GO Term |
---|
osteoblast development |
acetylcholine catabolic process |
cell adhesion |
nervous system development |
synapse assembly |
GO Term |
---|
membrane |
neuromuscular junction |
synapse |
Position | Description | PubMed ID | GlyTouCan ID | Source |
---|---|---|---|---|
296 | N-linked (GlcNAc...) asparagine | |||
381 | N-linked (GlcNAc...) asparagine | |||
495 | N-linked (GlcNAc...) asparagine |
|
Pathway Name | Organism |
---|---|
Neurotransmitter clearance | Homo sapiens |
Synthesis of PC | Homo sapiens |
Synthesis, secretion, and deacylation of Ghrelin | Homo sapiens |
DO ID | Disease Name | Source |
---|---|---|
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 | |
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 |
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Last updated: August 19, 2024