| Gene Symbol | NMNAT1 |
| Full Name | Nicotinamide Mononucleotide Adenylyltransferase 1 |
| Chromosome | 1p36.22 |
| Protein Type | Enzyme |
| Function | encodes a crucial enzyme in NAD+ biosynthesis that catalyzes the final step in the NAD+ salvage pathway: the conversion of nicotinamide mononucleotide (NMN) to nicotinamide adenine dinucleotide (NA... |
| Primary Expression | tissues with high metabolic demand |
| Subcellular Localization | s and tissue expression patterns. While NMNAT1 is primarily studied in the context of Leber congenital amaurosis (LCA) |
| Molecular Weight | 32 kDa |
| Amino Acids | 279 aa |
| Exons | 13 |
| UniProt ID | [Q9PVN7](https://www.uniprot.org/uniprot/Q9PVN7) |
| Ensembl ID | ENSG00000160714 |
| OMIM | 608709 |
| GeneCards | NMNAT1 |
| Human Protein Atlas | NMNAT1 |
| Associated Diseases | neurodegeneration |
| Interactions | ALZHEIMER, ALZHEIMER'S DISEASE, AXON, Caspase, CASPASE-3, NAD |
| KG Connections | 24 knowledge graph edges |
| Databases | GeneCardsNCBI GeneHPASTRING |
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