solute carrier family 6 member 8
| GO Term | Evidence Code | PMID |
|---|---|---|
| creatine metabolic process |
|
|
| neurotransmitter transport |
|
|
| amino acid transport |
|
|
| muscle contraction |
|
|
| gamma-aminobutyric acid transport |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| plasma membrane |
|
|
| plasma membrane |
|
|
| plasma membrane |
|
|
| plasma membrane |
|
|
| membrane |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| creatine transmembrane transporter activity |
|
|
| creatine:sodium symporter activity |
|
|
| creatine:sodium symporter activity |
|
|
| creatine:sodium symporter activity |
|
|
| creatine:sodium symporter activity |
|
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050800 | cerebral creatine deficiency syndrome 1 | |
| DOID:1059 | intellectual disability |
| Species | Gene ID | Alliance of Genome Resources |
|---|---|---|
| 102857 | MGI:2147834 | |
| 50690 | RGD:619711 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
GlyCosmos Portal v4.5.0
Last updated: April 6, 2026