| SQSTM1 |
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| Identifiers |
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| Aliases | SQSTM1, A170, OSIL, PDB3, ZIP3, p60, p62, p62B, FTDALS3, Sequestosome 1, NADGP, DMRV |
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| External IDs | OMIM: 601530; MGI: 107931; HomoloGene: 31202; GeneCards: SQSTM1; OMA:SQSTM1 - orthologs |
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| Gene location (Mouse) |
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| | Chr. | Chromosome 11 (mouse) |
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| | Band | 11|11 B1.3 | Start | 50,090,193 bp |
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| End | 50,101,654 bp |
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| RNA expression pattern |
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| Bgee | | Human | Mouse (ortholog) |
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| Top expressed in | - right adrenal cortex
- left adrenal gland
- left adrenal cortex
- stromal cell of endometrium
- muscle of thigh
- right lobe of thyroid gland
- left lobe of thyroid gland
- gallbladder
- gastric mucosa
- Descending thoracic aorta
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| | Top expressed in | - dentate gyrus of hippocampal formation granule cell
- muscle of thigh
- right kidney
- triceps brachii muscle
- adrenal gland
- ventromedial nucleus
- superior frontal gyrus
- temporal muscle
- central gray substance of midbrain
- sternocleidomastoid muscle
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| | More reference expression data |
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| BioGPS | |
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| Wikidata |
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Sequestosome-1 is a protein that in humans is encoded by the SQSTM1 gene. Also known as the ubiquitin-binding protein p62, it is an autophagosome cargo protein that targets other proteins that bind to it for selective autophagy. By interacting with GATA4 and targeting it for degradation, it can inhibit GATA-4 associated senescence and senescence-associated secretory phenotype.
Mutations in SQSTM1 are a common cause of Paget's disease of bone.