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Tubulin beta-4A chain is a protein that in humans is encoded by the ''TUBB4A'' gene. Two tubulin beta-4 chain proteins are encoded in the human genome by the genes TUBB4A (this entry) and TUBB4B.〔(【引用サイトリンク】 url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10382 )〕 Tubulin is the major constituent of microtubules, a key components of the cytoskeleton. It binds two moles of GTP, one at an exchangeable site on the beta-chain and one at a non-exchangeable site on the alpha-chain. ''TUBB4A'' is preferentially and highly expressed in the central nervous system. == Clinical signficance == Mutations in TUBB4A have been associated with two neurological disorders. An R2G substitution in the autoregulatory MREI domain of TUBB4A has been identified as the cause of 'hereditary whispering dysphonia' or DYT4. A ''de novo'' D249N mutation has been identified as the cause of a rare leukoencephalopathy, hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC). Mutations in TUBB4A are associated to . 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Tubulin beta-4A chain」の詳細全文を読む スポンサード リンク
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