ||
| protein binding |
| Gene Ontology |
|---|
| GDP-Man |
| GDP-Man |
| alpha-1,3-mannosyltransferase activity |
| oligosaccharide-lipid intermediate biosynthetic process |
| transferase activity |
| InterPro |
|---|
| Glycosyl transferase, family 1 |
| Glycosyltransferase subfamily 4-like, N-terminal domain |
| Mannosyltransferase ALG2 |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
| Species | Protein | mRNA |
|---|---|---|
| Drosophila melanogaster | NP_647772 | NM_139515 |
| Arabidopsis thaliana | NP_178001 | NM_106527 |
| Caenorhabditis elegans | NP_495010 | NM_062609 |
| Mus musculus | NP_064382 | NM_019998 |
| Saccharomyces cerevisiae | CAA96768 | Z72587 |
| Rattus norvegicus | XP_232987 | XM_232987 |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050571 | congenital disorder of glycosylation type II | |
| DOID:0080561 | congenital disorder of glycosylation Ii | |
| DOID:0110669 | congenital myasthenic syndrome 14 |
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000218 | High palate |
| HP:0000252 | Microcephaly |
| HP:0000286 | Epicanthus |
| HP:0000369 | Low-set ears |
| HP:0000407 | Sensorineural hearing impairment |
| HP:0000431 | Wide nasal bridge |
| HP:0000494 | Downslanted palpebral fissures |
| HP:0000505 | Visual impairment |
| HP:0000508 | Ptosis |
| Disease ID | Disease Name |
|---|---|
| ORPHA:353327 |
|
| OMIM:616228 |
|
| OMIM:607906 |
|
| ORPHA:79326 |
|
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
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Last updated: December 8, 2025