New page: ==hEAG PAS domain== <StructureSection load='5j7e' size='340' side='right' caption='5j7e, resolution 1.90Å' scene=''> == Structural highlights == <table><tr><td co... |
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Structural highlights
Disease[KCNH1_HUMAN] The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. Function[KCNH1_HUMAN] Pore-forming (alpha) subunit of a voltage-gated delayed rectifier potassium channel (PubMed:22732247). Channel properties may be modulated by subunit assembly, but not by cyclic nucleotides (By similarity). Mediates IK(NI) current in myoblasts (PubMed:9738473). Involved in the regulation of cell proliferation and differentiation, in particular adipogenic and osteogenic differentiation in bone marrow-derived mesenchymal stem cells (MSCs) (PubMed:23881642).[UniProtKB:Q60603][1] [2] [3] References
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This page was last modified 19:48, 13 May 2016.