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Syntaxin 3
Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia
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Syntaxin 3, also known as STX3, is a protein[5] which in humans is encoded by the STX3 gene.[6][7]
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Function
The protein encoded by this gene is a member of the syntaxin family of cellular receptors for transport vesicles which participate in exocytosis in neutrophils.[6] STX3 has an important role in the growth of neurites and serves as a direct target for omega-6 arachidonic acid.[8] Mutations in Syntaxin 3 cause Microvillus inclusion disease.[9]
Interactions
Syntaxin 3 has been shown to interact with SNAP-25,[10][11][12] SNAP23[11][12][13][14] and SNAP29.[12]
References
Further reading
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