Contents
[hide]
[show]

The OXCT1 gene encodes the mitochondrial enzyme 3-oxoacid CoA-transferase 1, also known as succinyl-CoA:3-ketoacid CoA-transferase (SCOT). This enzyme is responsible for the final step in the production of ketone bodies, which are important for energy production during periods of fasting or prolonged exercise.

Deficiency of the OXCT1 gene leads to a severe metabolic disorder called SCOT deficiency. This condition is characterized by a buildup of toxic compounds and a decrease in the production of ketone bodies. Symptoms can include seizures, developmental delay, hypotonia, and metabolic acidosis.

Testing for OXCT1 gene mutations can be done through genetic testing laboratories, and results can be used to confirm a diagnosis of SCOT deficiency. The OXCT1 gene is listed in various genetic databases and resources, including the OMIM database, which provides detailed information on the gene, associated diseases, and genetic changes.

Scientific articles and references related to the OXCT1 gene can be found on PubMed and other scientific databases. Additional information and resources for patients and healthcare professionals can be found on the registry for severe genetic developmental disorders, known as the KONDO gene repository. The KONDO gene registry provides a catalog of genetic variants and related genes, as well as information on diagnostic tests and available treatments for genetic disorders.

Genetic changes in the OXCT1 gene can result in various health conditions. These changes can be cataloged and listed in databases and registries dedicated to genetic diseases. When testing for certain severe health conditions, genetic testing for succinyl-CoA 3-ketoacid CoA transferase deficiency may be recommended.

Genetic changes in the OXCT1 gene have been found to be related to succinyl-CoA 3-ketoacid CoA transferase deficiency. This deficiency can cause significant health problems and is characterized by the inability of the body to break down certain fatty acids. Individuals with this deficiency may experience symptoms such as developmental delays, intellectual disability, muscle weakness, and seizures.

Pre-tax flexible spending accounts (FSAs) are often touted as the answer to high out-of-pocket medical costs, but many FSAs have “use it or lose it” rules. FSA holders lose $50 to $100 per year on average, CBS News reported, but since you’re allowed to contribute up to $2,650, you could risk losing thousands of dollars if you don’t spend your FSA money in time.

Additional information on health conditions related to genetic changes in the OXCT1 gene can be found in various resources such as PubMed, OMIM, and other genetic databases. These resources provide references, articles, and variant information on the genes and conditions related to genetic changes in the OXCT1 gene.

One such study by Kursula et al. (2019) investigated a variant in the OXCT1 gene and its association with succinyl-CoA 3-ketoacid CoA transferase deficiency. The study provided insights into the genetic basis of the condition and potential therapeutic approaches.

References and Resources
Resource Website
PubMed pubmed.ncbi.nlm.nih.gov
OMIM www.omim.org
Genetic databases Various databases provide information on genetic diseases and gene variants.

By utilizing these resources, researchers and healthcare professionals can stay updated on the latest research and developments regarding genetic changes in the OXCT1 gene and the associated health conditions. This knowledge can contribute to improved diagnosis, management, and potential treatments for individuals affected by succinyl-CoA 3-ketoacid CoA transferase deficiency and other related diseases.

Succinyl-CoA3-ketoacid CoA transferase deficiency

Succinyl-CoA3-ketoacid CoA transferase deficiency, also known as SCOT deficiency, is a rare genetic condition that affects the OXCT1 gene. This gene provides instructions for making an enzyme called succinyl-CoA3-ketoacid CoA transferase, or SCOT. This enzyme is involved in a process called ketone body metabolism, which helps convert certain fats into energy.

SCOT deficiency is inherited in an autosomal recessive manner, meaning that both copies of the OXCT1 gene in each cell must have mutations for an individual to be affected. The severity of the condition can vary, with some individuals experiencing mild symptoms and others having severe complications.

People with SCOT deficiency may experience a range of symptoms, including developmental delay, intellectual disability, seizures, and problems with movement and coordination. These symptoms can be attributed to the impaired energy production caused by the deficiency.

Diagnosis of SCOT deficiency is typically done through genetic testing. This involves analyzing the OXCT1 gene for changes or mutations. Several genetic testing laboratories offer this type of testing, and the results can provide valuable information for individuals and their healthcare providers.

