UniProt | Protein Name |
---|---|
Q9NQ66 |
|
GO Term | Evidence Code | PMID |
---|---|---|
positive regulation of transcription, DNA-templated | ||
glutamate receptor signaling pathway | ||
negative regulation of transcription, DNA-templated | ||
positive regulation of embryonic development | ||
positive regulation of JNK cascade |
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:0004302 | Functional motor deficit |
HP:0006813 | Focal hemiclonic seizure |
HP:0007334 | Bilateral tonic-clonic seizure with focal onset |
HP:0007359 | Focal-onset seizure |
HP:0008936 | Axial hypotonia |
HP:0010821 | Focal emotional seizure with laughing |
HP:0010841 | Multifocal epileptiform discharges |
HP:0011097 | Epileptic spasm |
HP:0011121 | Abnormal skin morphology |
HP:0012448 | Delayed myelination |
Disease ID | Disease Name |
---|---|
ORPHA:293181 |
|
OMIM:613722 |
|
ORPHA:3451 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
102140615 | MACFA01196 | ||
718387 | MACMU00877 | ||
105481533 | MACNE22582 | ||
100998763 | PAPAN13023 | ||
105552818 | MANLE04157 | ||
101153613 | GORGO22413 | ||
100969660 | PANPA21845 | ||
469875 | PANTR24346 | ||
100434502 | PONAB20766 | ||
485773 | CANLF09304 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024