solute carrier family 5 member 7
| UniProt | Protein Name |
|---|---|
| B2RCU2 |
|
| B4DUU7 |
|
| Q2T9H3 |
|
| Q9GZV3 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| in utero embryonic development |
|
|
| sodium ion transport |
|
|
| neurotransmitter transport |
|
|
| synaptic transmission, cholinergic |
|
|
| neuromuscular synaptic transmission |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| choline:sodium symporter activity |
|
|
| choline:sodium symporter activity |
|
|
| choline:sodium symporter activity |
|
|
| choline:sodium symporter activity |
|
|
| choline transmembrane transporter activity |
|
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:1596 | depressive disorder | |
| DOID:0111199 | autosomal dominant distal hereditary motor neuronopathy 7 | |
| DOID:0110661 | congenital myasthenic syndrome 20 |
| Species | Gene ID | Alliance of Genome Resources |
|---|---|---|
| 63993 | MGI:1927126 | |
| 85426 | RGD:69270 | |
| 178274 | WB:WBGene00000501 | |
| 42245 | FB:FBgn0038641 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: April 6, 2026