The KRT6C gene is a genetic variant that has been identified as being related to several conditions, including palmoplantar keratoderma and pachyonychia congenita. These conditions affect the skin, nails, and other tissues, causing them to become thickened and damaged. The…
Hypermanganesemia with dystonia is a rare genetic condition that causes problems with movement and muscle contractions. It is associated with an excess of manganese in the body. Hypermanganesemia with dystonia is caused by mutations in the SLC39A14 gene, which builds…
The LAMC2 gene is responsible for encoding the gamma-2 subunit of laminin-5, a protein that is important for the health of various tissues in the body. Laminin-5 is a component of the extracellular matrix, which provides structural support and plays…
Hair color is a unique and diverse trait in humans, displaying a wide range of shades and tones. Many people wonder if hair color is determined by genetics, and scientific research has provided some insight into this question. Genetic Factors…
The KRT4 gene, also known as Keratin 4, is a gene that plays a crucial role in the health of the human body. It is a scientific gene that has been extensively studied and researched by professionals in the field.…
Precision medicine is a medical approach that takes into account individual variability in genes, environment, and lifestyle when developing tailored treatment plans. It aims to provide more accurate diagnoses, deliver personalized treatment options, and improve patient outcomes. Precision medicine utilizes…
The CDC6 gene is a genetic variant that encodes a protein involved in the regulation of cell division. This gene is also known as the Meier-Gorlin syndrome gene, as mutations in CDC6 have been linked to this condition. The Meier-Gorlin…
The RYR2 gene, also known as the Ryanodine receptor 2 gene, is a gene that encodes for the ryanodine receptor 2 protein. Mutations in this gene can lead to various diseases and conditions, including arrhythmogenic right ventricular cardiomyopathy, catecholaminergic polymorphic…
The TRPV4 gene is associated with various diseases and disorders characterized by a wide range of symptoms. This gene is listed in databases such as Auer-Grumbach and PubMed, along with other genes and disorders. References and resources on TRPV4-associated diseases…
Genetic conditions are disorders caused by abnormalities in an individual’s genetic material. These conditions can be inherited from one or both parents or arise spontaneously due to mutations in genes. One such genetic condition is Genetic Conditions B. Genetic Conditions…