GO Term |
---|
extracellular region |
basement membrane |
extracellular space |
plasma membrane |
axon |
collagen-containing extracellular matrix |
plasma membrane protein complex |
neuronal cell body |
extracellular exosome |
Golgi lumen |
Position | Description | PubMed ID | GlyTouCan ID | Source |
---|---|---|---|---|
1920 |
|
|||
1926 |
|
|||
2121 | N-linked (GlcNAc...) asparagine | |||
2127 |
|
|||
2136 |
|
|||
2138 |
|
|||
2140 |
|
|||
2143 |
|
|||
2145 |
|
|||
2150 |
|
Pathway Name | Organism |
---|---|
A tetrasaccharide linker sequence is required for GAG synthesis | Homo sapiens |
Amyloid fiber formation | Homo sapiens |
Attachment and Entry | Homo sapiens |
Defective B3GALT6 causes EDSP2 and SEMDJL1 | Homo sapiens |
Defective B3GAT3 causes JDSSDHD | Homo sapiens |
Defective B4GALT7 causes EDS, progeroid type | Homo sapiens |
Defective EXT1 causes exostoses 1, TRPS2 and CHDS | Homo sapiens |
Defective EXT2 causes exostoses 2 | Homo sapiens |
Degradation of the extracellular matrix | Homo sapiens |
ECM proteoglycans | Homo sapiens |
DO ID | Disease Name | Source |
---|---|---|
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 | |
DOID:0110304 | autosomal dominant limb-girdle muscular dystrophy type 2 |
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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