| Gene Symbol | ATG16L1 |
| Chromosome | 2q37.1 |
| Function | is a core autophagy protein essential for autophagosome formation and cellular protein quality control. |
| Primary Expression | neurons and glial cells throughout the brain, including the cortex, [hippocam |
| Subcellular Localization | </th><td>Autophagosome membrane, Cytoplasm</td></tr> |
| Amino Acids | 607 aa |
| Pathways | Akt, Autophagy, Epigenetic, Mapk, Mtor |
| Ensembl ID | ENSG00000085978 |
| GeneCards | ATG16L1 |
| Human Protein Atlas | ATG16L1 |
| Coiled-Coil Domain (residues 150–300) | Important for homodimerization of ATG16L1. The dimerized form creates a multivalent platform that enhances ATG5 binding. |
| Mitophagy | ATG16L1 helps target damaged mitochondria for autophagic degradation through interactions with autophagy receptors like p62/SQSTM1 and OPTN. |
| Aggrephagy | The protein participates in the clearance of protein aggregates, which is particularly important in neurodegenerative diseases. |
| Xenophagy | ATG16L1 contributes to the degradation of intracellular pathogens. |
| Synaptic Protein Turnover | Autophagy regulates synaptic protein composition and function at presynaptic and postsynaptic terminals. |
| Associated Diseases | Inflammation, Intestinal Disease, Osteoarthritis, Parkinson, Rheumatoid Arthritis, Tumor |
| Known Drugs/Compounds | rapamycin |
| Interactions | ABP, AIM2, AKT, AKT1, ALZHEIMER, ALZHEIMER'S DISEASE |
| KG Connections | 565 knowledge graph edges |
| Databases | GeneCardsUniProtNCBI GeneHPASTRING |
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