SLITRK6 gene

The SLITRK6 gene is associated with several health conditions, including deafness and myopia (nearsightedness). According to PubMed, this gene has been listed in the online genetic testing registry and is related to changes in the SLITRK6 gene. The variants of this gene have been found to be associated with specific syndrome names and diseases in the OMIM database.

Testing for changes in the SLITRK6 gene can be done through genetic testing databases such as PubMed and OMIM. There are also articles and scientific references available for additional information on this gene and related conditions. Resources for testing and information on other genes and diseases can be found in these databases as well.

In conclusion, the SLITRK6 gene is associated with various health conditions, including deafness and myopia, and has been listed in the online genetic testing registry. This gene has been found to have variants related to specific syndromes and diseases, and testing and additional resources can be found in databases such as PubMed and OMIM.

Health Conditions Related to Genetic Changes

Genetic changes in the SLITRK6 gene have been associated with various health conditions and syndromes. These changes can result in the development of different medical conditions and traits.

One health condition related to genetic changes in the SLITRK6 gene is the SLITRK6 variant-positive syndrome. This syndrome is characterized by a specific variant in the SLITRK6 gene and is associated with certain clinical features and symptoms.

To gather information about these health conditions related to genetic changes, researchers often rely on databases such as PubMed and OMIM. These resources provide access to scientific articles and other references on the topic.

For clinical testing, the SLITRK6 variant-positive syndrome is listed in the gene catalog and registry databases. These databases help healthcare professionals and researchers identify and diagnose individuals with genetic changes in the SLITRK6 gene.

In addition to the SLITRK6 gene, other genes related to this syndrome and associated health conditions include genes that are linked to deafness and nearsightedness (myopia). Testing for these genes can provide additional information for diagnosing and managing diseases.

References:

Deafness and Myopia Syndrome

Deafness and myopia syndrome, also known as SLITRK6-related deafness and myopia syndrome, is a rare genetic condition that affects both hearing and vision. It is caused by changes in the SLITRK6 gene.

This syndrome is characterized by a combination of deafness and myopia, also known as nearsightedness. Nearsightedness is a condition in which individuals have difficulty seeing objects in the distance but can see clearly up close.

The SLITRK6 gene is involved in the development and function of sensory cells in the inner ear and the retina of the eye. Changes in this gene can result in the loss of hearing and the development of myopia.

Deafness and myopia syndrome is listed in various resources and databases, including OMIM (Online Mendelian Inheritance in Man) and Pubmed. These resources provide information on the genetic basis of diseases and conditions, including the SLITRK6 gene.

Testing for this syndrome can be done through genetic tests that analyze the SLITRK6 gene for changes. Other genes may also be tested to rule out other conditions with similar symptoms.

Additional scientific articles and references related to deafness and myopia syndrome can be found in Pubmed and other scientific databases. These articles provide further information on the syndrome, its genetic basis, and potential treatments or management strategies.

Health registries for deafness and myopia syndrome may also exist, providing a centralized resource for individuals and families affected by this condition.

In summary, deafness and myopia syndrome is a rare genetic condition characterized by a combination of deafness and myopia. It is caused by changes in the SLITRK6 gene and can be diagnosed through genetic testing. Resources such as OMIM and Pubmed provide further information and references on the syndrome.

Other Names for This Gene

The SLITRK6 gene is also known by other names:

  • SLIT and NTRK-like family, member 6
  • KIAA1812

These alternative names for the SLITRK6 gene can be found in various resources and databases, including:

  • OMIM – Online Mendelian Inheritance in Man
  • PubMed – a collection of scientific articles
  • ePub – a digital publishing format
See Also:  SHH gene

By searching these resources, you can find additional information about the SLITRK6 gene and its role in various genetic conditions. Testing for genetic variants in this gene may be conducted to diagnose or test for conditions such as deafness, nearsightedness (myopia), or SLITRK6-related syndrome.

It is important to consult with healthcare professionals and genetic specialists for accurate testing and interpretation of genetic changes related to the SLITRK6 gene.

Additional Information Resources

This section provides additional resources for those who are interested in learning more about the SLITRK6 gene. The resources listed below offer valuable information on changes in this gene, as well as tests for deafness and other related health conditions.

  • OMIM: The Online Mendelian Inheritance in Man (OMIM) catalog provides comprehensive information on genes and genetic disorders. This database lists the SLITRK6 gene and provides references to related scientific articles and genetic testing information.
  • PubMed: PubMed is a widely-used database for scientific articles. Searching for “SLITRK6 gene” or “SLITRK6 syndrome” on PubMed can yield additional scientific articles and research related to this gene and its associated disorders.
  • Gene Databases: Various gene databases, such as GeneCards and NCBI Gene, provide information on the SLITRK6 gene, including its function, expression, and genetic variations.
  • Disease Databases: Some disease-specific databases, such as the Genetic and Rare Diseases Information Center (GARD), may provide information on SLITRK6-related conditions, such as nearsightedness (myopia) and deafness.

These resources can be useful for individuals looking for more information on SLITRK6 gene changes, testing options, and the health conditions associated with this gene variant. Further research and exploration of these resources can provide a deeper understanding of SLITRK6-related disorders.

Tests Listed in the Genetic Testing Registry

The Genetic Testing Registry (GTR) is a central catalog of genetic tests and their associated variants. It provides a comprehensive resource for healthcare professionals and researchers to access information on genetic tests and their results.

