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