UniProt | Protein Name |
---|---|
Q9NQ66 |
|
GO Term | Evidence Code | PMID |
---|---|---|
protein binding | ||
phosphatidylinositol phospholipase C activity | ||
GTPase activator activity | ||
calmodulin binding | ||
identical protein binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:12849 | autistic disorder | |
DOID:1287 | cardiovascular system disease | |
DOID:13378 | Kawasaki disease | |
DOID:14221 | abdominal obesity-metabolic syndrome 1 | |
DOID:1443 | cerebral degeneration | |
DOID:14525 | Reye syndrome | |
DOID:1470 | major depressive disorder | |
DOID:1595 | melancholic depression | |
DOID:1596 | depressive disorder | |
DOID:1612 | breast cancer |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000252 | Microcephaly |
HP:0000505 | Visual impairment |
HP:0000707 | Abnormality of the nervous system |
HP:0000826 | Precocious puberty |
HP:0001252 | Hypotonia |
HP:0001257 | Spasticity |
HP:0001273 | Abnormal corpus callosum morphology |
HP:0001276 | Hypertonia |
HP:0001336 | Myoclonus |
Disease ID | Disease Name |
---|---|
ORPHA:293181 |
|
OMIM:613722 |
|
ORPHA:3451 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115574335 | SPAAU60687 | ||
733258 | Xenbase:XB-GENE-6253450 | ||
108716400 | Xenbase:XB-GENE-17334890 | ||
780394 | Xenbase:XB-GENE-6045753 | ||
101932753 | CHRPI33817 | ||
109319490 | CROPO06907 | ||
113442728 | PSETE15005 | ||
100078508 | ORNAN26848 | ||
100409716 | CALJA32726 | ||
105582092 | CERAT03121 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024