7plp
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Structural highlights
DiseaseTEN4_HUMAN NON RARE IN EUROPE: Hereditary essential tremor. The disease is caused by variants affecting the gene represented in this entry. FunctionTEN4_HUMAN Involved in neural development, regulating the establishment of proper connectivity within the nervous system. Plays a role in the establishment of the anterior-posterior axis during gastrulation. Regulates the differentiation and cellular process formation of oligodendrocytes and myelination of small-diameter axons in the central nervous system (CNS) (PubMed:26188006). Promotes activation of focal adhesion kinase. May function as a cellular signal transducer (By similarity).[UniProtKB:Q3UHK6][1] References
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This page was last modified 07:52, 1 May 2024.