See also  LAMA2 gene

For additional information on SCOT deficiency and related conditions, the following resources may be useful:

  • Online Mendelian Inheritance in Man (OMIM): OMIM is a catalog of human genes and genetic disorders. The OMIM entry for SCOT deficiency (OMIM #245050) provides a detailed summary of the condition, including genetic, clinical, and scientific information.
  • Registry of Genetic Diseases: The Registry of Genetic Diseases is a comprehensive database that contains information on various genetic conditions, including SCOT deficiency. It provides information on the genetic basis of the condition, as well as available diagnostic and treatment options.
  • PubMed: PubMed is a database of scientific articles and research papers. Searching for “succinyl-CoA3-ketoacid CoA transferase deficiency” or other related terms can help you find scientific articles and studies on SCOT deficiency.
  • Scientific articles and references: There are several scientific articles and references available on SCOT deficiency. Some notable articles include “Structural Studies of the SCOT Variant Causing an Atypical Form of Human 3-Methylcrotonyl-CoA Carboxylase Deficiency” by K. Kursula and “Molecular Analysis and Characterization of the Human 3-Methylcrotonyl-CoA Carboxylase Gene” by T. Kondo and L. M. Palmieri. These articles provide insights into the genetic and molecular aspects of SCOT deficiency.

In summary, Succinyl-CoA3-ketoacid CoA transferase deficiency, or SCOT deficiency, is a genetic condition caused by mutations in the OXCT1 gene. It can lead to impaired ketone body metabolism and energy production, resulting in a range of symptoms and complications. Genetic testing, along with resources such as OMIM, the Registry of Genetic Diseases, PubMed, and scientific articles, can provide valuable information and support for individuals and healthcare providers dealing with this condition.

Other Names for This Gene

The OXCT1 gene is also known by other names:

  • SCOT gene: This name stands for succinyl-CoA:3-ketoacid coenzyme A transferase gene. It refers to the protein produced by this gene, which is involved in the breakdown of certain amino acids and fatty acids.
  • OXCT: This abbreviation is often used to refer to the protein produced by the OXCT1 gene.
  • SCO: This is another abbreviation for the protein produced by the OXCT1 gene.

Additional names for this gene include:

  • SCOT: This abbreviation is commonly used to refer to the protein produced by the OXCT1 gene. It is also used to refer to genetic diseases that are caused by changes in this gene.
  • Succinyl-CoA:3-ketoacid CoA transferase: This is the full name of the protein produced by the OXCT1 gene.
  • 3-ketoacid CoA transferase: Another name for the protein produced by the OXCT1 gene.

For additional information on this gene, genetic diseases related to it, and scientific research articles, please refer to the following resources:

  • PubMed: A searchable database of scientific articles.
    • Search for “OXCT1 gene” to find articles specifically about this gene.
  • OMIM: The Online Mendelian Inheritance in Man database, which provides information on genetic conditions and genes.
    • Search for “OXCT1” to find information on genetic diseases related to this gene.
  • GeneTests: A medical genetics information resource with information on genetic testing for various conditions.
    • Search for “OXCT1” to find information on genetic testing for OXCT1 gene deficiency.

References:

  1. Kursula, P., et al. (2002). 3-ketoacyl-CoA thiolase in human health and disease. Int J Biochem Cell Biol 34, 225-249.
  2. Palmieri, L., et al. (2015). Genetic and functional characterization of SCO1: a gene involved in cytochrome c oxidase assembly. Hum Mol Genet 24, 2249-2265.
  3. Kondo, N., et al. (2004). Molecular basis of succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency in a neonate. J Inherit Metab Dis 27, 649-656.

List of Databases and Resources
Database/Resource Description
PubMed A searchable database of scientific articles
OMIM The Online Mendelian Inheritance in Man database
GeneTests A medical genetics information resource

Additional Information Resources

Here are some additional resources for further information on the OXCT1 gene:

  • Scientific Articles: You can find scientific articles related to the OXCT1 gene and its variants by searching in databases such as PubMed.

  • Genetic Testing: If you are interested in genetic testing for OXCT1 gene deficiency or related conditions, you can consult genetic testing providers listed in the Genetic Testing Registry or other health-related databases.

  • OMIM: The Online Mendelian Inheritance in Man (OMIM) database provides detailed information on diseases and genes, including OXCT1 and related conditions.

  • GeneCards: GeneCards is a comprehensive database that provides information about genes, including OXCT1. It contains information on gene function, expression, and related disorders.

  • References: For more specific references on the OXCT1 gene and related research, you can refer to scientific articles and studies cited in the resources mentioned above.

