Expert

The WWP1 gene, also known as the WWP1 E3 ubiquitin ligase, is a gene that plays a crucial role in various cellular processes. It has been found to be associated with the development of certain cancers, such as Cowden syndrome.…

The LHCGR gene provides instructions for making a protein called luteinizing hormone/choriogonadotropin receptor (LHCGR). This receptor is found on the surface of cells in the testes and ovaries, where it helps coordinate the production and release of sex hormones. The…

The cholinergic system plays a crucial role in the nervous system, and it is involved in various processes such as memory, learning, and attention. Several genes are part of this system, including the cholinergic receptor genes. One of these genes…

The PLCG2 gene, also known as phospholipase C gamma 2, is a key gene involved in immune system regulation and defense against invasive pathogens. It is similar to other genes found in various organisms, indicating its importance in maintaining health…

The KCTD1 gene, also known as the potassium channel tetramerization domain containing 1 gene, is related to various diseases and conditions. It is a scientific term used to describe a specific gene that has been extensively studied and researched. Through…

Fundus albipunctatus is a rare genetic disease characterized by impaired visual function. The condition is typically inherited in an autosomal recessive manner, meaning that both parents must carry a mutated gene in order for their child to have the condition.…

The NSD1 gene, also known as Nuclear Receptor Binding SET Domain Protein 1, is a genetic domain that plays a crucial role in various biological processes. It is located on chromosome 5q35.2 and encodes a protein involved in the regulation…

The NOG gene is a gene that plays a crucial role in the development of bones and joints in the human body. It is a member of the noggin family and is located on chromosome 17. Mutations in this gene…

The GAN gene is a genetic variant that has been associated with various health conditions. It is also known as gigaxonin, a protein involved in the axonal changes that cause gigaxonin, a type of axonal neuropathy. This gene has been…

Costeff syndrome, also known as optic atrophy type 3, is a rare genetic condition that affects the eyes and movement. It was first described in scientific articles in the mid-1990s and has since been cataloged by various organizations and databases,…