9g6d
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CLC7/OSTM1 complex in the absence of PIP2 lipid.
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Structural highlights
DiseaseOSTM1_HUMAN Infantile osteopetrosis with neuroaxonal dysplasia. The disease is caused by variants affecting the gene represented in this entry. FunctionOSTM1_HUMAN Required for osteoclast and melanocyte maturation and function.[1] References
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This page was last modified 05:37, 30 July 2025.