See also  COL6A2 gene

Tests Listed in the Genetic Testing Registry

The Genetic Testing Registry (GTR) is a comprehensive catalog of genetic tests and their associated information. It provides names, descriptions, and other details about genetic tests for a variety of conditions and diseases. The GTR is a valuable resource for healthcare professionals, researchers, and individuals seeking information on genetic testing.

One of the genetic conditions listed in the GTR is succinyl-CoA3-ketoacid coa-transferase deficiency, also known as SCOT deficiency. SCOT deficiency is a severe genetic disorder caused by changes in the OXCT1 gene. This gene provides instructions for making an enzyme called succinyl-CoA3-ketoacid coa-transferase, which is essential for the breakdown of certain fats and proteins in the body.

The GTR lists several tests related to the OXCT1 gene and SCOT deficiency. These tests can identify changes in the OXCT1 gene that are associated with the condition. They can also provide information on the severity of the condition and help guide treatment decisions.

Some of the tests listed in the GTR include:

  • Sequencing of the OXCT1 gene: This test looks for changes in the DNA sequence of the OXCT1 gene. It can identify genetic variants that are associated with SCOT deficiency.
  • Functional analysis of OXCT1 variants: This test assesses the effect of specific genetic variants on the function of the OXCT1 enzyme. It can help determine the severity of SCOT deficiency.
  • Genomic testing for SCOT deficiency: This test uses advanced genomic technologies to analyze the entire OXCT1 gene and other related genes. It can provide a comprehensive evaluation of genetic changes associated with SCOT deficiency.

These tests are conducted by specialized laboratories and require a blood or saliva sample from the individual being tested. The results of these tests can provide valuable information for diagnosis, treatment, and genetic counseling.

In addition to the tests listed in the GTR, there are several scientific articles and resources available on the OXCT1 gene, SCOT deficiency, and related genetic conditions. PubMed, OMIM, and other genetic databases contain references to these articles and provide further information on the genetics, symptoms, and management of SCOT deficiency.

Overall, the Genetic Testing Registry is a valuable tool for healthcare professionals, researchers, and individuals seeking information on genetic testing for SCOT deficiency, as well as other genetic conditions. It provides a comprehensive catalog of tests, scientific articles, and resources related to the OXCT1 gene and its associated conditions.

Scientific Articles on PubMed

When researching the OXCT1 gene, it is important to consult scientific articles available on PubMed. PubMed is a comprehensive database that references articles from various scientific journals.

Scientific articles on PubMed provide valuable information on the OXCT1 gene and its variants. Researchers can find a catalog of articles that discuss the genetic changes and related conditions associated with this gene. These articles can aid in understanding the role of OXCT1 and its impact on health.

One article of interest is “Mutations in the OXCT1 Gene and Severe CoA-Transferase Deficiency” by Palmieri et al. This study explores how genetic changes in the OXCT1 gene lead to severe coA-transferase deficiency, a condition that affects the body’s ability to break down CoA-Succinyl-CoA3-Ketoacid, resulting in metabolic disorders.

Another relevant article is “The OXCT1 Gene and Its Role in Scot Deficiency” by Kondo et al. This study focuses on the genetic variant in the OXCT1 gene that causes Scot deficiency, a disorder characterized by neurological symptoms.

In addition to PubMed, other genetic databases like OMIM can provide additional resources for OXCT1 gene research. These databases contain information on various genetic variants and associated health conditions.

When conducting genetic testing or researching the OXCT1 gene, it is crucial to consult scientific articles to stay updated on the latest findings. Pubmed provides a platform for researchers to access the latest publications in the field.

Here are some articles related to the OXCT1 gene listed on PubMed:

  • Mutations in the OXCT1 Gene and Severe CoA-Transferase Deficiency by Palmieri et al.
  • The OXCT1 Gene and Its Role in Scot Deficiency by Kondo et al.
  • Genetic Changes in the OXCT1 Gene and Metabolic Disorders by Palmieri et al.
  • Characteristics of the OXCT1 Gene in Neurological Disorders by Kursula et al.

By referring to these scientific articles, researchers can gain a comprehensive understanding of the OXCT1 gene and its implications in various diseases. It is important to stay updated with the latest research to improve diagnosis and treatment options for patients.

See also  CYP2C19 gene

Catalog of Genes and Diseases from OMIM

The Catalog of Genes and Diseases from OMIM is a valuable resource for genetic information on a variety of severe conditions. OMIM, or the Online Mendelian Inheritance in Man, is a comprehensive database that provides information on the relationships between genes and genetic disorders.

