Mitochondrial glutamate carrier 1 deficiency (Q94615): Difference between revisions
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| description / pt-br | description / pt-br | ||
É uma deficiência expressa predominantemente na membrana plasmática, permitindo a remoção do glutamato do espaço extracelular. Também foi localizado na membrana mitocondrial interna como parte da lançadeira malato-aspartato. | |||
| description / en | description / en | ||
This is a deficiency predominantly expressed in the plasma membrane, allowing it to remove glutamate from the extracellular space. It has also been localised in the inner mitochondrial membrane as part of the malate-aspartate shuttle. | |||
Revision as of 09:55, 16 August 2026
This is a deficiency predominantly expressed in the plasma membrane, allowing it to remove glutamate from the extracellular space. It has also been localised in the inner mitochondrial membrane as part of the malate-aspartate shuttle.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_358582965 |
||
| English | Mitochondrial glutamate carrier 1 deficiency |
This is a deficiency predominantly expressed in the plasma membrane, allowing it to remove glutamate from the extracellular space. It has also been localised in the inner mitochondrial membrane as part of the malate-aspartate shuttle. |
