What is Heterozygous? What Does It Represent?

heterozygous In order to better understand what is and what it is talking about, first of all, it is necessary to understand the zygote. To briefly define the zygote, it is the name given to the cellular structure that is formed as a result of the fusion of two sex cells, one of which comes from the mother and the gluttonous father.

What is Heterozygous?

The zygote, which is the first step of the embryo, completes its development over time and divides to form the living thing.

Heterozygous is a type of zygote. As the name suggests, this type of zygote is formed by heterogeneity, that is, by the emergence of different genes or chromosomes. Heterozygous another namewith hybrid progenyIt contains both DNA (deoxyribose nucleic acid) and RNA (ribo nucleic acid) in its structure.

What is Heterozygous

What is MTHFR?

MTHFR mutations are thought to be at the root of many health issues. MTHFR, which stands for Methylene Tetra Hydro Folate Reductase, is actually both a type of gene and an enzyme. The most common mutation types in this gene are C677T and A1298C point mutations. What is Mthfr C667T heterozygous carrier In response to the question, it is necessary to examine the C677T. 677 in C677T indicates line 677 of the encoded gene. Here C stands for cytosine and T stands for thymine. The change of these genes is called the C677T mutation.

mthfr a1298c heterozygous

Similarly, mutation occurred in line 1298 of the gene in MTHFR A1298C. Due to these mutations in the MTHFR gene, the function of this enzyme changes.

These functional changes caused by mutation also negatively affect the conversion of vitamins, minerals and proteins into an effective form in our body. This mutation, which is thought to have an effect on diseases such as cardiovascular diseases, Parkinson’s disease, Alzheimer’s and cancer, also prevents the excretion of toxins from the body and the absorption of vitamins.

How Is Gene Mutation Detected?

Most people do not know that one of the causes of their chronic diseases is genetics. It is possible to find out whether you have this genetic polymorphism in your genes by gene analysis. You can get more detailed information about your condition with the gene analysis performed on the blood sample taken from the patient.

gene mutation causes

Unfortunately, it is not possible to correct this change in genes. However, aggravating diseases can be prevented by taking some precautions. For example, for the treatment of MTHFR A1298C, even regulating the eating habits in accordance with this mutation will relieve you. If you wish, you can get information from our forum bet, those who live low due to Blood Coagulation.