In humans it would be the X chromosome.
Sex-linked disorders are caused by genes located on the sex chromosomes, particularly the X chromosome. Since males have only one X chromosome, mutations in genes on this chromosome are more likely to be expressed in males compared to females who have two X chromosomes. This is why sex-linked disorders are more commonly seen in males.
males have only one X chromosomes
Prokaryotic chromosomes are simpler and circular, found in the cytoplasm, while eukaryotic chromosomes are more complex and linear, found in the nucleus. Eukaryotic chromosomes are organized with histone proteins into chromatin, while prokaryotic chromosomes lack histones.
Combined chromosomes are often referred to as "chromosomal fusions" or "fusion chromosomes." This occurs when two or more chromosomes merge together, which can happen naturally or through genetic manipulation. In some instances, such as in certain cancers or genetic disorders, these fusions can lead to abnormal cell behavior and disease.
Sex-linked disorders are inherited through genes located on the sex chromosomes (X and Y). Diseases on the X chromosome are more common because males have only one X chromosome, making them more susceptible to X-linked disorders. Females have two X chromosomes, offering a protective factor where a mutation on one X chromosome may be compensated by the other. Y-linked disorders are rare and only affect males since females do not have a Y chromosome.
DNA is found in the nucleus of eukaryotic cells, where it is tightly packaged into chromosomes. In prokaryotic cells, DNA is found in the nucleoid region, a less organized structure than eukaryotic chromosomes.
Sex-linked disorders are genetic conditions that are linked to the sex chromosomes, typically the X chromosome. These disorders are more commonly seen in males because they only have one X chromosome. Females have two X chromosomes, which can sometimes compensate for the effects of the disorder. Sex-linked disorders can affect individuals by causing a range of symptoms and health issues, such as color blindness, hemophilia, and Duchenne muscular dystrophy. These disorders can impact a person's quality of life and may require ongoing medical management.
no, normally humans do have 46, but certain mutations or genetic disorders can result in more, less, or fused chromosomes. the most common example of missing chromosomes is down's syndrome. when someone has an extra chromosome(s) it's called polyploidy. i can't tell you too much about fused chromosomes.
Autosomal disorders generally have a greater impact on a person's health compared to sex chromosome disorders. This is because autosomal chromosomes carry a wider range of genes that influence various bodily functions and traits, and many autosomal disorders can lead to severe developmental and health issues, such as Down syndrome or cystic fibrosis. In contrast, sex chromosome disorders, like Turner syndrome or Klinefelter syndrome, often have more specific effects and may not be as universally debilitating.
Eukaryotic cells, such as those found in plants, animals, and fungi, have more chromosomes and genes than bacteria. Eukaryotic cells typically have multiple linear chromosomes and a more complex genome organization compared to the single circular chromosome of bacteria.
Autosomes come in pairs usually (one from the mother, and one from the father), but, sometimes, as in with genetic disorders, you might find things like trisomies, where you have 3 chromosomes for the same autosome, or monosomies, where you only have 1 instead of two.
During cell reproduction, chromosomes condense from the chromatin that is normally found in the nucleus. Condensation helps the chromosomes become more manageable and facilitates their movement during processes such as mitosis and meiosis. After cell division is complete, the condensed chromosomes will decondense back into chromatin.