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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:0110281 | autosomal recessive limb-girdle muscular dystrophy type 2G | |
| DOID:0110282 | autosomal recessive limb-girdle muscular dystrophy type 2H | |
| DOID:0110283 | autosomal recessive limb-girdle muscular dystrophy type 2J | |
| DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | |
| DOID:0110285 | autosomal recessive limb-girdle muscular dystrophy type 2Q | |
| DOID:0110286 | obsolete autosomal recessive limb-girdle muscular dystrophy type 2R | |
| DOID:0110287 | autosomal recessive limb-girdle muscular dystrophy type 2S | |
| DOID:0110289 | autosomal recessive limb-girdle muscular dystrophy type 2Y | |
| DOID:0110292 | autosomal recessive limb-girdle muscular dystrophy type 2O | |
| DOID:0110293 | autosomal recessive limb-girdle muscular dystrophy type 2P |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002607 | Bowel incontinence |
| HP:0003270 | Abdominal distention |
| HP:0003593 | Infantile onset |
| HP:0004396 | Poor appetite |
| HP:0011848 | Abdominal colic |
| HP:0012378 | Fatigue |
| 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 |
