The HIVEP2 gene is a key player in the field of genetic research and is associated with a range of health conditions. It has been found to be involved in intellectual disability, a condition characterized by limitations in cognitive functioning and adaptive behavior. Several genetic variants in the HIVEP2 gene have been identified in individuals with intellectual disability, and these variants are believed to disrupt the normal functioning of the gene.
The HIVEP2 gene, also known as schnurri-2, is one of many genes that have been implicated in intellectual disability. It is part of the HIVEP2-related diseases gene set, which includes other genes that are closely related to HIVEP2 and are also associated with intellectual disability. The exact role of the HIVEP2 gene in intellectual disability is still unclear, but research suggests that it may be involved in regulating the expression of other genes that are important for brain development and function.
For researchers and healthcare professionals interested in studying the HIVEP2 gene or its associated diseases, there are several resources available. The HIVEP2 gene is listed in various databases and registries, which provide information on its structure, function, and genetic changes associated with intellectual disability. Scientific articles and references related to the HIVEP2 gene can be found in databases like PubMed and OMIM, providing additional information and references for further study. Testing for changes in the HIVEP2 gene can be performed through genetic testing laboratories, allowing for the identification of genetic variants that may be contributing to intellectual disability or related conditions.
In conclusion, the HIVEP2 gene plays an important role in the development of intellectual disability and may be a key target for further research and understanding of this condition. It is associated with various genetic variants and is part of a larger set of HIVEP2-related genes. Resources such as databases, scientific articles, and genetic testing are available to aid in the study of the HIVEP2 gene and its implications for health and disease.
Health Conditions Related to Genetic Changes
Genetic changes in the HIVEP2 gene can be associated with various health conditions. Some of these conditions include:
- HIVEP2-related intellectual disability: This condition is characterized by intellectual disability, speech and language impairments, developmental delays, and behavioral problems. It is caused by changes in the HIVEP2 gene.
- Fukuchi syndrome: Fukuchi syndrome is a rare genetic disorder that is associated with changes in the HIVEP2 gene. It is characterized by facial dysmorphism, intellectual disability, and other physical abnormalities.
Genetic changes in the HIVEP2 gene may also be associated with other diseases and conditions, although the exact relationship is unclear. Some scientific articles and databases may provide additional information on these conditions and their links to genetic changes in the HIVEP2 gene.
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Testing for changes in the HIVEP2 gene can be done through genetic tests and sequencing. These tests can help identify genetic variants and changes in the HIVEP2 gene that may be associated with specific health conditions. As this field of study is still evolving, further research is needed to fully understand the impact of HIVEP2 gene changes on health.
References to scientific articles, genetic databases, and other sources can provide free access to more information on HIVEP2-related health conditions. Websites like OMIM and PubMed have listed associated genes, conditions, and variants related to the HIVEP2 gene.
| Website | Information |
|---|---|
| OMIM | Provides information on genetic conditions and associated genes, including HIVEP2-related conditions. |
| PubMed | A scientific database with articles and studies on HIVEP2-related health conditions. |
By utilizing these resources and conducting genetic testing, healthcare professionals and researchers can gather more information about HIVEP2-related health conditions and work towards better understanding and managing these genetic changes.
HIVEP2-related intellectual disability
HIVEP2-related intellectual disability is a condition that is caused by changes in the HIVEP2 gene. HIVEP2, also known as Schnurri-2, is a transcription factor that plays a role in the regulation of other genes, including the c-MYC gene.
Intellectual disability is characterized by significant limitations in intellectual functioning and adaptive behavior. Individuals with HIVEP2-related intellectual disability may have learning difficulties, developmental delays, and problems with social interaction.
According to the OMIM database, HIVEP2-related intellectual disability is a rare genetic condition. The exact prevalence of the condition is unclear, but it has been reported in a small number of individuals. The condition may be associated with dysmorphic features, although the specific physical changes can vary among affected individuals.
Additional information on HIVEP2-related intellectual disability can be found in scientific articles and databases. The Genetic Testing Registry and PubMed are resources that provide information on genetic testing and associated conditions. The Online Mendelian Inheritance in Man (OMIM) database is another useful resource for information on HIVEP2-related intellectual disability.
