Full length protein corresponding to Human KCTD6 aa 1-237.Sequence: MDNGDWGYMMTDPVTLNVGGHLYTTSLTTLTRYPDSMLGAMFGGDFPTAR DPQGNYFIDRDGPLFRYVLNFLRTSELTLPLDFKEFDLLRKEADFYQIEP LIQCLNDPKPLYPMDTFEEVVELSSTRKLSKYSNPVAVIITQLTITTKVH SLLEGISNYFTKWNKHMMDTRDCQVSFTFGPCDY
KCTD6 (potassium channel tetramerization domain containing 6) is a protein-coding gene. Diseases associated with KCTD6 include maturity-onset diabetes of the young, and medulloblastoma, and among its related super-pathways are Melatonin Signaling and Activation of cAMP-Dependent PKA. An important paralog of this gene is KCTD1.
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