UniProt | Protein Name |
---|---|
Q2WEA5 |
|
GO Term | Evidence Code | PMID |
---|---|---|
signal transduction | ||
protein localization |
GO Term | Evidence Code | PMID |
---|---|---|
monoatomic cation transmembrane transporter activity | ||
calcium channel activity | ||
ion channel activity | ||
monoatomic ion channel activity | ||
monoatomic cation channel activity |
Gene Ontology |
---|
calcium channel activity |
monoatomic ion channel activity |
monoatomic ion transport |
protein tetramerization |
InterPro |
---|
TRPM, SLOG domain |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050534 | congenital stationary night blindness | |
DOID:0060394 | chromosome 15q13.3 microdeletion syndrome | |
DOID:0110867 | congenital stationary night blindness 1C |
Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|---|
101608012 | 51337_0:0010c7 | |||
101675742 | MUSPF10388 | |||
101720797 | 10181_0:002307 | |||
101844705 | 10036_0:000532 | |||
101868141 | MELUD12060 | |||
101937599 | CHRPI06880 | |||
101975745 | 43179_0:004713 | ICTTR14394 | ||
101994877 | 79684_0:0028bd | |||
102017234 | 34839_0:00105a | |||
102182733 | CAPHI13606 |
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Last updated: December 9, 2024