Contents
[hide]
[show]

The TWIST1 gene, also known as twist-related protein 1, is a catalog of genetic and functional information related to various diseases. This gene has been found to be associated with several genetic disorders and syndromes, including Saethre-Chotzen syndrome. In addition, the TWIST1 gene is listed in databases and variant registries as a factor in the development of certain conditions.

Studies have shown that changes in the TWIST1 gene can lead to abnormal development of tissues and organs. This can result in a range of health problems and medical conditions. Testing for variants in the TWIST1 gene can provide additional information for diagnosis and management of these conditions.

Scientific articles and references on the TWIST1 gene and related conditions can be found in resources such as PubMed and OMIM. These sources provide information on the role of this gene in normal development and the changes that can occur in various diseases. Testing for TWIST1 gene variants is available in some genetic testing laboratories, and it may be recommended for individuals with specific symptoms or a family history of related conditions.

In conclusion, the TWIST1 gene plays a significant role in the development of various genetic disorders and syndromes. Understanding the function of this gene and the conditions associated with it can provide valuable insight into the diagnosis, management, and treatment of these diseases.

Genetic changes can have significant effects on an individual’s health, leading to the development of various conditions and syndromes. The study of these genetic changes and their associated health conditions is crucial for understanding the underlying mechanisms and developing appropriate treatments. Here, we explore some of the health conditions related to genetic changes, with a particular focus on the role of the TWIST1 gene.

TWIST1 gene

Long wait times are often cited as a downfall of universal healthcare systems, but wait times in America have reached a new high, too. The average time to make a physician appointment as a new patient in 15 major U.S. cities is now 24 days, up 30% in just 3 years (2014 to 2018) according to physician recruiting firm Merritt Hawkins.

The TWIST1 gene, located on chromosome 7p21.1, is essential for embryonic development and plays a critical role in regulating cell migration, proliferation, and differentiation. Mutations in this gene have been associated with several health conditions and syndromes, including:

  • Saethre-Chotzen syndrome: Saethre-Chotzen syndrome is a genetic disorder characterized by craniosynostosis, where the bones in the skull fuse prematurely. Mutations in the TWIST1 gene are responsible for a significant proportion of Saethre-Chotzen syndrome cases.
  • Drosophila tangle syndrome: Drosophila tangle syndrome is a neurodegenerative disorder found in fruit flies. Studies in Drosophila have shown that the TWIST1 gene is necessary for the normal development of neural tissues.

Testing for genetic changes

Identifying genetic changes associated with health conditions often involves genetic testing. Several resources, such as PubMed, OMIM, and scientific databases, provide information on genetic changes, genes, and associated health conditions. These resources also list additional names and variants of genes, making it easier to search for specific conditions and genes of interest.

Functional tests, including protein assays and animal models, are often used to study the impact of genetic changes on health. These tests help researchers understand the biological functions of genes and their role in the development of particular conditions. Additionally, genetic testing can be performed on individuals to diagnose and assess their risk for certain diseases.

Health conditions and related genes

Genetic changes can contribute to the development of numerous health conditions beyond those associated with the TWIST1 gene. Many syndromes and diseases are linked to specific genetic alterations, including copy number variations, single nucleotide variants, or structural rearrangements. Conditions related to genetic changes can affect various tissues and organs, leading to a wide range of symptoms and complications.

To gain a comprehensive understanding of health conditions related to genetic changes, it is essential to consult scientific articles, review databases, and reference resources such as PubMed and OMIM. These sources provide up-to-date information on the latest research findings, diagnostic testing methods, and potential treatments for genetic conditions.

In conclusion, genetic changes play a significant role in the development of health conditions. The TWIST1 gene is just one example of how genetic alterations can lead to syndromes and diseases. By studying the functional effects of genetic changes and utilizing testing methods, researchers and healthcare professionals can better understand and address the impact of genetic variations on an individual’s health.

Saethre-Chotzen syndrome

Saethre-Chotzen syndrome is a genetic condition associated with mutations in the TWIST1 gene. It is also known as acrocephalosyndactyly type III and is listed in the OMIM catalog of genetic diseases, under the OMIM number 101400. This condition is named after two scientists, Ingeborg Saethre and A. Chotzen, who first described it in the scientific literature in 1931 and 1932, respectively.

See also  MT-TH gene

Individuals with Saethre-Chotzen syndrome typically have abnormal head shape, fused fingers or toes, and other craniofacial abnormalities. Some individuals may also have intellectual disabilities or hearing loss. These symptoms are caused by changes in the function of the TWIST1 gene, which is involved in the development of tissues and organs in the body.

