GO Term |
---|
lysosome |
lysosomal membrane |
plasma membrane |
membrane |
intracellular membrane-bounded organelle |
azurophil granule membrane |
extracellular exosome |
tertiary granule membrane |
lysosomal lumen |
ficolin-1-rich granule membrane |
GO Term |
---|
carbohydrate binding |
alpha-1,4-glucosidase activity |
alpha-glucosidase activity |
maltose alpha-glucosidase activity |
Position | Description | PubMed ID | GlyTouCan ID | Source |
---|---|---|---|---|
41 |
|
|||
46 |
|
|||
52 |
|
|||
61 |
|
|||
140 | N-linked (GlcNAc...) asparagine | |||
142 |
|
|||
144 |
|
|||
149 |
|
|||
151 |
|
|||
153 |
|
Pathway Name | Organism |
---|---|
GSD II | Homo sapiens |
Glycogen breakdown (glycogenolysis) | Homo sapiens |
Neutrophil degranulation | Homo sapiens |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
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 | |
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 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024