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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
glucosidase II alpha subunit
Summary
- Gene Symbol
-
- GANAB
- Aliases
-
- G2AN
- GIIA
- GluII
- KIAA0088
- neutral alpha-glucosidase AB
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Direct protein sequencing
- Disease variant
- Disulfide bond
- Endoplasmic reticulum
- Glycoprotein
- Glycosidase
- Golgi apparatus
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Signal
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| carbohydrate metabolic process | ||
| N-glycan processing |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum lumen | ||
| intracellular membrane-bounded organelle | ||
| melanosome | ||
| glucosidase II complex | ||
| membrane |
| GO Term | Evidence Code | PMID |
|---|---|---|
| alpha-glucosidase activity | ||
| glucan 1,3-alpha-glucosidase activity | ||
| carbohydrate binding | ||
| protein binding | ||
| RNA binding |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
G19958IL
G60230HH
G18948TG
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050770 | polycystic liver disease | |
| DOID:0050778 | Meckel syndrome | |
| DOID:0060262 | gallbladder disease | |
| DOID:0080322 | polycystic kidney disease | |
| DOID:0110858 | polycystic kidney disease 1 | |
| DOID:0110859 | polycystic kidney disease 2 | |
| DOID:0110860 | polycystic kidney disease 3 | |
| DOID:2377 | multiple sclerosis | |
| DOID:322 | myelitis | |
| DOID:381 | arthropathy |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000010 | Recurrent urinary tract infections |
| HP:0000083 | Renal insufficiency |
| HP:0000105 | Enlarged kidney |
| HP:0000107 | Renal cyst |
| HP:0000113 | Polycystic kidney dysplasia |
| HP:0000790 | Hematuria |
| HP:0000791 | Uric acid nephrolithiasis |
| HP:0000822 | Hypertension |
| HP:0001407 | Hepatic cysts |
| Disease ID | Disease Name |
|---|---|
| ORPHA:730 |
|
| OMIM:600666 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 179364 | WB:WBGene00009583 | ||
| 180400 | WB:WBGene00018682 | ||
| 49953 | FB:FBgn0027588 | ||
| 100126019 | ZFIN:ZDB-GENE-070928-36 | DANRE36376 | |
| 100334730 | ZFIN:ZDB-GENE-110930-9 | DANRE07276 | |
| 103037165 | ASTMX04691 | ||
| 113585317 | ELEEL35524 | ||
| 113591874 | ELEEL47544 | ||
| 105026714 | ESOLU10830 | ||
| 115168724 | SALTR43273 |