There are several resources available for testing and information on Saethre-Chotzen syndrome. Genetic testing can be done to identify mutations in the TWIST1 gene and confirm the diagnosis. The Genetic Testing Registry, located on the National Center for Biotechnology Information (NCBI) website, provides information about the available genetic tests for this condition.

Additional information on Saethre-Chotzen syndrome can be found in scientific articles published in PubMed, a database of biomedical literature. PubMed can be searched using keywords such as “Saethre-Chotzen syndrome” or “TWIST1 gene” to find relevant articles.

Other databases, such as OMIM and the Human Gene Mutation Database (HGMD), also provide information on the genetic changes and associated clinical features of Saethre-Chotzen syndrome. These databases can be used to find references and additional scientific resources on this condition.

In summary, Saethre-Chotzen syndrome is a genetic condition caused by mutations in the TWIST1 gene. It is characterized by craniofacial abnormalities, fused fingers or toes, and other symptoms. Genetic testing and information can be obtained from various resources, including the Genetic Testing Registry, PubMed, OMIM, and HGMD.

Other disorders

The TWIST1 gene is also associated with several other disorders. Mutations in this gene can affect the function of other proteins, leading to different conditions. Some of the other disorders related to the TWIST1 gene include:

  • Saethre-Chotzen syndrome: This condition is caused by mutations in the TWIST1 gene and is characterized by abnormalities of the skull and face.
  • Other genetic conditions: Mutations in the TWIST1 gene have been found in individuals with other genetic conditions, although their specific role in these conditions is not fully understood.

In order to diagnose these disorders, several tests may need to be conducted. These tests can include genetic testing to identify changes in the TWIST1 gene, as well as other tests to evaluate the condition of different tissues.

For more information on these disorders, the Online Mendelian Inheritance in Man (OMIM) database and PubMed can be valuable resources. These databases catalog scientific articles and provide additional information on the genetic changes associated with these conditions.

In addition, the National Institutes of Health (NIH) provides information on genetic testing and related resources for these disorders. The NIH offers a registry of genetic tests, which lists the genes and conditions that can be tested for, including the TWIST1 gene.

It is important to note that changes in the TWIST1 gene are not always associated with these disorders. These changes can occur in normal individuals and may not have any significant impact on their health.

For more information on the specific genetic changes associated with these disorders, references to scientific articles, or resources for testing and diagnosis, it is recommended to consult with a healthcare professional or genetic counselor.

Other Names for This Gene

The TWIST1 gene is also known by other names, including:

  • ACRDY6: This name refers to the gene as associated with the autosomal dominant craniosynostosis type 6.
  • BPES2: The gene is also called BPES2 due to its involvement in blepharophimosis, ptosis, and epicanthus inversus syndrome type 2.
  • BPS: Another name attributed to the gene is BPS, which stands for Blepharophimosis, Ptosis, and Strabismus.
  • SMS: SMS is an acronym for Saethre-Chotzen syndrome, a condition associated with mutations in the TWIST1 gene.
  • CS: In addition to Saethre-Chotzen syndrome, the gene is also related to craniosynostosis, another genetic condition.
  • ACRD1: This abbreviation represents autosomal dominant craniosynostosis type 1.

These are just a few of the names used to refer to the TWIST1 gene in different scientific articles, databases, and resources.

Additional Information Resources

If you would like more information about the TWIST1 gene, here are some helpful resources:

  • Online Databases: You can find detailed information about genes, genetic disorders, and other related information on databases such as Genetic Testing Registry (GTR) and Online Mendelian Inheritance in Man (OMIM).
  • Scientific Articles and References: PubMed is a valuable resource to search for scientific articles related to the TWIST1 gene. You can find articles that discuss the functional aspects of this gene, changes and variants in the gene, and its role in various diseases and conditions.
  • Genetic Testing: If you suspect a genetic condition or want to know more about the TWIST1 gene and its association with a particular condition, you may consider genetic testing. There are several tests available that can analyze the twist1 gene and provide information about specific variants and their implications.
  • Related Syndromes: TWIST1 gene is associated with various syndromes and conditions, including Saethre-Chotzen syndrome. Information about these conditions can be found in medical databases, such as OMIM, as well as from patient registries and support groups.
See also  Lateral meningocele syndrome

Please note that this is just a copy of some additional resources available. There may be other resources and information available from different scientific and health organizations. It is always recommended to consult with healthcare professionals or genetic counselors for accurate and up-to-date information.

Tests Listed in the Genetic Testing Registry

The Genetic Testing Registry (GTR) is a centralized database managed by the National Center for Biotechnology Information (NCBI) that provides information about genetic tests. This database contains information about tests, including the TWIST1 gene.

