AP1S1
Lua error in Module:Infobox_gene at line 53: attempt to index field 'wikibase' (a nil value). AP-1 complex subunit sigma-1A is a protein that in humans is encoded by the AP1S1 gene.[1][2][3]
Function
[edit | edit source]The protein encoded by this gene is part of the clathrin coat assembly complex which links clathrin to receptors in coated vesicles. These vesicles are involved in endocytosis and Golgi processing. This protein, as well as beta-prime-adaptin, gamma-adaptin, and the medium (mu) chain AP47, form the AP-1 assembly protein complex located at the Golgi vesicle. Two alternatively spliced transcript variants of this gene, which encode distinct isoforms, have been reported.[3]
A mutation in the AP1S1 causes the rare familial MEDNIK syndrome described in 2008.[4]
Interactions
[edit | edit source]AP1S1 has been shown to interact with AP1G1[2][5][6] and RAB10.[7]
References
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Further reading
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External links
[edit | edit source]- Human AP1S1 genome location and AP1S1 gene details page in the UCSC Genome Browser.
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