GO Term |
---|
extracellular region |
extracellular space |
synapse |
collagen-containing extracellular matrix |
Golgi lumen |
lysosomal lumen |
perineuronal net |
GO Term |
---|
hyaluronic acid binding |
metal ion binding |
carbohydrate binding |
extracellular matrix structural constituent |
Position | Description | PubMed ID | GlyTouCan ID | Source |
---|---|---|---|---|
22 |
|
|||
23 |
|
|||
30 |
|
|||
61 |
|
|||
65 |
|
|||
105 |
|
|||
126 | N-linked (GlcNAc...) asparagine | |||
239 | N-linked (GlcNAc...) asparagine |
|
||
333 | N-linked (GlcNAc...) asparagine | |||
371 | O-linked (Xyl...) (keratan sulfate) threonine |
Pathway Name | Organism |
---|---|
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) | Homo sapiens |
Defective CHST6 causes MCDC1 | Homo sapiens |
Defective ST3GAL3 causes MCT12 and EIEE15 | Homo sapiens |
Degradation of the extracellular matrix | Homo sapiens |
ECM proteoglycans | Homo sapiens |
Keratan sulfate biosynthesis | Homo sapiens |
Keratan sulfate degradation | Homo sapiens |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0090078 | hypogonadotropic hypogonadism 7 with or without anosmia | |
DOID:0110273 | autosomal dominant limb-girdle muscular dystrophy | |
DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | |
DOID:0110275 | autosomal recessive limb-girdle muscular dystrophy type 2A | |
DOID:0110276 | autosomal recessive limb-girdle muscular dystrophy type 2B | |
DOID:0110277 | autosomal recessive limb-girdle muscular dystrophy type 2C | |
DOID:0110278 | autosomal recessive limb-girdle muscular dystrophy type 2D | |
DOID:0110279 | autosomal recessive limb-girdle muscular dystrophy type 2E | |
DOID:0110280 | autosomal recessive limb-girdle muscular dystrophy type 2F | |
DOID:0110281 | autosomal recessive limb-girdle muscular dystrophy type 2G |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: August 19, 2024