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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.
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.
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]
The XY sex-determination system is a sex-determination system present in many mammals, including humans, some insects (Drosophila), some snakes, some fish (guppies), and some plants (Ginkgo tree). In this system, the sex of an individual usually is determined by a pair of sex chromosomes. Typically, females have two of the same kind of sex ...
Sex-determination system. Some chromosomal sex determination systems in animals. A sex-determination system is a biological system that determines the development of sexual characteristics in an organism. [1] Most organisms that create their offspring using sexual reproduction have two common sexes and a few less common intersex variations.
Karyotype. A karyotype is the general appearance of the complete set of chromosomes in the cells of a species or in an individual organism, mainly including their sizes, numbers, and shapes. [1][2] Karyotyping is the process by which a karyotype is discerned by determining the chromosome complement of an individual, including the number of ...
The human genome is a complete set of nucleic acid sequences for humans, encoded as the DNA within each of the 24 distinct chromosomes in the cell nucleus. A small DNA molecule is found within individual mitochondria. These are usually treated separately as the nuclear genome and the mitochondrial genome. [1]
This is an accepted version of this page This is the latest accepted revision, reviewed on 4 November 2024. DNA molecule containing genetic material of a cell This article is about the DNA molecule. For the genetic algorithm, see Chromosome (genetic algorithm). Chromosome (10 7 - 10 10 bp) DNA Gene (10 3 - 10 6 bp) Function A chromosome and its packaged long strand of DNA unraveled. The DNA's ...