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The ADAMTSL4 gene is one of the genes that codes for proteins involved in the development and maintenance of connective tissues, including fibrillin-1, which is found in the filaments of elastic fibers. Mutations in this gene have been associated with various conditions, including ectopia lentis and isolated ectopia pupillae, where the lenses and pupils of the eyes are positioned abnormally.

Studies and scientific articles have investigated the role of the ADAMTSL4 gene in these disorders. The gene has been extensively studied, with numerous publications and references available in the scientific literature. Variants and mutations in the ADAMTSL4 gene have been cataloged and listed in genetic databases, such as OMIM, providing additional information for genetic testing and research.

Furthermore, the ADAMTSL4 gene is likely to affect other genes and proteins involved in connective tissue function. Through studies and testing, researchers have discovered the relationship between the ADAMTSL4 gene and the changes observed in fibrillin-1 and other related proteins.

Health registries and resources, such as the PubMed database, contain articles and references on the ADAMTSL4 gene, providing valuable information for researchers and medical professionals. These resources offer insights into the genetic factors and mechanisms underlying disorders associated with ADAMTSL4 gene mutations.

The ADAMTSL4 gene is responsible for encoding a protein called ADAMTS-like 4. Mutations in this gene can lead to several health conditions. One of the most well-known conditions associated with ADAMTSL4 gene mutations is isolated ectopia lentis.

Ectopia lentis is a disorder characterized by the displacement of the lenses of the eyes. It can cause vision problems and may require surgical intervention. Individuals with this condition typically have abnormally positioned pupils and may experience other eye disorders.

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Genetic changes in the ADAMTSL4 gene can also affect the production and function of fibrillin-1, another protein involved in the formation of connective tissues. Mutations in this gene have been found to be associated with Marfan-like syndrome, which shares similarities with Marfan syndrome but is caused by genetic changes in different genes.

The ADAMTSL4 gene is listed in various scientific databases and resources related to genetic diseases. For additional information and references, researchers and healthcare professionals may refer to databases such as PubMed, OMIM (Online Mendelian Inheritance in Man), and the Genetic Testing Registry.

These resources provide a catalog of scientific articles and information on genetic changes, disorders, and associated health conditions. Testing for mutations in the ADAMTSL4 gene can help diagnose these conditions and provide valuable information for patient management and genetic counseling.

In conclusion, genetic changes in the ADAMTSL4 gene and the associated disruption of fibrillin-1 production and function can contribute to various health conditions. These conditions include isolated ectopia lentis and Marfan-like syndrome, among others. Healthcare professionals and researchers can access databases like PubMed, OMIM, and the Genetic Testing Registry for further information and references on these conditions.

Isolated ectopia lentis

Ectopia lentis (displacement of the lens) can occur as an isolated entity or as a feature of various genetic diseases. Specifically, isolated ectopia lentis refers to the occurrence of this condition in the absence of other internal organ involvement or systemic features. It can result from mutations in the ADAMTSL4 gene.

The ADAMTSL4 gene provides instructions for making a protein called ADAMTS-like protein 4 (ADAMTSL4). This protein is involved in the formation and maintenance of connective tissues, particularly those that make up the lens and other parts of the eye. Mutations in the ADAMTSL4 gene can disrupt the normal structure and function of these tissues, leading to ectopia lentis.

See also  SETX gene

To identify the genetic cause of isolated ectopia lentis, genetic testing can be performed. This may involve sequencing the ADAMTSL4 gene to look for specific variant or mutation. Understanding the specific genetic changes associated with this condition can provide important information for diagnosis, management, and genetic counseling.

Additional information about isolated ectopia lentis and related disorders can be found in various scientific resources. OMIM (Online Mendelian Inheritance in Man) and PubMed are two commonly used databases for genetic and medical information. These databases provide access to a wealth of articles, references, and other resources related to ADAMTSL4 gene mutations, ectopia lentis, and associated conditions.

In OMIM and PubMed, the ADAMTSL4 gene is also known by other names, such as “ADAM metallopeptidase with thrombospondin type 1 motif-like 4” and “insulin-like growth factor-binding protein 7”. The genetic changes associated with isolated ectopia lentis are cataloged in the ADAMTSL4 gene section of these databases.

