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The F7 gene is a genetic factor that is responsible for the production of coagulation factor VII (FVII) in the bloodstream. FVII is a protein involved in the blood clotting process. Mutations in the F7 gene can lead to a deficiency or dysfunction of FVII, resulting in a condition known as factor VII deficiency.

Factor VII deficiency is a rare genetic disorder that can cause excessive bleeding, particularly from the nose, gums, and gastrointestinal tract. This condition can be inherited in an autosomal recessive or autosomal dominant manner. Individuals with this disorder may have a variety of symptoms ranging from mild to severe.

The F7 gene is listed in various genetic databases and resources, including OMIM and PubMed. These resources provide additional information on the gene, its variants, and the associated conditions. In addition, there are clinical registries and testing laboratories that offer diagnostic testing and resources for individuals with suspected factor VII deficiency.

Research and scientific articles on the F7 gene and related conditions are available, providing valuable information for healthcare professionals and individuals interested in learning more about this genetic factor. Genetic testing can help confirm a diagnosis and identify specific changes or variants in the F7 gene that may be contributing to the condition.

Genetic changes or variants in the F7 (coagulation factor VII) gene can lead to various health conditions and disorders. These genetic changes can result in a deficiency or abnormality in the production or function of coagulation factor VII, which is essential for blood clotting.

The following resources and databases provide valuable information on the health conditions related to genetic changes in the F7 gene:

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  • OMIM: OMIM (Online Mendelian Inheritance in Man) is a comprehensive catalog of human genes and genetic disorders. It provides detailed information on the various genetic changes or variants associated with coagulation factor VII deficiency or abnormality.
  • Genetic Testing Registry: The Genetic Testing Registry (GTR) is a central repository for information about genetic tests. It lists the available genetic tests for the F7 gene and related health conditions.
  • PubMed: PubMed is a vast database of scientific articles on various topics, including genetic conditions. Searching for relevant keywords, such as “F7 gene” or “coagulation factor VII deficiency,” in PubMed can provide access to the latest research and clinical studies on health conditions related to genetic changes in the F7 gene.

Clinical registries and blood disorder registries can also provide valuable information on the prevalence, clinical presentation, and management of health conditions related to genetic changes in the F7 gene. Additional factors such as environmental and lifestyle factors may also contribute to the development and severity of these conditions.

Consulting with healthcare professionals and genetic specialists is essential for accurate diagnosis, genetic testing, and appropriate management of health conditions associated with genetic changes in the F7 gene. They can provide comprehensive evaluations, genetic counseling, and personalized treatment plans based on individual cases and genetic profiles.

Factor VII deficiency

Factor VII deficiency is a genetic disorder that affects the blood’s ability to clot properly. It is caused by a deficiency in the F7 gene, which provides instructions for making a protein called factor VII. This protein plays a crucial role in the clotting cascade, which helps stop bleeding in the bloodstream.

This condition is listed in the OMIM genetic disorder catalog and can be found in other scientific databases, such as PubMed. References to articles and additional clinical information related to Factor VII deficiency can be accessed through these resources.

See also  WNK1 gene

Testing for Factor VII deficiency involves analyzing the F7 gene for changes or deletions that may be associated with the condition. Diagnostic tests may also include measuring the levels of factor VII in the blood.

The Factor VII Registry is a valuable resource for individuals and families affected by this condition. It provides a platform for sharing and gathering information on the genetic variants, health conditions, and clinical features associated with Factor VII deficiency.

Other genes and factors involved in the clotting cascade may also be listed in the registry. It is important to consider these interconnected factors, as their interactions contribute to the overall clotting process and can impact the severity and clinical outcomes of Factor VII deficiency.

In summary, Factor VII deficiency is a genetic condition that affects the blood’s ability to clot properly. The F7 gene plays a crucial role in this process, and changes or deletions in this gene can lead to the development of the disorder. Resources such as OMIM and the Factor VII Registry provide valuable information and support for individuals affected by this condition.

Other Names for This Gene

  • F7
  • Coagulation Factor VII
  • Proconvertin
  • Serum Prothrombin Conversion Accelerator
  • Serine protease 3G4
  • Activating factor III
  • Prothrombinase

The F7 gene, also known as Coagulation Factor VII, has several other names by which it is referred to in various scientific articles, databases, and resources related to genetic conditions and health. These alternative names are used to facilitate easy identification of the gene and its associated factors in testing, clinical studies, and research.

The genetic changes in the F7 gene can lead to deficiencies or variants in the coagulation factor VII, which in turn can result in disorders related to blood clotting. To compile information on these conditions, the gene and its related factors are cataloged in databases such as OMIM (Online Mendelian Inheritance in Man), PubMed, and the Clinical Genomic Database.

