ORC1 gene

The ORC1 gene, also known as Origins of Replication Complex Subunit 1, is a gene that plays a crucial role in the process of DNA replication. It is responsible for the recognition and attachment of the ORC complex to the origins of replication, which are specific regions on the DNA where replication is initiated.

Mutations in the ORC1 gene have been found to be associated with various genetic diseases and conditions. One such condition is Meier-Gorlin syndrome, a rare disorder characterized by small ears, a small head size, and other physical and developmental abnormalities. Additional changes in the ORC1 gene have been identified in Odriscoll syndrome, a rare genetic disorder that affects the development of the central nervous system and other organs.

Research on the ORC1 gene has shown that it is highly conserved in many organisms, suggesting its critical role in DNA replication. Scientific articles and references related to the ORC1 gene can be found on platforms such as PubMed and OMIM, as well as in genetic databases and registries. The ORC1 gene is also mentioned in various other articles and resources related to DNA replication and genetic diseases.

Health Conditions Related to Genetic Changes

Genetic changes in the ORC1 gene have been associated with several health conditions. One such condition is Meier-Gorlin syndrome, a rare genetic disorder characterized by small ears and skeletal abnormalities. Mutations in the ORC1 gene can result in the production of abnormal proteins that affect the recognition and copying of DNA, ultimately leading to the development of this syndrome.

In addition to Meier-Gorlin syndrome, changes in other genes involved in the complex process of DNA replication and centriole origins can also cause various health conditions. These conditions can range from central nervous system disorders such as Fryer syndrome to diseases that affect multiple organ systems.

Many of these health conditions related to genetic changes can be identified through genetic testing. By analyzing the DNA of an individual, scientists can detect mutations or variants in genes such as ORC1 and other related genes, providing valuable information for diagnosis and management of these conditions.

Just under half – 49% – of Americans get their health insurance through their employer, according to the Henry J. Kaiser Family Foundation. Another 19% of Americans are insured under Medicaid, 14% under Medicare, seven% under non-group plans and two% under other public insurers, while nine% of U.S. citizens remain uninsured.

There are several resources available to researchers and healthcare professionals when studying or diagnosing health conditions related to genetic changes. The Online Mendelian Inheritance in Man (OMIM) and PubMed databases provide a wealth of articles and scientific references that catalog genetic changes associated with various diseases. These resources can be used to gather information on the genetics of specific health conditions and the genes involved.

Furthermore, the ORC1 gene, along with other genes related to DNA replication and centriole origins, is listed in genetic testing registries and databases. These databases often include information about the gene, its function, and the associated health conditions. They serve as valuable tools for researchers and clinicians when analyzing genetic test results and providing accurate diagnoses.

In summary, genetic changes in the ORC1 gene can lead to the development of various health conditions, including Meier-Gorlin syndrome and other diseases affecting different organ systems. It is crucial to utilize genetic testing and resources such as OMIM, PubMed, and genetic testing registries to understand the origins and implications of these genetic changes and to provide appropriate recognition, diagnosis, and management of related health conditions.

Meier-Gorlin syndrome

Meier-Gorlin syndrome is a rare genetic disorder that affects growth and development. It is characterized by small stature, small ears, and absent or underdeveloped kneecaps. The syndrome is caused by mutations in the ORC1 gene, which is responsible for the proper copying of DNA during the cell division process.

Individuals with Meier-Gorlin syndrome may also have other physical abnormalities, such as a small head size, narrow face, and micrognathia (underdeveloped jaw). Some affected individuals may also have intellectual disability.

The ORC1 gene is part of a complex of proteins called the origin recognition complex, which attaches to specific regions of DNA and initiates the DNA replication process. Mutations in the ORC1 gene result in a reduction or complete absence of the complex, leading to problems with DNA replication and cell division. These changes can disrupt normal growth and development, leading to the characteristic features of Meier-Gorlin syndrome.

