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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 |
|---|---|---|---|
| 108418252 | PYGNA03852 | ||
| 101966339 | ICTTR05481 | ||
| 103136895 | POEFO05147 | ||
| 101612853 | JACJA07843 | ||
| 118319524 | SCOMX05468 | ||
| 102439836 | MYOLU16626 | ||
| 117030268 | RHIFE29769 | ||
| 103233997 | CHLSB00304 | ||
| 108533581 | RHIBE27136 | ||
| 104679348 | RHIRO09093 |
