翻訳と辞書
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・ 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)
・ Chromosome 8 (human)
・ Chromosome 9 (human)


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Chromosome 18 (human) : ウィキペディア英語版
Chromosome 18 (human)

Chromosome 18 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 18 spans about 80 million base pairs (the building material of DNA) and represents about 2.5 percent of the total DNA in cells.
Identifying genes on each chromosome is an active area of genetic research. Because researchers use different approaches to predict the number of genes on each chromosome, the estimated number of genes varies. Chromosome 18 likely contains between 300 and 400 genes.
==Genes==
The following are some of the genes located in chromosome 18:
* DCC: Deleted in Colorectal Cancer
* FECH: ferrochelatase (protoporphyria)
* NPC1: Niemann-Pick disease, type C1
* SMAD4: SMAD, mothers against DPP homolog 4 (Drosophila)
* KC6: Keratoconus gene 6, discovery reported in 2005;

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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