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The ADGRE2 gene is involved in various health conditions and diseases. One such condition is urticaria, which can be caused by a variant in this gene. Scientific studies have shown repetitive mutations in the ADGRE2 gene, indicating its role in the development and progression of urticaria.

There are numerous references available on this gene, including scientific articles, scientific databases, and the Online Mendelian Inheritance in Man (OMIM) database. These resources provide additional information on the genetic changes associated with ADGRE2 and its impact on related diseases.

In addition to urticaria, the ADGRE2 gene has been linked to other genetic diseases. These include vibratory urticaria and various central and peripheral diseases related to adhesion. Genetic testing can be performed to identify mutations in the ADGRE2 gene and provide a definitive diagnosis for individuals with these conditions.

The ADGRE2 gene is listed in various genetic databases and registries, such as Pubmed and OMIM. These resources provide a comprehensive catalog of genetic changes in the ADGRE2 gene and information on the conditions associated with these changes. Genetic testing can help identify individuals with these genetic variants and guide appropriate treatment plans.

Genetic changes in the ADGRE2 gene have been associated with a number of health conditions. Here are some diseases and conditions related to genetic changes in this gene:

  • Vibratory Urticaria: ADGRE2 gene variant has been found to be associated with vibratory urticaria, a condition characterized by hives and skin rashes triggered by vibrations.
  • Repetitive Repetitive Urticaria: Another variant in the ADGRE2 gene has been linked to repetitive repetitive urticaria, a condition in which patients experience recurrent episodes of hives and rash.
  • Cell-Cell Adhesion: Genetic changes in the ADGRE2 gene may also affect cell-cell adhesion, which is important for the proper functioning of various organs and tissues in the body.

The information on specific genetic changes and their associated health conditions can be found in various databases and scientific articles. Some of the resources for finding information on ADGRE2 gene mutations and related health conditions include:

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  1. OMIM (Online Mendelian Inheritance in Man): This database provides comprehensive information on genes, genetic variants, and their associated health conditions.
  2. The Human Gene Mutation Database (HGMD): A central registry of published gene mutations and related health conditions.
  3. PubMed: A vast collection of scientific articles containing information on genetic changes, diseases, and their relationships.

Additional references, names of specific genetic variants, and tests for detecting these variants can be found in these resources. It is important to consult with healthcare professionals for accurate diagnosis and management of health conditions related to genetic changes in the ADGRE2 gene.

Vibratory urticaria

Vibratory urticaria is a rare condition characterized by the development of hives or rash as a result of exposure to vibration. This condition can cause significant discomfort and can have a negative impact on the individual’s quality of life.

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Research on vibratory urticaria is ongoing, and various studies have been conducted to better understand the underlying causes and mechanisms of this condition. One useful resource for finding scientific information on this topic is PubMed, a database that provides access to a wide range of research articles.

By searching for “vibratory urticaria” on PubMed, researchers can find articles that discuss the symptoms, diagnostic tests, treatment options, and other relevant information related to this condition. This can be helpful in obtaining a comprehensive understanding of vibratory urticaria and its impact on the patient’s health.

In addition to PubMed, there are other resources that provide information on vibratory urticaria. For example, the Online Mendelian Inheritance in Man (OMIM) database contains detailed information on genetic changes and associated diseases. By searching for the ADGRE2 gene, which is related to vibratory urticaria, researchers can find additional information on this condition.

The Genetic Testing Registry is another valuable resource for finding information on vibratory urticaria. This registry lists genetic tests available for various conditions, including vibratory urticaria. The registry provides information on the genes associated with this condition, as well as the tests available for diagnosis and monitoring.

Furthermore, the Central Mutation Databases provide a collection of genetic variants that have been associated with various diseases, including vibratory urticaria. These databases can be useful in identifying specific genetic changes that may be contributing to the development of this condition.

In conclusion, vibratory urticaria is a rare condition that can cause hives or rash as a result of vibration exposure. Research on this condition is ongoing, and PubMed, along with other resources such as the OMIM database and the Genetic Testing Registry, can provide valuable information on diagnostic tests, genetic changes, and other relevant topics related to vibratory urticaria.

Other Names for This Gene

The ADGRE2 gene is also known by the following names:

  • CD312 antigen
  • GPR183L1
  • ELA2
  • Ox2R-LIKE

These names are listed as other names for the ADGRE2 gene in scientific databases such as PubMed and OMIM. They provide additional information and resources for genetic testing, health conditions, and related genes. Variant or mutation in this gene can be associated with diseases, such as urticaria or vibratory angioedema, as referenced in the Genetic Testing Registry. Changes to this gene have been documented in various scientific studies published in PubMed. Centralized databases like OMIM also provide information on this gene and its associated conditions.

Additional Information Resources

  • Names: ADGRE2 gene
  • OMIM: The Online Mendelian Inheritance in Man (OMIM) database provides information on genes, genetic mutation, and related diseases. The ADGRE2 gene may have entries in OMIM.
  • Testing: Testing for changes or variants in the ADGRE2 gene can be done through genetic testing. There are various genetic testing options available to determine any mutations or variations in this gene.
  • Additional Resources: Apart from OMIM, you can find additional information on ADGRE2 gene and related topics in scientific databases, journals, and articles. PubMed is a reputable database that provides information on various scientific publications related to this gene and its functions.
  • Other listed resources: You can also refer to other listed resources like the Genetic Testing Registry which provides information on genetic tests and testing laboratories, and the Genetic Adhesion Database which focuses on genes related to cell adhesion and repetitive vibratory urticaria.
  • References: It is important to consult references and relevant scientific articles to gain a comprehensive understanding of the ADGRE2 gene and its role in diseases or conditions.
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Tests Listed in the Genetic Testing Registry

The Genetic Testing Registry (GTR) is a central registry of genetic tests, providing information on the scientific and clinical validity of genetic testing. It compiles information from various resources, such as PubMed, OMIM, Genetic Association Database (GAD), and other databases.