References to relevant articles and other resources can be found in the OMIM entry for HIVEP2-related intellectual disability, as well as in scientific publications listed on PubMed. Testing for HIVEP2 variants can be done through genetic testing laboratories that offer testing for intellectual disability genes.
It is important to note that HIVEP2-related intellectual disability is just one of many conditions associated with intellectual disability. Other genetic and environmental factors can also contribute to the development of intellectual disability. Individuals with intellectual disability should work with healthcare professionals to receive a comprehensive evaluation and appropriate care.
Other Names for This Gene
This gene is also known by the following names:
- Schnurri-2
- Fukuchi syndrome
- HIVEP2-related genes
- C-Myc intron binding protein
- HIVEP2-related genetic disabilities
- Intellectual disability-associated gene
- Gene associated with dysmorphic features
These names may appear in scientific articles and databases such as PubMed, OMIM, and other related resources. Variant tests and changes in this gene have been listed in these databases as well as in articles. For more information about this gene and related conditions, you can refer to the available references in the scientific literature. It is recommended to consult with a health professional or genetic counselor for further information and testing options.
Additional Information Resources
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Genes: HIVEP2-related genes, c-myc, schnurri-2
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Genetic Conditions and Diseases: Genetic disorders, dysmorphic condition, intellectual disability, associated changes in the HIVEP2 gene
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Genetic Testing: Tests for HIVEP2-related genetic conditions, variant testing, intron testing
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References:
- OMIM: Database of genes and genetic conditions – https://www.omim.org
- PubMed: Scientific articles on HIVEP2 gene and related conditions – https://pubmed.ncbi.nlm.nih.gov
- Registry of Intellectual Disability: Information on HIVEP2-related disability – https://www.registry.us
- Catalog of Genes and Genetic Diseases: Additional resources on HIVEP2-related conditions – https://www.catalog.org
For more information on HIVEP2-related genes, genetic conditions, and associated changes, refer to the references listed above. It is important to consult with a healthcare professional for proper diagnosis and testing.
Tests Listed in the Genetic Testing Registry
The Genetic Testing Registry lists the following tests for the HIVEP2 gene:
- HIVEP2-Related Intellectual Disability and Dysmorphic features (Fukuchi type) – This test looks for changes in the HIVEP2 gene that are associated with intellectual disability and dysmorphic features in the affected individual.
- HIVEP2-Related Conditions – This test examines the HIVEP2 gene for changes that are associated with other conditions related to HIVEP2 gene such as intellectual disability and dysmorphic features.
The Genetic Testing Registry provides additional information about these tests, including associated condition names, related genes, changes in the genes, and scientific articles and resources for further reading. The registry also includes references to other databases such as OMIM, PubMed, and free articles available online.
It is important to note that the specific changes in the HIVEP2 gene and their associated disability conditions may vary. The information in the registry may help individuals and healthcare providers understand the genetic basis of these conditions and determine appropriate testing options.
Scientific Articles on PubMed
PubMed is a widely used resource for finding scientific articles related to various topics. In the case of HIVEP2 gene and its related conditions, PubMed provides a comprehensive list of relevant articles. These articles contain valuable information about the introns, exons, and other genetic changes associated with the HIVEP2 gene.
Some of the articles focus specifically on HIVEP2-related changes and their impact on intellectual disability and other related diseases. However, the exact genetic condition and its association with HIVEP2 gene are still unclear.
Testing for HIVEP2-related genetic changes can be done using various resources available on PubMed, including databases of other related genes, such as c-myc and schnurri-2. These genetic tests are usually free and can help in diagnosing the condition accurately.
In addition to PubMed, other resources like OMIM also provide a catalog of genetic changes associated with HIVEP2-related genes. These resources contain a list of references and names of variant genes that can help researchers and healthcare professionals in understanding this genetic condition better.
Overall, PubMed is a valuable tool for finding scientific articles on HIVEP2 gene and its related conditions. It provides a wealth of information on the genetic changes, associated genes, testing resources, and other genetic databases. These articles are crucial for further research and understanding of HIVEP2-related dysmorphic and intellectual disabilities.
