7k3x
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SGMGCIT segment 58-64 from Keratin-8 with G62C mutation
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Structural highlights
DiseaseK2C8_HUMAN The disease is caused by variants affecting the gene represented in this entry. FunctionK2C8_HUMAN Together with KRT19, helps to link the contractile apparatus to dystrophin at the costameres of striated muscle.[1] References
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This page was last modified 07:17, 3 April 2024.