Chromosome 17

Chromosome 17 is a chromosome in the human genome. It is composed of more than 80 million base pairs and contains about 2,400 genes. It plays an important role in a wide array of biological processes, such as growth and differentiation, immune system regulation, and even the development of certain types of cancer. Chromosome 17 is associated with a number of diseases and genetic disorders, including Alzheimer’s, schizophrenia, Phelan-McDermid Syndrome, and several forms of cancer. Genes located on this chromosome are being actively researched in order to better understand their functions and how they may influence the development and progression of particular diseases. This knowledge can be used to develop more effective diagnostics and treatments for these conditions, as well as to gain new insights into the underlying causes of certain diseases.

← Journal of Chromosomes

Related Articles

6 article(s) found

Pericentric Inversion in Chromosome 10 in a Girl, Inherited from a Phenotypically Normal Mother: Case Report and Literature Review

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Humans Chromosome 1 Fractal Periods Signature is Highly Correlated with Intelligence and Brain Evolution

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Intriguing Humans and Primates chromosomes 4

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An Inherited Balanced Translocation Between Chromosomes 4 and 6 in Recurrent Pregnancy Loss: A Case Report

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A Patient with Monoclonal Gammopathy of Undetermined Significance and Detected Philadelphia Chromosome

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The Chromosomes of Dictyostelium Giganteum

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