Chromosome 20 (human)

From Psychology Wiki

Chromosome 20 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 20 spans more than 63 million base pairs (the building material of DNA) and represents between 2 and 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 20 likely contains between 600 and 800 genes.

[edit] Genes

The following are some of the genes located on chromosome 20:

• EDN3: endothelin 3
• JAG1: jagged 1 (Alagille syndrome)
• PANK2: pantothenate kinase 2 (Hallervorden-Spatz syndrome)
• PRNP: prion protein (p27-30) (Creutzfeld-Jakob disease, Gerstmann-Strausler-Scheinker syndrome, fatal familial insomnia)

[edit] Diseases

The following diseases are some of those related to genes on chromosome 20:

• Alagille syndrome
• Maturity onset diabetes of the young type 1
• pantothenate kinase-associated neurodegeneration
• prion disease
• Waardenburg syndrome

[edit] References

• Deloukas, P. et al (2001). The DNA sequence and comparative analysis of human chromosome 20. Nature 414 (6866): 865-71. PMID 11780052.
• Gilbert, F. (1997). Disease genes and chromosomes: disease maps of the human genome. Genet Test 1 (3): 225-9. PMID 10464650.

This page uses content from the English-language version of Wikipedia. The original article was at Chromosome 20 (human). The list of authors can be seen in the page history. As with Psychology Wiki, the text of Wikipedia is available under the GNU Free Documentation License.