When a particular gene, in this case the OXCT1 gene, is related to a specific genetic condition, OMIM provides additional information on the disease. For example, if you search for OXCT1 gene in OMIM, you will find information on the genetic changes that can cause OXCT1 gene deficiency.

OMIM also provides a registry of scientific articles and references related to the OXCT1 gene and its associated diseases. This can be particularly useful for researchers and healthcare professionals looking for the latest scientific information on OXCT1 gene deficiency and related conditions.

In addition to OMIM, there are other databases and resources available for genetic testing and information. PubMed is a widely used database that provides access to articles on biomedical topics, including genetic research. Scientific articles related to OXCT1 gene deficiency can be found on PubMed, providing further information on this genetic condition.

Genetic testing for OXCT1 gene deficiency and other genetic conditions is available through various laboratories and health institutions. These tests can help diagnose individuals with OXCT1 gene deficiency and provide information on the severity of the disease and potential treatment options.

In conclusion, the Catalog of Genes and Diseases from OMIM, along with other resources like PubMed and genetic testing laboratories, provides a wealth of information on the OXCT1 gene and its associated diseases. This information is essential for researchers, healthcare professionals, and individuals seeking to learn more about OXCT1 gene deficiency and related conditions.

Gene and Variant Databases

In the field of genetics, gene and variant databases play a crucial role in providing comprehensive information on genes, genetic changes, and related diseases. These databases serve as valuable resources for researchers, healthcare professionals, and individuals seeking information about specific genetic conditions.

One such database is OMIM (Online Mendelian Inheritance in Man) which provides information on genetic conditions and genes. It also includes details on the mode of inheritance, clinical features, and references to scientific articles. OMIM is a reliable source for understanding the genetic basis of diseases and the associated gene variants.

When it comes to testing for genetic conditions related to the OXCT1 gene, the GeneTests.org database provides a registry of laboratories that offer genetic testing services. This database helps healthcare professionals and individuals find testing facilities that specialize in assessing the OXCT1 gene and its variants.

COA-FLUOR goes a step further by supplying a database dedicated to the COA transferase gene. It includes information on specific variants, their clinical significance, and associated diseases. This database is a valuable resource for researchers and healthcare professionals seeking to understand the genetic basis of COA transferase deficiency.

For individuals interested in learning about their own genetic makeup, resources like the National Center for Biotechnology Information’s Genetic Testing Registry (GTR) provide a comprehensive list of labs offering genetic testing. The GTR database includes information on available tests for genes related to various conditions, including the OXCT1 gene.

Additionally, the Human Gene Mutation Database (HGMD) provides curated information on gene variants and their clinical significance. It includes data from scientific articles, with references to support the reported findings. This database is frequently used by researchers and healthcare professionals to gain additional insights into specific gene variants.

References

  • Palmieri M, et al. “Genetic Testing in Rare Diseases: Opportunities and Challenges for the Future.” Int J Mol Sci. 2020 Dec; 21(23): 9168. doi: 10.3390/ijms21239168. PMID: 33255707; PMCID: PMC7731126.

  • Kursula P, et al. “The Structure, Function, and Role of Thiamine Pyrophosphate in Cellular Metabolism.” Subcell Biochem. 2012; 56: 25-64. doi: 10.1007/978-94-007-2199-9_2. PMID: 22116667.

  • Kondo Y, et al. “Structure of Human Succinyl-CoA: 3-Ketoacid CoA-Transferase.” Sci Rep. 2016 Nov; 6: 37232. doi: 10.1038/srep37232. PMID: 27892518; PMCID: PMC5125838.

  • OMIM. “OXCT1 Gene.” Online Mendelian Inheritance in Man, Johns Hopkins University. Accessed April 10, 2022. Available at: https://www.omim.org/entry/245050.

  • PubMed. “OXCT1.” National Library of Medicine. Accessed April 10, 2022. Available at: https://pubmed.ncbi.nlm.nih.gov/?term=OXCT1.

  • Consortium of Glycogen Storage Disease. “OXCT1.” Accessed April 10, 2022. Available at: https://www.boascenter.org/glycogen-storage-disease-scan/gene?disease=KEN_M.

  • Genetic and Rare Diseases Information Center (GARD). “3-Hydroxyacyl-CoA Dehydrogenase Deficiency.” National Center for Advancing Translational Sciences, National Institutes of Health. Accessed April 10, 2022. Available at: https://rarediseases.info.nih.gov/diseases/7886/3-hydroxyacyl-coa-dehydrogenase-deficiency.

Related Posts