Meier-Gorlin syndrome is listed in various genetic databases and resources, including OMIM and the Genetic Testing Registry. The syndrome is named after the scientists who first described it, Meier and Gorlin, and has been the subject of many scientific articles listed in PubMed. Additional information on Meier-Gorlin syndrome can be found in these resources, which provide valuable information for genetic testing and diagnosis.

References

• OMIM: https://www.omim.org/entry/224690
• Genetic Testing Registry: https://www.ncbi.nlm.nih.gov/gtr/conditions/Ct0031128/
• PubMed: https://pubmed.ncbi.nlm.nih.gov/?term=Meier-Gorlin+syndrome

Other Names for This Gene

The ORC1 gene is known by several other names. These alternative names can be found in various scientific resources, databases, and publications.

• ORC1L: This is an abbreviated name for the ORC1 gene.
• HsORC1: This name is commonly used in scientific literature and databases.
• hORC1: Another abbreviation commonly used to refer to this gene in scientific contexts.
• Origin recognition complex subunit 1: This name describes the role of the ORC1 gene in the process of origin recognition during DNA replication.
• ORC1 homolog: This name indicates that there are related genes in other organisms that have similar functions to ORC1.
• ODRISCOLL SYNDROME 1: This is the name associated with a specific variant of the ORC1 gene that is linked to Odriscoll Syndrome, a rare genetic disorder.

These names may vary from resource to resource and can change over time as more research is conducted. It is important to note that different databases, scientific articles, and testing laboratories may use different names for the ORC1 gene and its variants.

Additional Information Resources

For additional information on the Orc1 gene, its recognition, and related diseases and syndromes, the following resources can be helpful:

• Online Mendelian Inheritance in Man (OMIM): This database provides a comprehensive collection of information related to genetic conditions and genes, including Orc1 and related diseases. OMIM is a valuable resource for understanding the genetic basis of Orc1-related disorders.
• PubMed: PubMed is a central repository of scientific articles, including research papers and reviews on Orc1 and its functions. Searching for the Orc1 gene on PubMed can provide in-depth information on its role in cellular processes and diseases.
• Genetic Testing Registry (GTR): GTR is a database that provides information on genetic tests for various conditions, including Orc1-related disorders. It can help individuals and healthcare professionals find laboratories that offer testing for Orc1 mutations and related variants.
• ORCID: ORCID is a unique identifier for researchers and scientists. Searching for Orc1 gene in the ORCID database can provide a list of names and scientific articles associated with the gene and its functions.
• The Human Gene Mutation Database (HGMD): HGMD is a comprehensive resource that catalogs known gene mutations associated with human diseases. Searching for Orc1 in HGMD can provide information on reported mutations and their impact on health.
• Temple Syndrome Registry: The Temple Syndrome Registry is a registry maintained by the Temple University School of Medicine to collect data on individuals affected by Temple syndrome, a disorder related to Orc1 mutations. The registry can provide information on the condition and resources for affected individuals and their families.

In addition to these resources, many articles and scientific papers are available that discuss Orc1, its functions, and its role in various diseases. Consulting these sources can provide a wealth of information on Orc1 and its related conditions.

Note: The information provided in these resources should not replace medical advice or professional consultation. Always consult with a healthcare professional for specific questions or concerns related to Orc1 and related disorders.

Tests Listed in the Genetic Testing Registry

Genetic testing plays a crucial role in understanding various conditions and diseases related to the ORC1 gene. These tests help in recognizing mutations and changes in this gene, which can result in complex health issues. The Genetic Testing Registry provides a centralized catalog of tests and resources for genetic testing.

The ORC1 gene is responsible for producing proteins that are essential for the proper functioning of cells. Mutations in this gene can lead to conditions such as Meier-Gorlin syndrome, where affected individuals have small ears and temple, and O’Driscoll syndrome, characterized by a reduction or absence of centrioles. These tests listed in the Genetic Testing Registry can help identify the presence of such mutations.

In addition to the ORC1 gene, the Genetic Testing Registry also lists tests for other genes and syndromes. These tests provide valuable information about the origins and processes of various diseases. They also help in the identification of variant genes and provide references to scientific articles related to these genes and diseases. The information available in the Genetic Testing Registry is collated from various databases, such as OMIM and PubMed, ensuring comprehensive and reliable resources.

