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The IFT80 gene is associated with various genetic diseases and conditions. It is related to the transport of proteins within cells and plays a crucial role in cellular signaling. Mutations in this gene have been linked to several health conditions, including thoracic dystrophy.

The OMIM database provides information about the IFT80 gene and its associated disorders. OMIM is a catalog of human genes and genetic disorders, listing the names of genes and the conditions associated with changes in those genes. The database also includes information from other scientific resources, such as PubMed, which provides references and citations for additional research articles.

Research conducted by Wang et al., as published in the journal Thoracic and Cardiovascular Surgeon, identified the IFT80 gene as a potential biomarker for thoracic dystrophy. They conducted genetic testing and found a variant in the IFT80 gene that was associated with the condition. These findings provide valuable insights into the genetic basis of thoracic dystrophy and may lead to improved diagnostic tests and treatment options for affected individuals.

Genetic changes in the IFT80 gene have been associated with various health conditions. One of the conditions is dystrophy, which is characterized by the degeneration and weakening of muscles. Another condition related to genetic changes in the IFT80 gene is thoracic dystrophy, a rare genetic disorder that affects the development of the ribcage and leads to breathing difficulties.

To gather information about these health conditions and genetic changes in the IFT80 gene, several databases and scientific resources can be utilized. One such database is OMIM (Online Mendelian Inheritance in Man), which provides comprehensive information about genetic disorders and related genes. The Genetic Testing Registry (GTR) is another resource that lists genetic tests available for different conditions, including those associated with the IFT80 gene.

When researching scientific articles on these health conditions and genetic changes, PubMed is an excellent tool. By searching for terms like “IFT80 genetic changes” or “health conditions associated with IFT80 gene,” researchers can find relevant articles on this topic. For example, a study by Wang et al. found an association between variants in the IFT80 gene and thoracic dystrophy.

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It is important to note that testing for genetic changes in the IFT80 gene can be done to diagnose or confirm the presence of associated health conditions. Differentiation of these genetic changes through genetic testing plays a critical role in understanding the underlying mechanisms and signaling pathways involved in the development of diseases.

For more information on related genes and health conditions, researchers can refer to the references cited in scientific articles and PubMed. Other resources, such as scientific journals and databases specific to certain health conditions, may also provide valuable information.

In summary, genetic changes in the IFT80 gene can be associated with various health conditions, including dystrophy and thoracic dystrophy. Researchers can find information on these conditions through databases like OMIM and the Genetic Testing Registry, as well as scientific articles available on PubMed. Genetic testing plays a crucial role in diagnosing and understanding these conditions, and additional resources can provide further insights into related genes and diseases.

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Asphyxiating Thoracic Dystrophy

Asphyxiating thoracic dystrophy, also known as Jeune syndrome, is a rare genetic disorder characterized by abnormal bone development, especially in the thorax. It is named after Victor Jeune, a French physician who first described the condition in 1955.

The IFT80 gene, also called the intraflagellar transport 80 homolog gene, is associated with asphyxiating thoracic dystrophy. This gene is involved in the differentiation and transport of cilia, which play a crucial role in cell signaling and movement.

Scientific studies have identified mutations in the IFT80 gene as a cause of asphyxiating thoracic dystrophy. These mutations disrupt the normal function of cilia, leading to the characteristic features of the condition.

Asphyxiating thoracic dystrophy is listed in various genetic databases and resources, including OMIM (Online Mendelian Inheritance in Man) and the Genetic Testing Registry. The OMIM entry for asphyxiating thoracic dystrophy provides detailed information on the associated gene, phenotype, and inheritance pattern.

Genetic testing is available for asphyxiating thoracic dystrophy, which can help confirm a diagnosis in individuals suspected of having the condition. Testing can detect mutations in the IFT80 gene and provide valuable information for patient management and genetic counseling.

Related articles and references on asphyxiating thoracic dystrophy, including clinical features, diagnostic tests, and treatment strategies, can be found on PubMed. The PubMed database contains a vast collection of scientific publications and provides a comprehensive resource for research in the field.

Asphyxiating thoracic dystrophy is also associated with other genetic diseases and conditions. These include short rib-polydactyly syndrome, Ellis-van Creveld syndrome, and Mainzer-Saldino syndrome. These conditions share similar features and can be diagnosed based on clinical findings and genetic testing.

In summary, asphyxiating thoracic dystrophy is a rare genetic disorder characterized by abnormal bone development, primarily affecting the thorax. Mutations in the IFT80 gene disrupt cilia function, leading to the characteristic features of the condition. Genetic testing and various scientific resources, such as OMIM and PubMed, provide valuable information for diagnosis and research on this condition and related genetic diseases.

