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Sialin : ウィキペディア英語版
SLC17A5

Solute carrier family 17 (anion/sugar transporter), member 5, also known as SLC17A5 or sialin, is a protein which in humans is encoded by the ''SLC17A5'' gene.〔(【引用サイトリンク】 url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=26503 )
== Clinical significance ==

A deficiency of this protein causes Salla disease.〔
The gene for HP59 contains, entirely within its coding region, the Sialin Gene SLC17A5. Member 5, also known as SLC17A5 or sialin is a lysosomal membrane sialic acid transport protein which in humans is encoded by the SLC17A5 gene on Chromosome 6〔http://www.ncbi.nlm.nih.gov/nuccore/224514687?report=graph&from=12483827&to=12483911〕〔()"Entrez Gene: SLC17A5 solute carrier family 17 (anion/sugar transporter), member 5"〕

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「SLC17A5」の詳細全文を読む



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