the genes are in the egg. so the women who gave the egg will share the genes of the baby
Each part of the embryo holds different characteristics and genes such as hair and eye color. The location of these genes determine what it is specified for.
Genes control the sex of a developing embryo.
The series of genes that control the development of organs and tissues in the embryo is known as the Hox genes. These genes play a crucial role in determining the body plan and the positioning of body parts during embryonic development.
An embryo inherits a full set of genes through the combination of genetic material from both the egg and sperm during fertilization. Each parent contributes half of their genetic material, resulting in a complete set of genes in the embryo.
Homeobox genes are a series of genes that control the embryonic development of organs and tissues in various parts of the embryo. These genes regulate the formation and positioning of structures in the developing organism. Deregulation of homeobox genes can lead to developmental abnormalities.
LAC gene
Genes inherited from both the mother and father influence embryo development by determining traits such as physical characteristics, health, and behavior. These genes provide the instructions for how cells grow and function, ultimately shaping the development of the embryo into a fully formed individual.
Hox gene mutation can change the organs that develop in specific parts of an embryo. These genes play a crucial role in determining the body plan and segment identity during development. Mutations in Hox genes can disrupt this process, leading to abnormal organ development in specific regions of the embryo.
Mutations in the lac genes can lead to changes in the development of organs in specific regions of an embryo. These mutations can alter the expression of lac genes, which are involved in controlling the development of certain tissues and organs. As a result, the normal process of organ development in those specific regions can be disrupted, leading to abnormalities or different organ structures.
An embryo is not always stimulated to develop into a female. The presence of the Y chromosome leads to the development of a male embryo through the expression of genes that promote male characteristics. In the absence of the Y chromosome, the default pathway is for the embryo to develop into a female.
Proteins do not directly control the sex of a developing embryo. The sex of an embryo is determined by the combination of sex chromosomes inherited from the parents. In mammals, the presence of a Y chromosome typically leads to the development of a male, while its absence results in a female.
Another word for genes is "genetic material" or "DNA."