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NEET UG 2026 » NEET UG Study Material » Biology » Genetics
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Genetics

It is a sub-discipline of biology that is concerned with the research of heredity and its biological processes, the investigation of genes, the study of the genome, the cell cycle, the study of heredity, the inheritance of genes, and many other topics.

Table of Content
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Genetics is the study of the working and major codes of variation and heredity, as well as their interactions. The term “inheritance” refers to the foundation upon which heredity is built. As described by the dictionary, it is the process by which qualities are passed down from one generation to the next. He is renowned as “the Father of Modern Genetics” for his discoveries into the fundamental laws of heredity that he made throughout his lifetime.

By Gregor Mendel, he established the Law of Inheritance. The garden pea (Pisum Sativum) was the plant on which Mendel conducted his seven-year experimentation before coming to the conclusion that the rules of inheritance apply to living organisms. Mendel selected seven key traits of the Pisum Sativum plant for his studies on hybridization after conducting extensive research on the plant. Mendel employed true-breeding lines, which are lines that go through regular self-pollination and have a consistent level of distinctive heritance, in his research.

Mendel’s Laws of Inheritance 

The Fundamental Principles of Inheritance

Observing the monohybrid cross, Gregor Mendel postulated two laws of inheritance:

The Law of Dominance states that distinct elements, referred to as factors, determine the properties of a system. These two elements are present at all times as a pair. One of the couple’s constituent genes has a significant advantage over the other.

Segregation Law – Alleles do not mix, and the two features are retained throughout the gamete production process (in the F2 generation). The characters are distinct from one another and are passed on to different gametes. Homozygous generates gametes that are similar in appearance, while heterozygous produces gametes that are different in appearance and have different traits.

It is the discovery that was made after Mendel’s research was completed. Completive dominance is a genetic condition that occurs when both alleles do not express the same dominant trait, leading to an indistinguishable combination of traits or a midway between the features of the alleles.

Codominance

The combination of two alleles that do not have a dominant-recessive connection and so affect the creature as a whole.

The Law of Independent Assortment is a law that governs how things are arranged in a collection.

When two sets of characteristics are combined to form a hybrid, the separation of one set of characteristics is independent of the separation of the other set of characteristics.

When it comes to inheritance, the Chromosomal Theory is the most widely accepted.

Both genes and chromosomes are found in pairs, just as they are in pairs of two. The homologous chromosome contains the two alleles of a gene pair that are found in the homologous places on the parent chromosome. In the event that a set of chromosomes is coupled and then separated, this will result in a split in the set of genes (factors) that they carry. The Chromosomal Theory of Inheritance is the name given to this collection of knowledge.

Determination of a man’s sexual orientation

Henking had the impression that there was a certain nuclear configuration. He saw that this particular nuclear configuration was only found in fifty percent of sperms, which he thought was unusual. He referred to this particular body as x. Later, it was discovered that only ovules that have only the x chromosome are born female, whereas those that do not have this circumstance are born males. As a result, the X-chromosome became known as the sex chromosome, while the remaining chromosomes became known as autosomes.

Conclusion 

Children and their parents differ in terms of the level of dissimilarity that exists between them and their parents, as the name implies. It can be assessed by taking into consideration the behavioural, cytological, physiological, and morphological characteristics of individuals belonging to the same species as the one in question.

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Frequently asked questions

Get answers to the most common queries related to the NEET UG Examination Preparation.

What are the four different types of genes?

Ans: DNA is made up of millions of tiny molecules known as bases, which...Read full

Who has the most powerful genes? Is it better to be a mother or a father?

Ans: In terms of genetic makeup, you really have more of your mother...Read full

What causes blue eyes to be so uncommon?

Ans:  Due to the fact that blue eyes are genetically recessive, only 8...Read full

What are some of the genetics applications?

Ans: Medicine. Genetic approaches are used in medicine to diagnose and ...Read full

What is the total number of genes in a human being?

Ans:  It has been estimated that humans have between 20,000 and 25,000 genes, according to a collaborative m...Read full

Ans:

DNA is made up of millions of tiny molecules known as bases, which are found in every cell of the body. The compounds are available in four different types: A, C, T, and G. A gene is a segment of DNA that has a sequence of the letters A, C, T, and G. Your genes are so little that there are around 20,000 of them in each and every cell in your body!

Ans:

In terms of genetic makeup, you really have more of your mother’s genes than you have of your father’s. This is due to the mitochondria, which are little organelles that dwell within your cells and which you can only obtain from your mother during pregnancy.

Ans:

 Due to the fact that blue eyes are genetically recessive, only 8% of the world’s population is born with blue eyes. Despite the fact that blue eyes are substantially less prevalent than brown eyes throughout the world, they are particularly popular in nationalities that live near the Baltic Sea in northern Europe.

 

Ans:

Medicine. Genetic approaches are used in medicine to diagnose and treat inherited human illnesses that are passed down through families. Finding out whether or not you have a family history of diseases such as cancer or various disorders may indicate that you have a hereditary tendency to develop these ailments.

 

 

Ans:

 It has been estimated that humans have between 20,000 and 25,000 genes, according to a collaborative multinational research effort known as the Human Genome Project, which aimed to discover the sequence of the human genome and identify the genes that it contained. Every individual possesses two copies of each gene, one of which was inherited from each parent.

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