Familial apolipoprotein C-II deficiency (Q106757): Difference between revisions
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Trata-se de uma deficiência de uma proteína que, em humanos, é codificada pelo gene APOC2. A proteína codificada por este gene é secretada no plasma, onde é um componente de lipoproteínas de densidade muito baixa e quilomícrons. | |||
| description / en | description / en | ||
This is a deficiency in a protein that in humans is encoded by the APOC2 gene. The protein encoded by this gene is secreted in plasma where it is a component of very low density lipoproteins and chylomicrons. | |||
Revision as of 13:45, 17 August 2026
This is a deficiency in a protein that in humans is encoded by the APOC2 gene. The protein encoded by this gene is secreted in plasma where it is a component of very low density lipoproteins and chylomicrons.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_877401371 |
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| English | Familial apolipoprotein C-II deficiency |
This is a deficiency in a protein that in humans is encoded by the APOC2 gene. The protein encoded by this gene is secreted in plasma where it is a component of very low density lipoproteins and chylomicrons. |