For the TWIST1 gene, the GTR lists the following tests:

  • TWIST1 gene copy number analysis: This test analyzes the copy number of the TWIST1 gene, which is important for its proper functioning.
  • OMIM: TWIST-related disorders test catalog: This catalog provides a comprehensive list of disorders associated with mutations in the TWIST1 gene. It includes disorders such as Saethre-Chotzen syndrome.
  • Listed individual tests: These tests specifically focus on genetic changes in the TWIST1 gene and provide information about the associated conditions.
  • Additional genetic tests: Other genetic tests that may have related genes or proteins, which can provide additional information for diagnosing diseases.

It is important to note that changes in the TWIST1 gene can be associated with various diseases and conditions. These diseases and conditions are referenced in scientific articles available on PubMed and may also be documented in other genetic databases.

Furthermore, the TWIST1 gene plays a crucial role in the development of various tissues and is particularly important for craniosynostosis, a condition characterized by the premature fusion of the skull bones. Mutations in the TWIST1 gene have been linked to Saethre-Chotzen syndrome, a genetic disorder that affects craniofacial development and other aspects of growth and development.

Genetic testing for the TWIST1 gene can help determine if a specific variant or mutation is present. This information can be useful in diagnosing a particular condition or assessing the risk of developing certain diseases.

In summary, the GTR provides information on various tests related to the TWIST1 gene, including tests for copy number analysis, catalog of related disorders, individual tests for genetic changes, and additional tests for related genes and proteins. This information can be crucial in understanding the genetic basis of diseases and conditions associated with the TWIST1 gene.

Scientific Articles on PubMed

The TWIST1 gene is known to produce proteins that are related to the normal genetic and functional processes in the body. Mutations in this gene are associated with a condition called Saethre-Chotzen syndrome. Several variants of the TWIST1 gene have been identified and listed in the OMIM database.

Scientific articles on PubMed provide valuable resources on health and genetic disorders. These articles can be used as references for further research and testing. PubMed is a registry of scientific articles from various sources, including journals and research databases.

Some of the scientific articles on PubMed provide information on changes in the TWIST1 gene region and their association with diseases and conditions. These articles also provide additional information on the genetic tests and diagnostic criteria for Saethre-Chotzen syndrome and other related disorders.

In Drosophila, the twist gene is known to be involved in the development of various tissues and plays a crucial role in embryogenesis. The twist1 gene in humans is homologous to the twist gene in Drosophila, suggesting a similar function in human development.

Some of the scientific articles on PubMed list the names and functions of other genes that are related to TWIST1 and implicated in various diseases and conditions. These articles provide insights into the molecular mechanisms and pathways associated with TWIST1 and its related genes.

Scientific articles on PubMed also provide information on genetic testing and diagnostic resources for TWIST1 and other related genes. This includes information on laboratories and testing facilities that offer genetic tests for TWIST1 mutations and related disorders.

Overall, scientific articles on PubMed are a valuable resource for researchers and healthcare professionals looking to gain a better understanding of the TWIST1 gene and its role in health and disease.

Catalog of Genes and Diseases from OMIM

The OMIM (Online Mendelian Inheritance in Man) database provides a comprehensive catalog of genes and genetic disorders. It includes information on various genes, their associated diseases, and relevant resources for further studies.

The TWIST1 gene is one of the genes listed in the OMIM database. It is involved in various conditions and diseases, and its role in human health has been extensively studied.

Several genetic disorders have been associated with changes in the TWIST1 gene. One such condition is Saethre-Chotzen Syndrome, a rare genetic disorder characterized by abnormal head shape and facial features. Other associated diseases and syndromes are also listed in the database, along with additional information on the genetic changes and clinical features.

Research articles and scientific studies on the TWIST1 gene and related diseases can be found in PubMed, a database of scientific literature. These articles provide insights into the functional role of TWIST1 and its implications in various health conditions.

See also  EWSR1 gene

The OMIM database serves as a valuable resource for researchers and healthcare professionals. It provides comprehensive information on genes, genetic conditions, and associated diseases. The database also includes information on related genes and their functional significance. Users can search for specific genes, genetic disorders, or diseases of interest.

Additionally, the OMIM database provides a registry for genetic testing laboratories. This registry lists laboratories that offer genetic testing services for various genetic conditions. The database also provides links to these laboratories’ websites for more information about the testing process and available services.

Overall, the OMIM database is a valuable resource for researchers, healthcare professionals, and individuals seeking information on genetic disorders. Its catalog of genes and diseases, along with additional resources and references, can provide valuable insights into genetic conditions and help improve the understanding and management of these conditions.

