DNA or genens these are the segments of the chromosome.
Genes on the Y chromosome are responsible for male sex determination and other male-specific traits. They play a crucial role in the development of male reproductive organs and secondary sexual characteristics.
The shorter sex chromosome in humans is the Y chromosome. It is responsible for determining male sex characteristics and only males have one copy, while females have two X chromosomes.
The allele that is responsible of Fabry Disorder/Disease is located on the X chromosome and is the only lipid storage disorder identified as being sex linked.
There are normally two copies of chromosome 7 in the nucleus of each human cell, one inherited from each parent. This makes a total of 2 chromosome 7.
DNA or genens these are the segments of the chromosome.
The most well characterized genes include DCX on the X chromosome, responsible for double cortex syndrome, and LIS1 on chromosome 17, the first gene identified for lissencephaly.
The pseudoautosomal regions (PARs) at the tips of the Y chromosome are homologous to regions on the X chromosome. These PARs are responsible for pairing and recombination between the X and Y chromosomes during meiosis. About 5% of the Y chromosome is homologous to the X chromosome in humans.
Genes on the Y chromosome are responsible for male sex determination and other male-specific traits. They play a crucial role in the development of male reproductive organs and secondary sexual characteristics.
The shorter sex chromosome in humans is the Y chromosome. It is responsible for determining male sex characteristics and only males have one copy, while females have two X chromosomes.
The allele that is responsible of Fabry Disorder/Disease is located on the X chromosome and is the only lipid storage disorder identified as being sex linked.
There are normally two copies of chromosome 7 in the nucleus of each human cell, one inherited from each parent. This makes a total of 2 chromosome 7.
Many sex-linked genes are found on the X chromosome. More than 100 sex-linked genetic disorders have now been mapped to the X chromosome. The human Y chromosome is much smaller than the X chromosome and appears to contain only few genes.
The sex determination in humans is determined by the male parent through the presence of the X or Y chromosome in the sperm. The female parent always contributes an X chromosome. If the sperm carries an X chromosome, the resulting offspring will be female (XX), and if it carries a Y chromosome, the offspring will be male (XY).
No, each chromosome carries many genes that code for multiple characteristics or traits. Different genes on the same chromosome can be responsible for different traits, and some traits may be controlled by genes on different chromosomes.
Chromosome 22 is one of the 23 pairs of chromosomes in humans, carrying genetic information and responsible for determining various traits. It is the second smallest human chromosome, containing around 50-60 million base pairs and around 600-800 genes. Mutations or abnormalities in chromosome 22 can lead to genetic disorders such as DiGeorge syndrome or velocardiofacial syndrome.
We have no dinosaur DNA samples to study. Hence, we cannot determine which chromosomes were responsible for a dinosaur's color.