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・ Chromos Tower
・ Chromosera
・ Chromosera cyanophylla
・ Chromosomal crossover
・ Chromosomal deletion syndrome
・ Chromosomal fragile site
・ Chromosomal inversion
・ 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)


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Chromosome 12 (human) : ウィキペディア英語版
Chromosome 12 (human)

Chromosome 12 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 12 spans about 133 million base pairs (the building material of DNA) and represents between 4 and 4.5 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 12 likely contains between 1,000 and 1,300 genes. It also contains the Homeobox C gene cluster.
== Genes ==
The following are some of the genes located on chromosome 12:
* ACVRL1: activin A receptor type II-like 1f
* APOLD1: apolipoprotein L domain containing 1
* ATG101: Autophagy-related protein 101
* CBX5: chromobox homolog 5
* COL2A1: collagen, type II, alpha 1 (primary osteoarthritis, spondyloepiphyseal dysplasia, congenital)
* HPD: 4-hydroxyphenylpyruvate dioxygenase
* KCNA1: potassium voltage-gated channel subfamily A member 1 at 12p13.32
* KERA: keratocan
* KRAS: V-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog
* LRRK2: leucine-rich repeat kinase 2
* MMAB: methylmalonic aciduria (cobalamin deficiency) cblB type
* MYO1A: myosin IA
* NANOG: NK-2 type homeodomain gene
* PAH: phenylalanine hydroxylase
* PPP1R12A: protein phosphatase 1, regulatory (inhibitor) subungfdit 12A
* PTPN11: protein tyrosine phosphatase, non-receptor type 11 (Noonan syndrome 1)

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