Phosphoenolpyruvate carboxykinase 1 deficiency (Q99797): Difference between revisions
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Refere -se a uma deficiência enzimática que em humanos é codificada pelo gene PCK1. Esta é uma enzima da família da liase usada na via metabólica da gliconeogênese. Ela converte oxaloacetato em fosfoenolpiruvato e dióxido de carbono. | |||
| description / en | description / en | ||
This refers a deficiency enzyme which in humans is encoded by the PCK1 gene. This is an enzyme in the lyase family used in the metabolic pathway of gluconeogenesis. It converts oxaloacetate into phosphoenolpyruvate and carbon dioxide. | |||
Revision as of 16:28, 16 August 2026
This refers a deficiency enzyme which in humans is encoded by the PCK1 gene. This is an enzyme in the lyase family used in the metabolic pathway of gluconeogenesis. It converts oxaloacetate into phosphoenolpyruvate and carbon dioxide.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_671802176 |
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| English | Phosphoenolpyruvate carboxykinase 1 deficiency |
This refers a deficiency enzyme which in humans is encoded by the PCK1 gene. This is an enzyme in the lyase family used in the metabolic pathway of gluconeogenesis. It converts oxaloacetate into phosphoenolpyruvate and carbon dioxide. |
