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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
sucrase-isomaltase
Summary
- Gene Symbol
-
- SI
- Aliases
-
- Alpha-methylglucosidase
- Oligo-1,6-glucosidase
- Oligosaccharide alpha-1,6-glucosidase
- alpha-glucosidase
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Cell membrane
- Direct protein sequencing
- Disease variant
- Disulfide bond
- Glycoprotein
- Glycosidase
- Multifunctional enzyme
- Phosphoprotein
- Reference proteome
- Repeat
- Signal-anchor
- Sulfation
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| P14410 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| polysaccharide digestion | ||
| sucrose catabolic process |
| GO Term | Evidence Code | PMID |
|---|---|---|
| plasma membrane | ||
| apical plasma membrane | ||
| brush border | ||
| Golgi apparatus | ||
| extracellular exosome |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| sucrose alpha-glucosidase activity | ||
| alpha-1,4-glucosidase activity | ||
| carbohydrate binding | ||
| protein binding | ||
| oligo-1,6-glucosidase activity |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
G25153NG
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110304 | autosomal dominant limb-girdle muscular dystrophy type 2 | |
| DOID:0110305 | autosomal dominant limb-girdle muscular dystrophy type 1 | |
| DOID:0110306 | autosomal dominant limb-girdle muscular dystrophy type 3 | |
| DOID:0110970 | brachydactyly type C | |
| DOID:0111040 | glycogen storage disease IXd | |
| DOID:0111041 | glycogen storage disease IXb | |
| DOID:0111042 | glycogen storage disease IXa | |
| DOID:0111043 | glycogen storage disease IXc | |
| DOID:0111633 | congenital sucrase-isomaltase deficiency | |
| DOID:1029 | familial periodic paralysis |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000787 | Nephrolithiasis |
| HP:0001508 | Failure to thrive |
| HP:0002013 | Vomiting |
| HP:0002014 | Diarrhea |
| HP:0002018 | Nausea |
| HP:0002019 | Constipation |
| HP:0002020 | Gastroesophageal reflux |
| HP:0002024 | Malabsorption |
| HP:0002027 | Abdominal pain |
| Disease ID | Disease Name |
|---|---|
| OMIM:222900 |
|
| ORPHA:35122 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 173848 | WB:WBGene00019895 | ||
| 100148922 | ZFIN:ZDB-GENE-030131-4622 | ||
| 100379714 | Xenbase:XB-GENE-964595 | ||
| 100487641 | Xenbase:XB-GENE-996659 | ||
| 100410281 | CALJA15567 | ||
| 105586092 | CERAT22633 | ||
| 102128108 | MACFA26457 | ||
| 700840 | MACMU29561 | ||
| 105466450 | MACNE31674 | ||
| 101010666 | PAPAN26118 |
