UniProt | Protein Name |
---|---|
Q9NQ66 |
|
GO Term | Evidence Code | PMID |
---|---|---|
ligand-gated ion channel signaling pathway | ||
postsynaptic modulation of chemical synaptic transmission | ||
regulation of G protein-coupled receptor signaling pathway | ||
signal transduction |
|
|
positive regulation of G1/S transition of mitotic cell cycle |
GO Term | Evidence Code | PMID |
---|---|---|
enzyme binding | ||
phospholipase C activity |
|
|
phosphatidylinositol-4,5-bisphosphate binding | ||
calcium ion binding | ||
lamin binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050453 | lissencephaly | |
DOID:0050562 | West syndrome | |
DOID:0050709 | early infantile epileptic encephalopathy | |
DOID:0050742 | nicotine dependence | |
DOID:0050759 | myotonic dystrophy type 2 | |
DOID:0050841 | focal hand dystonia | |
DOID:0050848 | obstructive sleep apnea | |
DOID:0050908 | myelodysplastic syndrome | |
DOID:0060041 | autism spectrum disorder | |
DOID:0060306 | Meier-Gorlin syndrome |
HPO ID | HPO Term |
---|---|
HP:0001347 | Hyperreflexia |
HP:0001508 | Failure to thrive |
HP:0002059 | Cerebral atrophy |
HP:0002069 | Bilateral tonic-clonic seizure |
HP:0002376 | Developmental regression |
HP:0002384 | Focal impaired awareness seizure |
HP:0002521 | Hypsarrhythmia |
HP:0002540 | Inability to walk |
HP:0002650 | Scoliosis |
HP:0003593 | Infantile onset |
Disease ID | Disease Name |
---|---|
ORPHA:293181 |
|
OMIM:613722 |
|
ORPHA:3451 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100481755 | AILME10778 | ||
101678347 | MUSPF13915 | ||
101092262 | FELCA06421 | ||
122215803 | PANLE01136 | ||
118881571 | BALMU20704 | ||
100051558 | HORSE21214 | ||
100152679 | PIGXX11241 | ||
287026 | BOVIN04202 | ||
102188148 | CAPHI03220 | ||
101103585 | SHEEP04084 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024