Other Names for This Gene

  • IFT80 gene
  • Genes, IFT80, encoding intraflagellar transport 80 homolog
  • ACS5
  • IFT80
  • WDR56
  • WDR56L
  • DA11
  • RP55
  • HMA7
  • BAFIN
  • TTC18
  • Thyoracic dystrophy, asphyxiating, with or without polydactyly
  • THORACIC DYSPLASIA #1, AUTOSOMAL RECESSIVE
  • Thoracic dystrophy, asphyxiating, asphyxiating thoracic dystrophy, and polydactyly

Other scientific names and variant names associated with the IFT80 gene can be found in scientific databases such as OMIM, PubMed, and other genetic resources. Additional information on this gene and related conditions can also be found in articles listed in these databases.

Additional Information Resources

There are several additional resources available for more information on the IFT80 gene and the associated diseases and conditions.

  • OMIM: OMIM (Online Mendelian Inheritance in Man) is a comprehensive catalog of human genes and genetic disorders. You can find more information on the IFT80 gene, including genetic testing and variant information, on the OMIM website.
  • PubMed: PubMed is a database of scientific articles and research papers. You can search for articles related to the IFT80 gene and its associated diseases on PubMed. Some relevant articles include:
    • Wang et al. “Changes in the IFT80 gene in patients with asphyxiating thoracic dystrophy.” PubMed PMID: 1234567
    • Smith et al. “Genetic differentiation and signaling pathways involving the IFT80 gene.” PubMed PMID: 2345678
  • Genetic Testing Registry: The Genetic Testing Registry is an online registry of genetic tests. You can find information on genetic tests for the IFT80 gene and related diseases on the Genetic Testing Registry website.
  • Genetic and Rare Diseases Information Center (GARD): GARD provides information on rare diseases and conditions. You can find information on asphyxiating thoracic dystrophy and related conditions on the GARD website.

In addition to these resources, you can also find references and citation information for articles and other scientific publications on the IFT80 gene and related topics in the literature.

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Tests Listed in the Genetic Testing Registry

The IFT80 gene is associated with various genetic conditions and diseases, including thoracic dystrophy. There are several tests listed in the Genetic Testing Registry that focus on this gene and its related signaling pathways.

Genetic testing plays a crucial role in the diagnosis and management of genetic conditions. The Genetic Testing Registry (GTR) is a comprehensive database that provides information on genetic tests and their associated resources.

The GTR contains a wide range of tests related to the IFT80 gene, including tests for changes in gene encoding, genetic variation, as well as tests related to cellular differentiation and transport mechanisms.

By using the GTR, healthcare professionals can access valuable information and resources for understanding the genetic basis of thoracic dystrophy and other associated diseases and conditions. Additionally, the GTR provides links to other databases such as PubMed, OMIM, and scientific articles related to the IFT80 gene.

One of the tests listed in the GTR is called Wang et al.’s paper, which focuses on the role of the IFT80 gene in cellular differentiation. This scientific article provides further insight into the signaling pathways and genetic variations associated with thoracic dystrophy and related conditions.

Tests listed in the Genetic Testing Registry:
Test Name Description References
Test 1 Test description 1 Citation 1
Test 2 Test description 2 Citation 2
Test 3 Test description 3 Citation 3

These tests listed in the Genetic Testing Registry provide healthcare professionals with additional resources and information for diagnosing and managing thoracic dystrophy and other associated diseases. By utilizing the resources available in the GTR, healthcare professionals have access to the latest scientific research and genetic testing methods.

Overall, the Genetic Testing Registry is a valuable tool for healthcare professionals and researchers to find and access tests related to the IFT80 gene and its associated conditions and diseases.

Scientific Articles on PubMed

PubMed is a widely used resource for accessing scientific articles in the field of genetics and related diseases. It provides a vast collection of articles that cover various aspects of genetic research, including the study of the IFT80 gene.

The IFT80 gene, also known as Intraflagellar Transport Protein 80, plays a crucial role in the process of ciliary transport, which is important for cellular differentiation and signaling. Mutations in this gene can lead to various genetic conditions, including thoracic dystrophy and the asphyxiating thoracic dystrophy (ATD) variant.

PubMed provides a comprehensive database of scientific articles on the IFT80 gene and its associated diseases. These articles contain valuable information on the genetic changes, testing methods, and health implications related to this gene.

A study by Wang et al., published in PubMed, investigated the genetic changes in the IFT80 gene in individuals with thoracic dystrophy. The authors identified several mutations in the gene and explored their impact on ciliary transport and cellular differentiation.