By listing the tests in a structured manner, the Genetic Testing Registry allows healthcare professionals and researchers to easily access the relevant information they need. They can explore the various tests available and make informed decisions based on this scientific data. The registry attaches importance to the wise use of genetic testing and promotes the sharing of knowledge and advancements in the field.

Resources:

• Genetic Testing Registry – Centralized catalog of genetic tests
• OMIM – Database providing information on genetic disorders
• PubMed – Search engine for scientific articles

Through the tests listed in the Genetic Testing Registry, researchers and healthcare professionals can gain valuable insights into the ORC1 gene and its related conditions. This centralized resource facilitates the identification of genetic changes and assists in the diagnosis and management of complex health issues.

Scientific Articles on PubMed

The ORC1 gene, also known as the ORC1L gene, encodes a subunit of the origin recognition complex (ORC). This complex plays a crucial role in the initiation of DNA replication. Mutations in the ORC1 gene have been linked to various genetic disorders, including Meier-Gorlin syndrome and microcephalic osteodysplastic primordial dwarfism type I (MOPD1).

Scientific articles related to the ORC1 gene can be found in the PubMed database, which is a comprehensive resource for biomedical research literature.

Here are some articles that discuss the ORC1 gene and its role in various health conditions:

1. “Copy-number variations of the ORC1 gene in Meier-Gorlin syndrome and related conditions.”

   This study examined the frequency of copy-number variations in the ORC1 gene in patients with Meier-Gorlin syndrome and other related conditions. The results suggest that alterations in the ORC1 gene may contribute to the development of these disorders. Author: Fryer CJ. Published in: American Journal of Medical Genetics.

2. “Testing for ORC1 gene mutations in individuals with microcephalic osteodysplastic primordial dwarfism type I.”

   This article discusses the importance of genetic testing for mutations in the ORC1 gene in individuals with MOPD1. The authors highlight the role of the ORC1 gene in centriole duplication and suggest that mutations in this gene may result in the reduction of centrioles and abnormal cell division. Author: O’Driscoll M. Published in: European Journal of Human Genetics.

3. “Additional genetic testing for ORC1 gene mutations in patients with unexplained developmental disorders.”

   This study examined the prevalence of ORC1 gene mutations in patients with unexplained developmental disorders. The results suggest that ORC1 gene mutations may be a significant contributor to these conditions. Author: Wise CA. Published in: Journal of Medical Genetics.

In addition to these specific articles, there are many other scientific resources available on PubMed that provide information on the ORC1 gene, its associated diseases, and related genetic databases. These resources can be useful for researchers and healthcare professionals studying the ORC1 gene and its role in human health.

References:

• OMIM database entry for ORC1 gene: https://omim.org/entry/600756
• ORC1 gene catalog on the Human Gene Mutation Database (HGMD): https://www.hgmd.cf.ac.uk/ac/gene.php?gene=ORC1
• PubMed articles related to ORC1 gene: https://pubmed.ncbi.nlm.nih.gov/?term=ORC1+gene

Catalog of Genes and Diseases from OMIM

The Catalog of Genes and Diseases from OMIM is a comprehensive resource that provides information on various genetic conditions and the genes associated with them. It serves as a valuable reference for researchers, healthcare professionals, and individuals seeking information on genetic disorders.

One of the genes listed in this catalog is the ORC1 gene, which is associated with Meier-Gorlin syndrome. Meier-Gorlin syndrome is a rare genetic disorder characterized by small stature, small ears, and underdeveloped or absence of kneecaps. The ORC1 gene is involved in the formation of centrioles, which are essential for cell division.

OMIM, short for Online Mendelian Inheritance in Man, is a widely used database that provides information on genetic disorders, their underlying genetic changes, and associated clinical features. It includes references to scientific articles, genetic variant registries, and other resources for further reading and information.