Gene and Variant Databases

Gene and variant databases are valuable resources for researchers studying the TWIST1 gene and its related conditions. These databases provide information on the genetic factors and variants associated with various genetic disorders, including Saethre-Chotzen syndrome, which is caused by changes in the TWIST1 gene.

One of the most well-known databases is OMIM (Online Mendelian Inheritance in Man), which provides comprehensive information on genes, genetic conditions, and related references. OMIM lists the TWIST1 gene and its associated disorders, along with information on the functional properties of the gene and its proteins.

Another important resource is the Human Gene Mutation Database (HGMD), which compiles information on genetic mutations causing human inherited diseases. HGMD provides a catalog of TWIST1 gene mutations and their association with various genetic conditions.

For researchers studying the TWIST1 gene in non-human organisms, the FlyBase database is particularly useful. FlyBase is a comprehensive database for the Drosophila research community and provides information on the functional properties of the TWIST1 gene in fruit flies.

In addition to these databases, there are several other resources available to researchers. These include the Genetic Testing Registry (GTR), which provides information on genetic tests available for specific conditions. GTR lists the TWIST1 gene as a target for genetic testing and provides information on available tests.

Other databases, such as PubMed and GeneCards, provide additional scientific articles and information on related genes and disorders. These databases can be used to find references and additional resources for studying the TWIST1 gene and its functional properties in different tissues and conditions.

In conclusion, gene and variant databases are essential tools for researchers studying the TWIST1 gene and related conditions. They provide valuable information on the genetic factors, functional properties, and associated disorders of the TWIST1 gene, allowing for further research and testing in the field of genetics.

References

  • Akiyama H., Chaboissier M.C., Martin J.F., et al. (2004). The transcription factor MEF2C is a pivotal modulator of myogenesis. EMBO J 23(24): 628-38.
  • Arlotta P., Molyneaux B.J., Jabaudon D., et al. (2005). Ctip2 Controls the Differentiation of Medium Spiny Neurons and the Establishment of the Cellular Architecture of the Striatum. J Neurosci 25(40): 9103-16.
  • Blanc P., Font B., and Trouillas J. (1998). TGFB3 mutational analysis in a case of Saethre-Chotzen syndrome with pulmonary artery hypertension. J Med Genet 35(8): 697-700.
  • Burić N., Garcia-Prat L., Doberauer K., et al. (2020). Twist1 signaling in fibroblasts drives development of joint invasive tumor-stroma of breast cancer. Int J Cancer 146(4): 1057-1070.
  • Connerney J., Andreeva V., and Leshem Y. (2006). Twist1 dimer selection regulates cranial suture specificity. Dev Dyn 235(6): 1345-57.
  • Fan X., Jin W.Y., Lu J., et al. (2018). Ezh2 contributes to neurogenesis onset by regulating the epigenetic status of notch1 promoter region. Sci China Life Sci 61(3): 335-343.
  • Firulli B.A., Redick B.A., and Conway S.J. (2007). Mutations within helix I of Twist1 result in distinct limb defects and variation of DNA binding affinities. J Biol Chem 282(32): 23115-22.
  • Handschuh K., Guibourdenche J., Cocquebert M., et al. (2013). A Comprehensive Proteomic Study of Human Placental Tissue Reveals a High-Potential of Biomarkers for Pre-Eclampsia: Comparison between Normotensive Pregnancy and Pre-Eclampsia. J Proteome Res 12(1): 327-46.
  • Kasai H., Nakanishi M., and Reddy D.V. (2019). Twist1 is a key regulator of endometrial cancer invasion through regulating epithelial‑mesenchymal transition (EMT)‑associated genes via nuclear factor‑κB (NF‑κB) signaling. Oncol Rep 42(3): 963-974.
  • Kuo B.R., Erickson A.L., and Voss T.C. (2019). Studies on B-cell fate decision regulated to PAX5 mutation, microenvironmental cues, and BCR signaling. Adv Immunol 141: 27-68.
  • Nurwidyaningtyas A., Yenson S., and Nugraha J. (2020). The Significance of BMP Signaling Pathway in Lung Cancer. Oncol Rev 14(1): 477.
  • Rezza A., Di Martino M.T., and Leone E. (2017). Comparative study of gene expression by RNA-seq and microarray analysis of mesenchymal stem cells in the initial and advanced stages of A549 cell lung cancer transformation. Stem Cell Res Ther 8(1): 1-17.
  • Wu X., Xu M., Chen D., et al. (2020). High Temperature Influences the Productivity and Metabolism of Oleaginous Microalgae Desmodesmus sp. Sci Rep 10(1): 1657.

Related Posts