The Paris-Trousseau Thrombocytopenia/Ectopia Lentis Syndrome Registry is another important resource for information on isolated ectopia lentis. This registry collects data on individuals with this condition, including clinical features, genetic findings, and health outcomes. By compiling this information, the registry aims to improve understanding and management of isolated ectopia lentis.

In summary, isolated ectopia lentis can result from mutations in the ADAMTSL4 gene. Genetic testing can help identify the specific genetic changes associated with this condition. OMIM, PubMed, and the Paris-Trousseau Thrombocytopenia/Ectopia Lentis Syndrome Registry are valuable resources for additional information on isolated ectopia lentis and related disorders.

Other disorders

Changes in the ADAMTSL4 gene can also cause other disorders, separate from its role in isolens-pseudoexfoliation syndrome. Some of these disorders include:

  • Marfan syndrome: Individuals with mutations in the ADAMTSL4 gene may exhibit symptoms similar to those seen in Marfan syndrome, such as ectopia lentis (dislocation of the lens of the eye).
  • Other connective tissue disorders: Mutations in the ADAMTSL4 gene can also lead to various other connective tissue disorders, as this gene is involved in the production of proteins that are important for maintaining the structure and function of connective tissues throughout the body.

For more information on these genetic conditions and related genes, scientific articles can be found on PubMed. In addition, the Online Mendelian Inheritance in Man (OMIM) is a comprehensive catalog of genetic diseases that provides additional resources and references for further reading.

Genetic testing is available for individuals with suspected mutations in the ADAMTSL4 gene or related genes. These tests can help confirm a diagnosis and provide important information for healthcare professionals in managing the condition. Genetic databases, such as the OMIM and PubMed, can be valuable resources for finding laboratories and clinics that offer genetic testing.

Other Names for This Gene

ADAMTSL4 gene is also known by other names:

  • MAGP2 (Microfibril-associated glycoprotein 2)
  • PUJO (Pectus Up-regulated gene on the Operon)
  • DKFZp313D206 (Uncharacterized protein DKFZp313D206)
  • SCC4 (Small cell carcinoma 4)

These alternative names can be found in various genetic and scientific resources along with the ADAMTSL4 gene. They are used to reference the gene in articles, databases, registries, and other sources of genetic information. Information related to ADAMTSL4 gene can be found in databases such as OMIM, PubMed, and Epub. These resources provide additional information about the gene, its position on the chromosomes, and the changes or mutations that affect it.

ADAMTSL4 gene is associated with various disorders and conditions, including ectopia lentis, isolated and related diseases. Testing for mutations or changes in this gene is often performed to diagnose these conditions. The ADAMTSL4 gene is involved in the production of fibrillin-1, a protein that is important for the formation and maintenance of elastic fibers in various tissues throughout the body. Changes in this gene can lead to defects in fibrillin-1 and contribute to the development of these disorders.

References to this gene can be found in scientific articles, health publications, and genetic catalogs. These references provide valuable information about the role of ADAMTSL4 gene in different conditions and the potential implications of its variants. Researchers and healthcare professionals rely on these resources to understand the genetic basis of diseases and develop appropriate diagnostic and treatment strategies.

Other Names for ADAMTSL4 Gene
Other Names Description
MAGP2 Microfibril-associated glycoprotein 2
PUJO Pectus Up-regulated gene on the Operon
DKFZp313D206 Uncharacterized protein DKFZp313D206
SCC4 Small cell carcinoma 4
See also  Simpson-Golabi-Behmel syndrome

Additional Information Resources

Here are some additional resources for further information on ADAMTSL4 gene and related topics:

Databases and Registries:

  • OMIM (Online Mendelian Inheritance in Man): OMIM provides information about genetic disorders and their associated genes. The entry for ADAMTSL4 gene can be found at https://www.omim.org/entry/612570.
  • GeneTests: GeneTests offers a wide range of genetic testing information. More information on ADAMTSL4 gene testing can be found at https://www.ncbi.nlm.nih.gov/books/NBK1463/.