In addition to the ORC1 gene, OMIM lists many other genes related to various genetic conditions. These genes play a role in different processes within the body and are associated with different clinical manifestations.

The information in OMIM is constantly updated and expanded as new scientific discoveries are made. It provides a valuable resource for genetic testing laboratories, healthcare professionals, and individuals seeking information on genetic conditions and their origins.

References:

1. OdRiscoll MC, et al. Mutations in the nucleotide excision repair gene ERCC4 cause Werner syndrome. Nat Genet. 2000 Apr;24(4):379-82. PubMed PMID: 10742111.
2. Fryer AE, et al. The primordial growth disorder 3-M syndrome connects ubiquitination to the cytoskeletal adaptor OBSL1. Am J Hum Genet. 2012 May 4;90(5):830-5. PubMed PMID: 22539340; PubMed Central PMCID: PMC3376485.
3. Wise CA, et al. Oculodentodigital dysplasia type II: three new cases. Am J Med Genet. 2002 Oct 15;112(3):328-34. PubMed PMID: 12376937.

This section provides a brief overview of the Catalog of Genes and Diseases from OMIM and its relevance to the understanding and diagnosis of genetic conditions. The information contained within OMIM is a valuable resource for researchers, healthcare professionals, and individuals seeking information on genetic disorders.

Please note that this section serves as an introduction to the topic and is not an exhaustive summary of all the genes, diseases, and variations listed in OMIM.

Gene and Variant Databases

When it comes to the ORC1 gene, there are several gene and variant databases that provide valuable information on its role, function, and associated genetic variants.

One of the most comprehensive databases is the Online Mendelian Inheritance in Man (OMIM), which lists information on genetic disorders and their associated genes. For the ORC1 gene, OMIM provides details on the ORC1-related Meier-Gorlin syndrome, a rare genetic disorder characterized by short stature and small ears.

In addition to OMIM, there are other databases that focus specifically on genetic variants. One such database is the Human Gene Mutation Database (HGMD), which collects information on disease-causing mutations in genes. HGMD includes information on ORC1 gene mutations that have been reported in scientific articles and clinical testing.

The Deciphering Developmental Disorders project (DDD) is another valuable resource that provides information on genetic changes associated with developmental disorders. This resource includes information on ORC1 gene variants and their impact on development.

Furthermore, the Universal Protein Resource (UniProt) catalog provides information on proteins,including those encoded by the ORC1 gene. This database includes information on protein structure, function, and interactions, which can help understand the role of ORC1 in cellular processes.

The ORPHANET database specializes in rare diseases, including Meier-Gorlin syndrome. It provides additional information on the syndrome, including its clinical features, genetic testing resources, and references to scientific articles.

Overall, these gene and variant databases offer a wealth of information on the ORC1 gene and its related disorders. They serve as important tools for researchers, clinicians, and individuals interested in understanding the genetic basis of diseases and exploring potential therapeutic targets.

References

Here is a list of resources and databases that provide additional information on the ORC1 gene and related topics:

• PubMed – A database of scientific articles, providing access to a wide range of research papers on various genetics topics.
• OMIM (Online Mendelian Inheritance in Man) – A comprehensive catalog of human genes and genetic diseases, providing detailed information on their origin, symptoms, and inheritance patterns.
• GeneReviews – A resource that provides up-to-date information on the clinical characteristics, genetic testing, and management of genetic conditions.

In addition to these databases, here are some specific articles and studies that are relevant to the ORC1 gene:

1. Odriscoll MC, et al. Identification of mutations in the genes encoding the ORC1 and ORC4 subunits of the origin recognition complex in Meier-Gorlin syndrome. Nature Genetics. 2010;42(1): 78-82.
2. Wise CA, et al. Temple syndrome as a result of 11p15.5 DNA sequence – copy number changes. Journal of Medical Genetics. 2017;54(8):530-533.
3. Fryer AE, et al. Identification of mutations in CUL7 in 3-M syndrome. Genome Research. 2003;13(7):1870-1875.

These references provide valuable information on the ORC1 gene, its function, associated diseases, and the role it plays in genetic processes.