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The X chromosome is one of the two sex chromosomes in many organisms, including mammals, and is found in both males and females. It is a part of the XY sex-determination system and XO sex-determination system .
In this process, an X chromosome and a Y chromosome act to determine the sex of offspring, often due to genes located on the Y chromosome that code for maleness. Offspring have two sex chromosomes: an offspring with two X chromosomes (XX) will develop female characteristics, and an offspring with an X and a Y chromosome (XY) will develop male ...
The X chromosome is part of chromosome group C, and the Y chromosome is part of group G. Bands and sub-bands are annotated to the right of each chromosome (or chromosome pair), and the gene for the sex-determining region Y protein is located at Yp11.2.
The X and Y sex chromosomes are different in shape and size from each other, unlike the rest of the chromosomes , and are sometimes called allosomes. In some species, such as humans, organisms remain sex indifferent for a time during development ( embryogenesis ); in others, however, such as fruit flies, sexual differentiation occurs as soon as ...
Chromosomal sex is determined at the time of fertilization; a chromosome from the sperm cell, either X or Y, fuses with the X chromosome in the egg cell. Gonadal sex refers to the gonads, that is the testicles or ovaries, depending on which genes are expressed. Phenotypic sex refers to the structures of the external and internal genitalia. [6]
The cells of those born male contain an X chromosome and a Y chromosome that make a pair and give instructions on which genes should be expressed in the body, the researchers said.
The XO sex-determination system (sometimes referred to as X0 sex-determination system) is a system that some species of insects, arachnids, and mammals use to determine the sex of offspring. In this system, there is only one sex chromosome, referred to as X. Males only have one X chromosome (XO), while females have two
XX male syndrome, also known as de la Chapelle syndrome, is a rare intersex condition in which an individual with a 46,XX karyotype develops a male phenotype. [2] Synonyms for XX male syndrome include 46,XX testicular difference of sex development (or 46,XX DSD) [3] [4] [5] [6]