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 |
---|---|---|---|---|
116894293 | 10117_0:001138 | |||
117018844 | RHIFE27365 | |||
117708375 | 61156_0:0001f7 | |||
118570412 | 38674_0:000527 | |||
118890189 | BALMU29042 | |||
119086620 | 10041_0:000a6a | |||
119802478 | 1047088_0:004370 | |||
121133809 | 10036_0:0001f7 | |||
121134177 | 10036_0:00037f | |||
121456050 | 111838_0:00016f |
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Last updated: December 9, 2024