| 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.