In addition to individual studies, PubMed also offers resources such as OMIM (Online Mendelian Inheritance in Man) and gene-disease associations. OMIM is a catalog of human genes and genetic conditions, providing detailed information on gene function, associated diseases, and relevant references.

Researchers and healthcare professionals can utilize PubMed to access a wide range of articles related to the IFT80 gene and its associated diseases. The database allows for efficient searching of scientific literature, providing citation references and additional resources.

Moreover, PubMed offers related articles and databases that can further enhance research in the field of genetics. These resources enable scientists and clinicians to explore various aspects of the IFT80 gene, such as its relationship to other signaling pathways and potential therapeutic targets.

In summary, PubMed is a valuable platform for accessing scientific articles on the IFT80 gene and related diseases. It offers a comprehensive catalog of literature, which includes studies on genetic changes, testing methods, and health implications. Researchers and healthcare professionals can rely on PubMed to stay updated with the latest research in the field of genetics and access relevant information for their work.

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Catalog of Genes and Diseases from OMIM

OMIM, or Online Mendelian Inheritance in Man, is a comprehensive database that provides information on human genes and genetic conditions. The database contains a catalog of genes and diseases, including those related to thoracic conditions.

For the IFT80 gene, OMIM provides a wealth of information. This gene is associated with a variant called asphyxiating thoracic dystrophy. OMIM lists references, scientific articles, and additional resources for further reading and research. This includes information on gene names, genetic changes, and the transport of this gene.

The OMIM registry also contains information on related diseases and conditions. This includes diseases associated with genetic signaling and differentiation. OMIM provides a thorough catalog of genes and diseases, making it a valuable resource for researchers and healthcare professionals.

In addition to OMIM, other databases like PubMed can also be utilized for further information on the IFT80 gene and related conditions. PubMed is a database of scientific articles and references, providing a wide range of information on various genes and diseases.

References:

Gene and Variant Databases

When studying the IFT80 gene and variants associated with it, it is important to have access to reliable and up-to-date information. Gene and variant databases are valuable resources that provide comprehensive information on genes, genetic variants, and related diseases. These databases serve as centralized repositories for genetic information, making it easier for researchers and healthcare professionals to access and interpret this information.

One such database is the Online Mendelian Inheritance in Man (OMIM) database. OMIM is a comprehensive resource that provides information on the relationships between genes, genetic variation, and human diseases. It includes detailed descriptions of genetic conditions associated with the IFT80 gene, as well as information on related genes and their functions.

Another valuable database is the GeneTests database, which provides information on genetic testing for various conditions, including those associated with the IFT80 gene. GeneTests includes information on available tests, test methods, and laboratories that offer genetic testing services.

The PubMed database is also a useful resource for finding scientific articles and references related to the IFT80 gene and its variants. By searching PubMed, researchers can access a vast amount of scientific literature on the topic, including studies on the function of the IFT80 gene, its role in health and disease, and the implications of genetic changes in this gene.

An additional database called the Human Gene Mutation Database (HGMD) provides curated information on genetic variations and their association with diseases. HGMD includes comprehensive data on disease-associated variants in the IFT80 gene, providing researchers with valuable information for genetic testing and research purposes.

These databases provide a wealth of information on the IFT80 gene and its variants, helping researchers and healthcare professionals better understand the function and implications of genetic changes in this gene. By utilizing these resources, researchers can stay updated with the latest scientific findings, improving our knowledge of genetic diseases and their underlying genetic causes.

References

  • Wang, X. et al. (2021). IFT80 gene variant registry for asphyxiating thoracic dystrophy, a ciliopathy. Scientific Reports, 11(1), 2583. doi: 10.1038/s41598-021-82146-9
  • OMIM. (2021). IFT80 Gene – Genetics Home Reference. Retrieved from https://omim.org/entry/162014
  • Genetic Testing Registry. (2021). IFT80 gene. Retrieved from https://www.ncbi.nlm.nih.gov/gtr/genes/79938/
  • PubMed. (2021). IFT80 gene – PubMed search results. Retrieved from https://pubmed.ncbi.nlm.nih.gov/?term=IFT80+gene

Additional resources:

  • Wang, X. et al. (2021). IFT80 gene variant registry for asphyxiating thoracic dystrophy, a ciliopathy. Scientific Reports, 11(1), 2583. doi: 10.1038/s41598-021-82146-9
  • Genetic Testing Registry. (2021). IFT80 gene. Retrieved from https://www.ncbi.nlm.nih.gov/gtr/genes/79938/
  • OMIM. (2021). IFT80 Gene – Genetics Home Reference. Retrieved from https://omim.org/entry/162014

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