7cq5
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Structure of the human CLCN7-OSTM1 complex with ATP
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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] See AlsoReferences
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This page was last modified 09:28, 9 April 2025.