Humans normally have 46 chromosomes in each cell, divided into 23 pairs. Two copies of chromosome 17, one copy inherited from each parent, form one of the pairs. Chromosome 17 spans about 83 million DNA building blocks (base pairs) and represents between 2.5 and 3 percent of the total DNA in cells.
Identifying the 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 17 likely contains 1,100 to 1,200 genes that provide instructions for making proteins. These proteins perform a variety of different roles in the body.
Related Genetics Topics
- Charcot-Marie-Tooth disease — MedlinePlus Genetics
- Smith-Magenis syndrome — MedlinePlus Genetics
- Miller-Dieker syndrome — MedlinePlus Genetics
- Koolen-de Vries syndrome — MedlinePlus Genetics
- Acute promyelocytic leukemia — MedlinePlus Genetics
- Dermatofibrosarcoma protuberans — MedlinePlus Genetics
- 17q12 deletion syndrome — MedlinePlus Genetics
- 17q12 duplication — MedlinePlus Genetics
- Potocki-Lupski syndrome — MedlinePlus Genetics
- Yuan-Harel-Lupski syndrome — MedlinePlus Genetics
Source: MedlinePlus Genetics, U.S. National Library of Medicine.