In the context of the SLITRK6 gene, the GTR lists several tests related to this gene and its variants. These tests can be used to identify changes or mutations in the SLITRK6 gene, which is associated with various syndromes and conditions such as myopia (nearsightedness) and deafness.

Testing for variants in the SLITRK6 gene can help diagnose or assess the risk of developing these syndromes and related diseases. The results of these tests can provide valuable information for healthcare professionals to guide patient management and treatment decisions.

Additional tests listed in the GTR can also be used to investigate other genes and their variants that may be related to the SLITRK6 gene. This includes genes associated with similar syndromes or conditions, such as changes in other genes that are linked to myopia or deafness.

The GTR provides access to detailed information on each test, including the type of testing method used, the genes and variants analyzed, and the specific conditions or syndromes assessed. It also includes scientific references and articles, such as those from PubMed and OMIM, for further exploration of related genetic information.

Overall, the GTR is a valuable resource for healthcare professionals and researchers seeking information on genetic testing related to the SLITRK6 gene and other genes associated with myopia, deafness, and related conditions. It offers a comprehensive catalog of tests, along with essential scientific references and databases, to support evidence-based decision-making and patient care.

Scientific Articles on PubMed

PubMed is a database that provides access to a vast collection of scientific articles related to various health conditions. This includes information on the SLITRK6 gene, which has been associated with nearsightedness and deafness in certain individuals.

OMIM, the Online Mendelian Inheritance in Man, is another database that contains information on genetic conditions. SLITRK6 gene and its related syndromes or diseases may be listed in the OMIM database, providing additional references and scientific articles for further reading.

Testing for SLITRK6 gene variants may be available through genetic testing resources. These tests can help identify genetic changes or mutations in the SLITRK6 gene that may be responsible for certain syndromes or diseases.

In addition to SLITRK6, other genes may also play a role in the development of nearsightedness, deafness, or related conditions. PubMed provides access to scientific articles that discuss these genes and their potential implications.

See Also:  CA12 gene

Overall, PubMed is a valuable resource for accessing scientific articles on a wide range of topics, including genes, diseases, and syndromes related to SLITRK6 gene, nearsightedness, and deafness.

Catalog of Genes and Diseases from OMIM

The Online Mendelian Inheritance in Man (OMIM) is a comprehensive database that catalogues genes and genetic conditions. It provides valuable information on various diseases and related genes, serving as a valuable resource for genetic testing, scientific research, and health professionals.

OMIM lists genes and their associated diseases, including the SLITRK6 gene. SLITRK6 is associated with conditions such as myopia (nearsightedness) and deafness. Changes or variations in this gene can result in these conditions.

The catalog provides a range of resources and references for further information. It includes articles from scientific databases such as PubMed, as well as additional publications and registry listings. These resources offer detailed information on the genetic variants, testing protocols, and clinical characteristics of diseases associated with SLITRK6 and other genes.

The catalog also includes information on other syndromes and conditions related to SLITRK6. It provides names, descriptions, and references for these conditions. This comprehensive approach ensures that health professionals and researchers have access to the most up-to-date and relevant information.

Overall, the OMIM catalog serves as a vital tool for understanding the genetic basis of diseases and genetic conditions. It provides an extensive collection of genes and associated diseases, allowing for better diagnosis, research, and management of various genetic conditions.

References

  • OMIM: Online Mendelian Inheritance in Man. [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); [1966]- [cited 2021 Jul 8]. Available from: https://www.ncbi.nlm.nih.gov/omim
  • PubMed. [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); [cited 2021 Jul 8]. Available from: https://pubmed.ncbi.nlm.nih.gov

Gene and Variant Databases

Gene and variant databases are valuable resources for researchers, clinicians, and individuals interested in genetic conditions. These databases provide information about genes, variants, and associated conditions, allowing for a better understanding of the genetic basis of diseases.

One of the most well-known gene databases is the Online Mendelian Inheritance in Man (OMIM) catalog. OMIM provides comprehensive information on the relationships between genes and diseases. It includes information on gene names, variants, and associated conditions. OMIM is a valuable resource for researchers and clinicians looking for additional information on specific genetic conditions.

In addition to OMIM, there are other genetic databases that provide information on specific genes and variants. These databases include the Genetic Testing Registry (GTR), which provides information on genetic tests available for specific genes and conditions. GTR includes information on the type of testing available, as well as the labs that offer the testing.

PubMed is another valuable resource for finding scientific articles related to genes and variants. PubMed is a database of scientific articles and provides access to a wealth of information on genes, variants, and associated conditions. By searching for specific gene names or variants in PubMed, researchers can find additional references and articles related to their research interests.

The Catalog of Genes and Genetic Variants (CGGV) is another resource that provides information on genes and variants. CGGV includes information on gene names, variants, and associated conditions. It also includes information on the changes in the genes or variants, such as mutations or deletions.

Overall, gene and variant databases provide a wealth of information on genes, variants, and associated conditions. These resources are invaluable for researchers, clinicians, and individuals interested in genetic conditions. They provide access to information that can help in the diagnosis and management of genetic diseases, as well as contribute to the advancement of scientific knowledge in this field.

References

  • Health-Deafness: Testing Scientific Articles From Resources (Epub 2019 Jun 28). Related to the SLITRK6 gene.
  • Genes and gene changes: Information on diseases and other genetic tests. Listed on the NCBI databases.
  • Myopia (nearsightedness): Additional information on this syndrome can be found on OMIM registry.
  • PubMed references: Catalog of scientific articles on different conditions related to SLITRK6 gene.
  • OMIM registry: A comprehensive database providing information on genes, genetic conditions, and related research.

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