The GTR lists tests related to the ADGRE2 gene, which is associated with vibratory urticaria, a genetic condition characterized by hives and itching triggered by vibration. The gene variant in ADGRE2 that changes in this condition is called a mutation.

These tests listed in the GTR provide information on the genetic variant in the ADGRE2 gene and its association with vibratory urticaria. They are useful for diagnosing the condition, predicting disease severity, and providing information for genetic counseling.

Some of the tests listed in the GTR are:

  • Test 1: This test detects the specific mutation in the ADGRE2 gene that causes vibratory urticaria.
  • Test 2: This test analyzes the ADGRE2 gene for any genetic variants associated with vibratory urticaria.
  • Test 3: This test provides information on the prevalence of the ADGRE2 gene variant in populations with vibratory urticaria.

These tests can be used by healthcare professionals and researchers to further understand the genetic basis of vibratory urticaria, develop targeted therapies, and improve patient management.

For more information on these tests and other genetic conditions, you can refer to the GTR, PubMed, OMIM, and other related resources.

Scientific Articles on PubMed

PubMed is a database that provides access to a vast collection of scientific articles related to various aspects of health and medicine. It is a valuable resource for researchers and healthcare professionals looking for up-to-date information on different genes and their involvement in diseases and conditions.

The ADGRE2 gene is a repetitive variant gene from which information can be found in PubMed. It is listed in various databases and resources, such as OMIM, which provides detailed information on genetic mutation and related conditions. PubMed Central is another database that contains articles on ADGRE2 gene and its role in different diseases.

Scientific articles related to ADGRE2 gene can be found using PubMed search. When searching for articles on this gene, it is important to use relevant keywords such as “ADGRE2 gene,” “ADGRE2,” or “repetitive variant gene” to narrow down the search results.

In addition to ADGRE2 gene, PubMed also provides information on other genes and their involvement in different diseases. These articles can be found by searching for the gene names or related conditions.

PubMed also provides references and citations for the articles, making it easier to find additional resources and related studies. This information can be helpful for researchers looking to explore further into the topic or for those interested in genetic testing and registry.

Overall, PubMed is a valuable resource for accessing scientific articles on various genes and their role in diseases and conditions. It provides a comprehensive catalog of research findings and can help to further our understanding of genetic changes and their impact on health.

Catalog of Genes and Diseases from OMIM

OMIM (Online Mendelian Inheritance in Man) is a comprehensive catalog of genes and diseases. It provides valuable resources for researchers, scientists, and healthcare professionals to access information on genetic variants and associated diseases.

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OMIM is a database that contains information from scientific articles, including PubMed, on genetic variants and their impact on health. It also includes information on gene names, variant names, and additional references for further reading.

The catalog lists genes and diseases in an organized manner, making it easy to search for specific information. It also provides information on genetic testing for specific conditions, such as central repetitive vibratory urticaria, and changes in genes associated with these conditions.

OMIM is one of the most trusted and comprehensive databases for genetic information. It serves as a registry for genetic diseases, helping healthcare professionals and researchers to access up-to-date and reliable resources.

In conclusion, OMIM is a valuable catalog of genes and diseases that provides essential information on genetic variants and associated diseases. It is a reliable resource that supports scientific research and promotes understanding of genetic conditions.

Gene and Variant Databases

When researching the ADGRE2 gene and its variants, there are several gene and variant databases available. These databases provide valuable information on genetic changes, mutations, and diseases related to this gene.

One of the main databases to consult is the Online Mendelian Inheritance in Man (OMIM) database. This central resource provides comprehensive information on genes and genetic conditions. It lists the ADGRE2 gene and its related diseases, including repetitive urticaria, variant Crouzon syndrome, and other conditions linked to ADGRE2 mutations.

Another valuable resource is PubMed, a database of scientific articles. By searching for the ADGRE2 gene or its variants, researchers can find relevant studies, test results, and genetic changes associated with this gene. PubMed provides references to articles from various scientific journals and publications.

In addition to these databases, there are other genetic resources available online. The Genetic Testing Registry (GTR) offers information on genetic tests conducted for ADGRE2 and its variants. It catalogs the tests available and provides information on their clinical validity and utility.

Furthermore, genetic variant databases, such as the Catalog of Somatic Mutations in Cancer (COSMIC) and the Exome Aggregation Consortium (ExAC), provide data on genetic variations and mutations occurring in the ADGRE2 gene. These databases offer insights into the frequency and distribution of specific genetic changes in the general population and in various diseases.

Overall, the gene and variant databases mentioned above play a crucial role in gathering and disseminating information on the ADGRE2 gene and its variants. Researchers and healthcare professionals can rely on these resources to access information on genetic changes, diseases, and testing options related to ADGRE2.

References

The ADGRE2 gene, also known as F11R or JAM-A, has been studied extensively in scientific research. The following references provide information on the gene, its variants, and related genetic conditions:

  • OMIM (Online Mendelian Inheritance in Man): ADGRE2 gene
  • GeneCards: ADGRE2
  • PubMed: Articles on ADGRE2
  • Genetic Testing Registry: ADGRE2 gene
  • Scientific Catalog: ADGRE2 gene

These databases and resources provide names, information, and testing options for variants of the ADGRE2 gene. They also list related genes and conditions, such as urticaria and vibratory urticaria.

Additional references on genetic mutations and testing for ADGRE2 and related conditions can be found in PubMed articles.

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