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・ 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)
・ Chromosome abnormality


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Chromosome 19 (human) : ウィキペディア英語版
Chromosome 19 (human)

Chromosome 19 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 19 spans more than 58.6 million base pairs, the building material of DNA.
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. Depending on the genome annotation used, chromosome 19 contains 2,188 or 2,670 genes, and chromosome 19 thereby has the highest gene density of all the 24 chromosomes.
==Genes==
The following are some of the genes located on chromosome 19:
* KLK3: The Prostate-specific antigen (PSA)
* NWD1: NACHT and WD repeat domain containing 1.
* PEX11G: peroxisomal biogenesis factor 11 gamma
* PRX: Periaxin
* SLC5A5: Solute carrier family 5 (sodium iodide symporter), member 5
* STK11: Serine/threonine kinase 11 (Peutz-Jeghers syndrome)
* ZNF649: Transcriptional suppressor

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