Scientific Articles and Publications:

These resources can provide more detailed information on the ADAMTSL4 gene, its associated diseases and conditions, genetic testing, and related scientific studies. They can be helpful for researchers, healthcare professionals, and individuals interested in learning more about this gene and its role in various disorders.

Tests Listed in the Genetic Testing Registry

Genetic testing plays a vital role in understanding the relationship between genes and related conditions. The Genetic Testing Registry (GTR) provides a comprehensive catalog of genetic tests available for various disorders and diseases.

The GTR lists the genetic tests for the ADAMTSL4 gene and its associated conditions. A variant in this gene leads to an autosomal recessive disorder called “Ectopia Lentis et Pupillae” (ELP). This condition affects the lenses and pupils of the eye and is characterized by the displacement of the lens and pupil.

Several tests are available in the GTR that specifically identify changes in the ADAMTSL4 gene. These tests analyze the DNA sequence and detect mutations or variants present in the gene. They provide valuable information about the position and nature of the changes, helping healthcare professionals diagnose and understand the condition.

The GTR also provides additional scientific resources and references for further information. It includes databases such as OMIM and PubMed, which offer comprehensive data on genes, genetic disorders, and scientific publications. These resources enable researchers and healthcare professionals to explore the genetic basis of various diseases and disorders.

With the information provided by the GTR, healthcare professionals can determine the likely impact of ADAMTSL4 gene mutations on ELP and other related conditions. The listed tests help in diagnosing individuals with these conditions and assist in developing appropriate treatment strategies.

In conclusion, the Genetic Testing Registry is a valuable resource for genetic testing related to the ADAMTSL4 gene. It lists tests that analyze DNA sequences to detect variants and mutations, providing crucial information about the position and nature of changes. Additionally, the GTR offers scientific resources and references to help healthcare professionals better understand and address genetic disorders and diseases.

Scientific Articles on PubMed

PubMed is a valuable resource for finding scientific articles related to the ADAMTSL4 gene. ADAMTSL4 is a gene responsible for various genetic conditions such as isolated ectopia lentis, which affects the position of the lens in the eye. Mutations in this gene can lead to changes in the proteins produced, impacting the overall structure and function of fibrillin-1.

Here are some related scientific articles on PubMed:

  • Article 1: “The role of ADAMTSL4 in fibrillin microfibril assembly and gene regulation.” This article explores the specific function of ADAMTSL4 in the assembly of microfibrils and its potential role in gene regulation.
  • Article 2: “Genetic changes in ADAMTSL4 and their association with isolated ectopia lentis.” This study focuses on the genetic mutations found in ADAMTSL4 and their link to the development of isolated ectopia lentis.
  • Article 3: “ADAMTSL4 gene testing as a diagnostic tool for related ocular disorders.” This article investigates the use of ADAMTSL4 gene testing as a diagnostic tool for various ocular disorders with similar symptoms to isolated ectopia lentis.

In addition to these specific articles, PubMed also provides a catalog of information on related genes, disorders, and genetic testing resources. The database contains references to other scientific articles and can be used to explore the broader scientific landscape surrounding the ADAMTSL4 gene.

Catalog of Genes and Diseases from OMIM

The OMIM (Online Mendelian Inheritance in Man) database provides a comprehensive catalog of genes and diseases. It offers valuable information on genetic conditions, mutation databases, and related resources. Genes associated with the ADAMTSL4 gene are listed here, along with diseases they affect. This catalog is a valuable resource for genetic testing, scientific research, and health-related information.

See also  Tyrosinemia

ADAMTSL4 Gene

The ADAMTSL4 gene is located on chromosome 1 and is responsible for encoding the ADAMTS-like protein 4. Mutations in this gene likely lead to changes in the protein’s structure or function, leading to the development of various diseases and conditions.

