| Gene Symbol | FTH1 |
| Full Name | Ferritin Heavy Chain 1 |
| Chromosome | 19q13.33 |
| Protein Family | Ferritin heavy chain subunit |
| Function | is a hallmark of multiple neurodegenerative diseases including Alzheimer's disease (AD), Parkinson's disease (PD), and amyotrophic lateral sclerosis (ALS)[@ward2014]. |
| Molecular Weight | 21 kDa |
| Exons | 4 |
| Pathways | Apoptosis, Blood-Brain Barrier, Ferroptosis, Metastasis, Mitophagy |
| UniProt ID | P02794 |
| NCBI Gene ID | 2495 |
| Ensembl ID | ENSG00000196950 |
| OMIM | 134790 |
| GeneCards | FTH1 |
| Human Protein Atlas | FTH1 |
| Ferroxidase center | Located in FTH1, catalyzes Fe²⁺ → Fe³⁺ oxidation |
| Associated Diseases | ALS, Carcinoma, Hepatocellular Carcinoma, Parkinson's disease, Tumor, stroke |
| Known Drugs/Compounds | paricalcitol, dimethyl malonate |
| Interactions | GPX4, SIRT1, BECLIN1, NCOA4, UBE2N, TAK1 |
| KG Connections | 324 knowledge graph edges |
| Databases | GeneCardsHPASTRING |