GO Term | Evidence Code | PMID |
---|---|---|
acetylcholine biosynthetic process | ||
neuromuscular synaptic transmission | ||
phosphatidylcholine biosynthetic process |
|
|
neurotransmitter transport |
|
GO Term | Evidence Code | PMID |
---|---|---|
choline O-acetyltransferase activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0110048 | Alzheimer's disease 15 | |
DOID:0110671 | congenital myasthenic syndrome 6 | |
DOID:0110672 | congenital myasthenic syndrome 21 | |
DOID:0110741 | type 1 diabetes mellitus 2 | |
DOID:0110742 | type 1 diabetes mellitus 3 | |
DOID:0110743 | type 1 diabetes mellitus 4 | |
DOID:0110744 | type 1 diabetes mellitus 5 | |
DOID:0110745 | type 1 diabetes mellitus 6 | |
DOID:0110746 | type 1 diabetes mellitus 7 | |
DOID:0110747 | type 1 diabetes mellitus 8 |
HPO ID | HPO Term |
---|---|
HP:0003388 | Easy fatigability |
HP:0003397 | Generalized hypotonia due to defect at the neuromuscular junction |
HP:0003402 | Decreased miniature endplate potentials |
HP:0003403 | EMG: decremental response of compound muscle action potential to repetitive nerve stimulation |
HP:0003458 | EMG: myopathic abnormalities |
HP:0003473 | Fatigable weakness |
HP:0003554 | Type 2 muscle fiber atrophy |
HP:0003577 | Congenital onset |
HP:0003623 | Neonatal onset |
HP:0003693 | Distal amyotrophy |
Disease ID | Disease Name |
---|---|
OMIM:254210 |
|
ORPHA:98914 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
24105307 | WB:WBGene00000481 | ||
42249 | FB:FBgn0000303 | ||
445622 | CIOIN00638 | ||
103181719 | CALMI02473 | ||
100170938 | ZFIN:ZDB-GENE-080102-2 | DANRE06149 | |
103171573 | ZFIN:ZDB-GENE-140429-2 | ||
103044316 | ASTMX06615 | ||
108262900 | ICTPU26813 | ||
113581952 | ELEEL28676 | ||
115560082 | GADMO16433 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024