Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
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:0110294 | autosomal recessive limb-girdle muscular dystrophy type 2T | |
| DOID:0110295 | autosomal recessive limb-girdle muscular dystrophy type 2U | |
| DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | |
| DOID:0110297 | autosomal recessive limb-girdle muscular dystrophy type 2K | |
| DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | |
| DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | |
| DOID:0110300 | obsolete autosomal dominant limb-girdle muscular dystrophy type 1A | |
| DOID:0110301 | obsolete autosomal dominant limb-girdle muscular dystrophy type 1B | |
| DOID:0110302 | obsolete autosomal dominant limb-girdle muscular dystrophy type 1C | |
| DOID:0110303 | autosomal dominant limb-girdle muscular dystrophy type 1H |
- 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 |
|---|---|---|---|
| 105985553 | DIPOR06610 | ||
| 100773620 | CRIGR14710 | ||
| 69983 | MGI:1917233 | MOUSE36529 | |
| 497756 | RGD:3675 | RATNO24201 | |
| 100731286 | CAVPO14432 | ||
| 101565602 | OCTDE24319 | ||
| 100013945 | MONDO32241 | ||
| 103664425 | URSMA27392 | ||
| 114053115 | VOMUR06846 | ||
| 113899066 | BOBOX29152 |