References to the F7 gene and its various names can be found in scientific articles, research papers, and clinical studies. The names listed above are commonly used to refer to this gene and its associated factors in these resources.

Additional information on the F7 gene and its related conditions can be found in the Genetic and Rare Diseases Information Center, the Online Mendelian Inheritance in Man, and the Clinical Genomic Database. These resources provide valuable insights into the genetic factors and clinical implications of F7 gene deficiencies or variants.

Overall, the F7 gene, also known by its alternative names, plays a critical role in blood clotting and its deficiency or variant can have significant health implications. The mentioned alternative names are used to ensure effective communication and understanding of the gene and its associated factors in scientific and clinical contexts.

Additional Information Resources

For additional information on the F7 gene and related conditions, the following resources may be useful:

  • The Genetic Testing Registry (GTR): Provides information about genetic tests for this condition. The GTR is a central repository for genetic test information and includes testing laboratories and related information.
  • The Genetic and Rare Diseases Information Center (GARD): Offers information on the F7 gene and related disorders. GARD provides resources for patients and their families, including a genetic disease catalog and contact information for patient support groups.
  • The Online Mendelian Inheritance in Man (OMIM): A comprehensive database that provides information on genetic conditions and the genes associated with them. OMIM contains scientific and clinical information, including references to articles and other resources.
  • PubMed: A database of scientific articles from biomedical literature. PubMed can be used to find research papers and studies on the F7 gene and its associated conditions.

These resources can provide up-to-date information on the genetic changes, symptoms, testing, and treatment options for F7 gene-related conditions. They can also help connect individuals and families affected by these disorders to support groups and health care providers with expertise in these conditions.

Tests Listed in the Genetic Testing Registry

The Genetic Testing Registry is a catalog of genetic tests and the associated clinical conditions for which they are used. It provides information about genes, variants, and other factors related to genetic testing.

See also  EIF2B4 gene

This registry contains a wealth of scientific and clinical resources, including articles from PubMed and OMIM, as well as references to other databases. It is a valuable tool for healthcare professionals and researchers seeking information on specific genetic disorders and conditions.

One of the genetic tests listed in this registry is for the F7 gene, which is associated with Factor VII deficiency. Factor VII deficiency is a rare blood disorder that can lead to bleeding and other health problems.

The testing listed in the registry includes both genetic testing and blood testing. Genetic testing examines changes in the F7 gene that may be associated with Factor VII deficiency. Blood testing evaluates the level of Factor VII in the bloodstream.

For additional information about the testing listed in the registry, including testing methods and resources, it is recommended to consult the specific test entry in the Genetic Testing Registry.

Overall, the Genetic Testing Registry serves as a valuable resource for healthcare professionals, researchers, and individuals seeking information on genetic tests and associated clinical conditions. It provides a comprehensive catalog of genes, variants, and other factors related to genetic testing, making it an essential tool in the field of genetic medicine.

Scientific Articles on PubMed

Scientific articles on PubMed provide valuable information about the F7 gene and its related clinical factors. Here is a list of resources that can be found on PubMed:

  • Genes and Genetic Testing: Articles that discuss the F7 gene and its variations, as well as the testing methods used to detect F7 gene deficiency.
  • Health Conditions and Diseases: Articles that investigate the role of the F7 gene in various health conditions and diseases.
  • Registry and Catalog Databases: References to registry and catalog databases where additional information about the F7 gene and related disorders can be found.
  • Blood and Bloodstream: Articles that explore the relationship between the F7 gene and blood-related factors, such as clotting disorders.
  • Clinical Factors: Articles that discuss the clinical factors associated with F7 gene deficiency, including symptoms, diagnosis, and treatment options.
  • Scientific Articles: Peer-reviewed scientific articles that present research findings related to the F7 gene and its impact on health.
  • OMIM: References to articles available on the Online Mendelian Inheritance in Man (OMIM) database, which provides in-depth information about genetic conditions and their associated genes.
  • Additional Resources: Articles that mention additional resources and databases for further information on the F7 gene and related conditions.

PubMed is a valuable research tool for gathering scientific knowledge on genetic factors like the F7 gene. By exploring the articles available in the database, researchers and healthcare professionals can gain a better understanding of the F7 gene’s role in various health conditions and diseases.

Catalog of Genes and Diseases from OMIM

OMIM (Online Mendelian Inheritance in Man) is a registry of genetic conditions, genes, and variants associated with human diseases. It provides a comprehensive catalog of genes and diseases based on scientific research and clinical information.

The OMIM database is a valuable resource for researchers, healthcare professionals, and individuals interested in genetic health. It lists information on genetic conditions and genes from various references, including scientific articles, clinical databases, and other genetic resources.

One of the genes listed in the OMIM database is the F7 gene, which encodes for coagulation factor VII (VII). Mutations in this gene can lead to factor VII deficiency, a condition characterized by abnormal bleeding and clotting problems.

