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SEPT2

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

SEPT2
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Septin 2, also known as SEPT2, is a protein which in humans is encoded by the SEPT2 gene.[4][5]

Quick Facts SEPTIN2, Available structures ...
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Function

SEPT2 can hetero-oligomerize with SEPT6 and SEPT7 to form filaments.[6] SEPT2 interacted with SEPT6 through its C-terminal coiled-coil domain.[6] Knockdown of SEPT2, SEPT6, and SEPT7 in causes actin stress fibers to disintegrate and cells to lose polarity. Septins, SOCS7, and NCK1 are part of a signaling pathway that ties regulation of the DNA damage response to the cytoskeleton.[7]

Interactions

SEPT2 has been shown to interact with:

References

Further reading

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