翻訳と辞書
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・ Chromosomal polymorphism
・ Chromosomal rearrangement
・ Chromosomal translocation
・ Chromosome
・ Chromosome (genetic algorithm)
・ Chromosome 1 (human)
・ Chromosome 10 (human)
・ Chromosome 11 (human)
・ Chromosome 12 (human)
・ Chromosome 13 (human)
・ Chromosome 14 (human)
・ Chromosome 15 (human)
・ Chromosome 15q partial deletion
・ Chromosome 15q trisomy
・ Chromosome 16 (human)
Chromosome 16 open reading frame 13
・ Chromosome 17 (human)
・ Chromosome 18 (human)
・ Chromosome 19 (human)
・ Chromosome 2 (human)
・ Chromosome 20 (human)
・ Chromosome 21 (human)
・ Chromosome 22 (human)
・ Chromosome 3 (human)
・ Chromosome 4 (human)
・ Chromosome 5 (human)
・ Chromosome 5q deletion syndrome
・ Chromosome 6 (human)
・ Chromosome 6 open reading frame 165
・ Chromosome 7 (human)


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Chromosome 16 open reading frame 13 : ウィキペディア英語版
Chromosome 16 open reading frame 13


Chromosome 16 open reading frame 13, also called C16orf13, is a protein-coding gene of unknown function, also known as ''JFP2''. Though the function of this gene is unknown, various data have revealed that it is expressed at high levels in various cancerous tissues. Underexpression of this gene has also been linked to disease consequences in humans.
== Gene ==

C16orf13 is located on the short arm of chromosome 16 in humans, in the thirteenth open reading frame. There are five transcript variants of this gene, named 1, 2, 3, 4, and 7. The longest cDNA transcript (transcript variant 1) contains 854 base pairs. This transcript is composed of six exons, all of which contribute to the major superfamily included in the protein, the (methyltransferases superfamily ). The primary transcript of this gene is 1,919 base pairs long.

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「Chromosome 16 open reading frame 13」の詳細全文を読む



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