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Literature summary for 2.3.1.255 extracted from
- Naa10 in development and disease (2015), Oncotarget, 6, 34041-34042.
Protein Variants
| Protein Variants | Comment | Organism |
|---|---|---|
| S37P | the mutation is the cause of Ogden Syndrome | Homo sapiens |
Localization
| Localization | Comment | Organism | GeneOntology No. | Textmining |
|---|---|---|---|---|
| ribosome | - |
Homo sapiens | 5840 | - |
Organism
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Homo sapiens | P41227 | - |
- |
Synonyms
| Synonyms | Comment | Organism |
|---|---|---|
| NAA10 | - |
Homo sapiens |
General Information
| General Information | Comment | Organism |
|---|---|---|
| malfunction | mutations in N-terminal acetyltransferase Naa10 are the cause of Ogden Syndrome | Homo sapiens |
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Release 2023.1 (January 2023)
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