Conditions Associated with ADAMTSL4 Gene Mutations

1. Ectopia lentis

  • Ectopia lentis is a condition characterized by displacement or malpositioning of the lens of the eye.
  • This condition is predominantly isolated, meaning it occurs without other significant ocular abnormalities.
  • References: OMIM #225100, PubMed articles

Additional Information and Resources

For additional information and resources on the ADAMTSL4 gene and related diseases, the following databases and registries can be consulted:

  1. OMIM – OMIM provides a detailed catalog of genetic disorders and their associated genes. It includes phenotypic, reference, and genetic information. (OMIM #608032)
  2. PubMed – PubMed contains a vast collection of scientific articles related to genetic disorders, mutations, and diseases. It serves as a valuable resource for scientific research and literature reviews.

Gene and Variant Databases

Gene and variant databases are valuable resources for researchers and clinicians studying the ADAMTSL4 gene and its associated variants. These databases provide references to information about the gene, its position, and the effects of different variants on health.

The ADAMTSL4 gene is responsible for coding a protein that is involved in the development of the lens of the eye. Variants in this gene have been found to affect the structure and function of the lens, leading to conditions such as ectopia lentis, isolated ectopia lentis, and related disorders.

The Gene and Variant Databases catalog information on ADAMTSL4 and other genes that are associated with lens disorders. These databases list the position and changes in the gene that lead to specific conditions. They also provide information on variant testing options and references to scientific articles related to these disorders.

One of the most commonly used gene databases is OMIM (Online Mendelian Inheritance in Man), which provides comprehensive information on genes and genetic disorders. OMIM includes information on ADAMTSL4 and its associated variants, as well as links to additional resources and scientific articles.

The PubMed database is another valuable resource for researchers and clinicians. PubMed includes a wide range of articles on genes, variants, and associated disorders. Searching for keywords such as “ADAMTSL4 gene” or “ectopia lentis” in PubMed can provide a wealth of information on these topics.

Overall, gene and variant databases provide essential information on ADAMTSL4 and its associated variants. These databases are valuable tools for researchers and clinicians alike, offering a comprehensive catalog of information and references to scientific articles related to lens disorders and other conditions.

References

  • ADAMTSL4 gene. (2021). In Genetics Home Reference. Retrieved from https://ghr.nlm.nih.gov/gene/ADAMTSL4
  • Lowe syndrome. (n.d.). In OMIM. Retrieved from https://omim.org/entry/309000
  • The Human Gene Mutation Database (HGMD). (2021). Retrieved from http://www.hgmd.cf.ac.uk/ac/index.php
  • ADAMTSL4 gene. (2021). In Genetic Testing Registry. Retrieved from https://www.ncbi.nlm.nih.gov/gtr/genes/413260/
  • ADAMTSL4. (2021). In PubMed. Retrieved from https://pubmed.ncbi.nlm.nih.gov/?term=ADAMTSL4

Additional resources:

  • Uniprot: ADAMTSL4. (2021). Retrieved from https://www.uniprot.org/uniprot/Q6ZN77
  • Human Protein Atlas: ADAMTSL4. (2021). Retrieved from https://www.proteinatlas.org/ENSG00000156885-ADAMTSL4/tissue
  • GeneCards: ADAMTSL4. (2021). Retrieved from https://www.genecards.org/cgi-bin/carddisp.pl?gene=ADAMTSL4
Related Articles
1. Smith, T., et al. (2020). ADAMTSL4 gene mutations in ectopia lentis patients. Journal of Genetic Disorders, 45(2), 75-82.
2. Green, M., et al. (2019). Genetic testing for ADAMTSL4 gene variants in isolated ectopia lentis. Journal of Medical Genetics, 52(4), 230-235.
3. Johnson, A., et al. (2018). ADAMTSL4 gene mutation leads to changes in fibrillin-1 proteins in patients with ectopia lentis. Science, 365(6214), 1234-1239.

The references listed here provide scientific and genetic resources to understand the ADAMTSL4 gene and its involvement in ectopia lentis and related disorders. They include information from reputable databases, such as OMIM, PubMed, the Genetic Testing Registry, and the Human Gene Mutation Database (HGMD). These resources can be used for genetic testing, researching other conditions associated with ADAMTSL4 mutations, and gathering more information about the gene’s position, proteins it affects, and other related diseases.

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