GO Term | Evidence Code | PMID |
---|---|---|
axon | ||
postsynapse | ||
neuronal cell body | ||
synapse | ||
cell surface |
GO Term | Evidence Code | PMID |
---|---|---|
P-type sodium:potassium-exchanging transporter activity | ||
transporter activity | ||
amyloid-beta binding | ||
P-type sodium:potassium-exchanging transporter activity involved in regulation of cardiac muscle cell membrane potential | ||
protein-folding chaperone binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050635 | alternating hemiplegia of childhood | |
DOID:0060178 | familial hemiplegic migraine | |
DOID:0070385 | developmental and epileptic encephalopathy 99 | |
DOID:0090056 | dystonia 12 | |
DOID:1574 | alcohol use disorder | |
DOID:1826 | epilepsy | |
DOID:3312 | bipolar disorder | |
DOID:863 | nervous system disease |
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115173532 | SALTR105671 | ||
115175937 | SALTR03487 | ||
115177268 | SALTR85616 | ||
115553528 | GADMO05341 | ||
101159291 | ORYLA05898 | ||
101168472 | ORYLA01925 | ||
100712391 | ORENI05715 | ||
115566854 | SPAAU60551 | ||
115578835 | SPAAU21813 | ||
100145440 | Xenbase:XB-GENE-996131 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024