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In humans and many other species of animals, the father determines the sex of the child. In the XY sex-determination system, the female-provided ovum contributes an X chromosome and the male-provided sperm contributes either an X chromosome or a Y chromosome, resulting in female (XX) or male (XY) offspring, respectively.
Sex chromosomes (also referred to as allosomes, heterotypical chromosome, gonosomes, heterochromosomes, [1] [2] or idiochromosomes [1]) are chromosomes that carry the genes that determine the sex of an individual. The human sex chromosomes are a typical pair of mammal allosomes. They differ from autosomes in form, size, and behavior.
Most mammals, including humans, have an XY sex-determination system: the Y chromosome carries factors responsible for triggering male development. In the absence of a Y chromosome, the fetus will undergo female development. This is because of the presence of the sex-determining region of the Y chromosome, also known as the SRY gene. [5]
There are two kinds of sex chromosomes–X and Y. In humans and in almost all other mammals, females carry two X chromosomes, designated XX, and males carry one X and one Y, designated XY. [1] A human egg contains only one set of chromosomes (23) and is a haploid. Sperm also have only one set of 23 chromosomes and are therefore haploid.
However, when an extra DAX1 gene is placed on the X chromosome, the result is a female, despite the existence of SRY, since it overrides the effects of SRY. [11] Even when there are normal sex chromosomes in XX females, duplication or expression of SOX9 causes testes to develop.
In 2021, scientists reported sequencing a complete, female genome (i.e., without the Y chromosome). [4] [3] The human Y chromosome, consisting of 62,460,029 base pairs from a different cell line and found in all males, was sequenced completely in January 2022. [5] The current version of the standard reference genome is called GRCh38.p14 (July ...
Sex differences in human physiology are distinctions of physiological characteristics associated with either male or female humans. These can be of several types, including direct and indirect, direct being the direct result of differences prescribed by the Y-chromosome (due to the SRY gene ), and indirect being characteristics influenced ...
46,XX/46,XY chimeric or mosaic is associated with a wide spectrum of different physical presentations, with cases ranging from having a completely normal male or female phenotype [7] [8] [9] to some cases having ovotesticular syndrome. Due to this variation, genetic testing is the only way to reliably make a diagnosis.