OMIM provides information on the F7 gene, including genetic tests available for testing F7 variants and associated diseases. It also includes a list of related conditions and changes in the F7 gene that have been reported in the scientific literature.

Researchers and healthcare professionals can use the OMIM database to access information on specific genes, diseases, and related clinical conditions. This can aid in the diagnosis, management, and treatment of genetic disorders.

See also  ITM2B gene

In addition to F7 and factor VII deficiency, the OMIM database covers a wide range of genes and diseases. The registry includes information on blood-related conditions, such as hemophilia and other clotting disorders, as well as other genetic diseases affecting various organ systems and functions.

OMIM references the sources of information for each gene and disease entry, including relevant articles from PubMed and other scientific databases. This ensures that the information provided in the database is based on reliable and up-to-date scientific research.

In conclusion, the Catalog of Genes and Diseases from OMIM is a valuable resource for accessing information on genetic conditions, genes, and related clinical conditions. It serves as a comprehensive registry of genetic diseases, providing information on specific genes, variants, and associated clinical features. Healthcare professionals, researchers, and individuals interested in genetic health can benefit from the wealth of information available on OMIM.

Gene and Variant Databases

A gene and variant database is a collection of information related to genes and their associated variants. These databases provide vital resources for researchers, clinicians, and individuals interested in genetic conditions. They contain data on gene names, variant names, the factors contributing to the genetic condition, and testing options.

Genetic testing is an important tool for diagnosing genetic disorders. The information stored in these databases can help facilitate the testing process by providing a catalog of known gene variants and their associated diseases. Clinicians can use this information to select appropriate tests and interpret the results.

One widely used gene and variant database is the Online Mendelian Inheritance in Man (OMIM). OMIM is a comprehensive resource that provides detailed information on genetic disorders and their associated genes. It includes scientific articles, clinical descriptions, and references to other resources.

Another important database is the Human Gene Mutation Database (HGMD), which focuses specifically on disease-causing mutations. HGMD provides information on genetic changes that have been reported in the scientific literature and have been confirmed to be disease-causing.

For gene-specific databases, the F7 gene, which encodes the coagulation factor VII (FVII) protein, has its own variant database. The F7 Variant Database is a registry of genetic variants in the F7 gene and their association with FVII deficiency, a rare bleeding disorder. It provides information on the clinical significance of specific variants and their impact on FVII function.

These gene and variant databases play a crucial role in advancing our understanding of genetic conditions and improving patient care. They serve as valuable resources for researchers studying the genetic basis of diseases and for clinicians making diagnoses based on genetic testing.

Overall, gene and variant databases provide a wealth of information on genes, variants, and their relationship to diseases. They are an essential tool for genetic research, clinical decision-making, and patient care.

  • Gene and variant databases are collections of information related to genes and their associated variants.
  • They provide gene names, variant names, and factors contributing to genetic conditions.
  • These databases facilitate genetic testing by providing a catalog of known gene variants and associated diseases.
  • Notable databases include Online Mendelian Inheritance in Man (OMIM) and Human Gene Mutation Database (HGMD).
  • Gene-specific databases, like the F7 Variant Database, focus on specific genes and associated diseases, such as FVII deficiency.
  • These databases help advance genetic research, improve diagnostic accuracy, and enhance patient care.

References

  • Factor VII Deficiency – Genetics Home Reference – NIH. Available at: https://ghr.nlm.nih.gov/condition/factor-vii-deficiency#resources
  • Catalog of Genes and Diseases from OMIM (1 link). Available at: https://www.omim.org/.
  • Factor VII deficiency – Genetics Home Reference – NIH. Available at: https://ghr.nlm.nih.gov/condition/factor-vii-deficiency#resources
  • Factor VII deficiency – PubMed – NCBI. Available at: https://pubmed.ncbi.nlm.nih.gov/?term=factor+vii+deficiency.
  • Factor VII deficiency – Genetics Home Reference – NIH. Available at: https://ghr.nlm.nih.gov/condition/factor-vii-deficiency#resources
  • OMIM. Available at: https://www.omim.org/.
  • Factor VII deficiency – Genetics Home Reference – NIH. Available at: https://ghr.nlm.nih.gov/condition/factor-vii-deficiency#resources
  • Factor VII deficiency – Genetic and Rare Diseases Information Center – NIH. Available at: https://rarediseases.info.nih.gov/diseases/10152/factor-vii-deficiency.
  • Factor VII deficiency – Genetics Home Reference – NIH. Available at: https://ghr.nlm.nih.gov/condition/factor-vii-deficiency#resources
  • Factor VII deficiency – Genetic Testing Registry – NIH. Available at: https://www.ncbi.nlm.nih.gov/gtr/tests/29155/factor-vii-deficiency/.

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