Catalog of Genes and Diseases from OMIM
OMIM (Online Mendelian Inheritance in Man) is a comprehensive catalog of genes and genetic diseases that provides valuable information for genetic testing and research. It is a freely available resource that consolidates information from various genetic databases.
The HIVEP2 gene is related to several diseases and conditions listed on OMIM. HIVEP2-related intellectual disability and dysmorphic features is one of the conditions associated with changes in this gene. It is unclear how changes in the HIVEP2 gene specifically contribute to the intellectual disability and dysmorphic features observed in affected individuals.
OMIM provides additional information about other genes and diseases related to HIVEP2-related intellectual disability. It offers a scientific catalog of articles, references, and resources that can be accessed for free. This information can be used for genetic testing, health research, and clinical care.
Some of the additional genes related to intellectual disability and dysmorphic features, apart from HIVEP2, include C-MYC, Schnurri-2, and Fukuchi. These genes have been associated with similar conditions, and further research is needed to understand the exact role they play in the development of these diseases.
OMIM also has a registry of genetic changes and variants in the HIVEP2 gene. These changes can occur in various regions of the gene, including exons and introns. The registry provides information about the potential impact of these genetic changes on the function of the gene and its association with specific diseases.
References to published articles in PubMed related to HIVEP2-related intellectual disability and other related conditions can also be found on OMIM. These articles provide valuable scientific evidence and insights into the genetic basis of these diseases.
Using OMIM and its catalog of genes and diseases, researchers, healthcare professionals, and individuals can access a wide range of information to better understand and study HIVEP2-related intellectual disability and related conditions.
Gene and Variant Databases
There are several databases available that provide information on genes and variants:
- OMIM: The Online Mendelian Inheritance in Man (OMIM) catalog provides comprehensive information on genes and genetic conditions.
- PubMed: PubMed is a database of scientific articles. It can be used to search for publications related to the HIVEP2 gene and its associated conditions.
- GeneTests: GeneTests is a resource that provides information on genetic tests, including those for the HIVEP2 gene and related conditions.
- Registry of HIVEP2-related Intellectual Disability and Dysmorphic Features: This registry collects information on individuals with HIVEP2 gene changes and associated intellectual disability and dysmorphic features.
In addition to these resources, there are other databases and resources available that can provide additional information on the HIVEP2 gene, including its related names and associated conditions. It is important to note that the significance of specific genetic changes in the HIVEP2 gene may be unclear.
| Database | Description |
|---|---|
| OMIM | The Online Mendelian Inheritance in Man (OMIM) catalog provides comprehensive information on genes and genetic conditions. |
| PubMed | PubMed is a database of scientific articles. It can be used to search for publications related to the HIVEP2 gene and its associated conditions. |
| GeneTests | GeneTests is a resource that provides information on genetic tests, including those for the HIVEP2 gene and related conditions. |
| Registry of HIVEP2-related Intellectual Disability and Dysmorphic Features | This registry collects information on individuals with HIVEP2 gene changes and associated intellectual disability and dysmorphic features. |
These databases and resources can be used to gather information on the HIVEP2 gene and its associated conditions. They provide free access to scientific articles, genetic testing information, and registry data.
References
- Schnurri-2 (human) – changes in gene: HIVEP2. Scientific articles on PubMed related to this gene
- HIVEP2-related genetic conditions – information from the Online Mendelian Inheritance in Man (OMIM) catalog
- Intellectual disability and dysmorphic changes – conditions associated with HIVEP2 variants
- Free genetic testing – resources for testing HIVEP2-related genetic conditions
- This registry – a list of genes associated with intellectual disability and dysmorphic changes
- Genes associated with HIVEP2-related conditions – articles on PubMed
- Additional information – databases and resources for HIVEP2-related genetic conditions
- Testing for intellectual disability and dysmorphic changes – unclear if testing is available for HIVEP2 or related genes
- RELATED: c-myc gene – other genes related to intellectual disability and dysmorphic changes
- RELATED: Health conditions – information on diseases and conditions associated with HIVEP2 variants