UniProt | Protein Name |
---|---|
Q2WEA5 |
|
GO Term | Evidence Code | PMID |
---|---|---|
calcium ion import across plasma membrane | ||
retinal rod cell development | ||
monoatomic ion transmembrane transport | ||
visual perception | ||
protein tetramerization |
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 |
---|---|---|---|---|
100059740 | HORSE16450 | |||
100078926 | ORNAN21584 | |||
100216447 | Xenbase:XB-GENE-492528 | |||
100230234 | TAEGU02562 | |||
100343239 | RABIT06592 | |||
100402595 | CALJA37880 | |||
100482862 | AILME07770 | |||
100594435 | NOMLE31646 | |||
100655588 | LOXAF03554 | |||
100719532 | 10141_0:003ade | CAVPO06888 |
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Last updated: December 9, 2024