dolichyl-phosphate mannosyltransferase subunit 3, regulatory
| UniProt | Protein Name |
|---|---|
| Q9P2X0 |
|
| A0A140VJI4 |
|
| Q86TM7 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| glycoprotein biosynthetic process |
|
|
| protein O-linked glycosylation via mannose |
|
|
| dolichyl monophosphate biosynthetic process |
|
|
| dolichol phosphate mannose biosynthetic process |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum |
|
|
| endoplasmic reticulum membrane |
|
|
| endoplasmic reticulum membrane |
|
|
| endoplasmic reticulum membrane |
|
|
| endoplasmic reticulum membrane |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding |
|
|
| enzyme activator activity |
|
|
| protein-membrane adaptor activity |
|
| InterPro |
|---|
| Dolichol-phosphate mannosyltransferase subunit 3 |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
| Species | Protein | mRNA |
|---|---|---|
| Mus musculus | NP_081043 | NM_026767 |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050570 | congenital disorder of glycosylation type I | |
| DOID:0112376 | muscular dystrophy-dystroglycanopathy type B15 |
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0001270 | Motor delay |
| HP:0001315 | Reduced tendon reflexes |
| HP:0001324 | Muscle weakness |
| HP:0001644 | Dilated cardiomyopathy |
| HP:0001763 | Pes planus |
| HP:0002121 | Generalized non-motor (absence) seizure |
| HP:0002187 | Intellectual disability, profound |
| HP:0002317 | Unsteady gait |
| HP:0002401 | Stroke-like episode |
| Disease ID | Disease Name |
|---|---|
| OMIM:612937 |
|
| ORPHA:263494 |
|
| OMIM:618992 |
|
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: April 6, 2026