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No, both members of a homologous pair are not inherited from the same parent. One member of each homologous pair comes from the mother, and the other comes from the father. This pairing occurs during sexual reproduction, where each parent contributes one chromosome to form a homologous pair in the offspring.

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A cell that contains both sets of Homologous chromosomes said to be what?

A cell that contains both sets of homologous chromosomes is said to be diploid. In diploid cells, one set of chromosomes is inherited from each parent, allowing for genetic diversity. This is typically the case in somatic cells of multicellular organisms, while gametes (sperm and egg cells) are haploid, containing only one set of chromosomes.


What are the Members of a gene pairs are identical?

When the members of a gene pair are identical, the organism is described as homozygous for that trait. This means both alleles, one inherited from each parent, are the same, whether they are dominant or recessive. Homozygosity can influence the expression of traits, as both alleles will produce the same phenotype. In contrast, if the alleles are different, the organism is heterozygous.


Can you look like both of your parents?

Yes, a child can have a mix of physical traits from both parents, such as eye color, hair color, and facial features. This combination is determined by the genes inherited from each parent.


In humans alleles for each gene are inherited from?

In humans, alleles for each gene are inherited from both parents, with each parent contributing one allele for each gene. This means that individuals have two alleles for each gene, one inherited from the mother and one from the father. The combination of these alleles determines the individual's traits and characteristics.


Is homologous chromosomes only present in cells that undergo meiosis?

Usually they dont as homologous chromosomes form bivalents with other homologous chromosomes and crossing over occurs between the 2. But if a chiasmata does form between the t homologous chromosomes they can change information.

Related Questions

What phenotype produces is between the two homologous parents?

The phenotype that is a combination of traits from both homologous parents is called the composite phenotype. It results from the interaction of different alleles inherited from each parent. This can lead to a unique expression of characteristics not seen in either parent.


What is the significance of the members of a homologous pair of chromosomes in genetic inheritance?

The members of a homologous pair of chromosomes are important in genetic inheritance because they carry similar genes, one from each parent. During meiosis, these chromosomes exchange genetic material through crossing over, leading to genetic variation in offspring. This process ensures that each individual has a unique combination of genetic traits inherited from both parents.


Why can't we inherit both copies of a homologous chromosome from the same parent?

If we inherited both copies of a homologous chromosome, that would mean that we would only have one parent. Since mammals reproduce by sexual reproduction, it is impossible for this to happen.


A cell that contains both sets of Homologous chromosomes said to be what?

A cell that contains both sets of homologous chromosomes is said to be diploid. In diploid cells, one set of chromosomes is inherited from each parent, allowing for genetic diversity. This is typically the case in somatic cells of multicellular organisms, while gametes (sperm and egg cells) are haploid, containing only one set of chromosomes.


What are chromosomes that contain genes which code for the same traits?

Homologous chromosomes are chromosomes that contain genes that code for the same traits, one inherited from each parent. These chromosomes carry similar genetic information, such as eye color or hair type, and are crucial for genetic diversity and inheritance in offspring.


What are the Members of a gene pairs are identical?

When the members of a gene pair are identical, the organism is described as homozygous for that trait. This means both alleles, one inherited from each parent, are the same, whether they are dominant or recessive. Homozygosity can influence the expression of traits, as both alleles will produce the same phenotype. In contrast, if the alleles are different, the organism is heterozygous.


Where the alleles for given trait are inherited from?

The alleles for a given trait are inherited from an individual's parents.


Are homologous chromosomes present in both mitosis and meiosis?

Yes, homologous chromosomes are present in both mitosis and meiosis. In mitosis, homologous chromosomes do not pair up, while in meiosis, homologous chromosomes pair up during prophase I.


What are homologous choromosomes?

Homologous chromosomes are pairs of each other. They are chromosomes that are identical to each other except for a few variations. Everybody has one from their mom and dad. Everybody has 46 chromosomes, but in reality it is less confusing to say "we have 23 pairs of chromosomes."


How is Treacher Collins Syndrome passed from parent to offspring?

This syndrome is caused by a new mutation in one or two genes in 60% of the cases. These are not inherited. The other 20% are inherited if one parent carries the mutated gene. In the final 20% both parents have to carry a different gene for their offspring to have the syndrome. In this case neither parent show any signs or symptoms.


What is it when both genes are the same either both dominant or both recessive?

Homologous.


Can brother and sister one be A positive and one A negative?

Blood type is an inherited trait from both parents. If one parent were A- and the other A+. The kids can inherit either.