Gene · 2014
Genotype-based databases for variants causing rare diseases.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Lanthaler Barbara, Wieser Stefanie, Deutschmann Andrea, Schossig Anna, Fauth Christine, Zschocke Johannes, Witsch-Baumgartner Martina
Аннотация
Inherited diseases are the result of DNA sequence changes. In recessive diseases, the clinical phenotype results from the combined functional effects of variants in both copies of the gene. In some diseases there is often considerable variability of clinical presentation or disease severity, which may be predicted by the genotype. Additional effects may be triggered by environmental factors, as well as genetic modifiers which could be nucleotide polymorphisms in related genes, e.g. maternal ApoE or ABCA1 genotypes which may have an influence on the phenotype of SLOS individuals. Here we report the establishment of genotype variation databases for various rare diseases which provide individual clinical phenotypes associated with genotypes and include data about possible genetic modifiers. These databases aim to be an easy public access to information on rare and private variants with clinical data, which will facilitate the interpretation of genetic variants. The created databases include ACAD8 (isobutyryl-CoA dehydrogenase deficiency (IBD)), ACADSB (short-chain acyl-CoA dehydrogenase (SCAD) deficiency), AUH (3-methylglutaconic aciduria (3-MGCA)), DHCR7 (Smith-Lemli-Opitz syndrome), HMGCS2 (3-hydroxy-3-methylglutaryl-CoA synthase 2 deficiency), HSD17B10 (17-beta-hydroxysteroid dehydrogenase X deficiency), FKBP14 (Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss; EDSKMH) and ROGDI (Kohlschütter-Tönz syndrome). These genes have been selected because of our specific research interests in these rare and metabolic diseases. The aim of the database was to include all identified individuals with variants in these specific genes. Identical genotypes are listed multiple times if they were found in several patients, phenotypic descriptions and biochemical data are included as detailed as possible in view also of validating the proposed pathogenicity of these genotypes. For DHCR7 genetic modifier data (maternal APOE and ABCA1 genotypes) is also included. Databases are available at http://databases.lovd.nl/shared/genes and will be updated based on periodic literature reviews and submitted reports.
Предметные рубрики MeSH
3-Hydroxyacyl CoA DehydrogenasesATP Binding Cassette Transporter 1Acyl-CoA DehydrogenaseAcyl-CoA DehydrogenasesAmelogenesis ImperfectaAmino Acid Metabolism, Inborn ErrorsApolipoproteins EDatabases, GeneticDementiaEhlers-Danlos SyndromeEnoyl-CoA HydrataseEpilepsyGenetic Association StudiesGenotypeHumansHydroxymethylglutaryl-CoA SynthaseHypoglycemiaInternetLipid Metabolism, Inborn ErrorsMembrane ProteinsMetabolism, Inborn ErrorsMitochondrial DiseasesMutationNuclear ProteinsOxidoreductases Acting on CH-CH Group DonorsPeptidylprolyl IsomerasePhenotypeRNA-Binding ProteinsRare DiseasesSmith-Lemli-Opitz Syndrome