Other names: gene4hl
An Integrated Genetic Database for Hearing Loss.
genotype and phenotype sequencing genetic engineering genetic variation gene expression
A genetic resource database for rubber tree genomic study | Molecular & Genetic Resources for Hevea tree
an integrated database and analytic platform for de novo mutations in humans. De novo mutations (DNMs) significantly contribute to sporadic diseases, particularly in neuropsychiatric disorders. Whole ...
Genotype-Tissue Expression (GTEx) - database which helps to study the relationship between genetic variation and gene expression in human tissues.
GPCards is an integrated database of genotype-phenotype correlations in human genetic diseases.
AOE (All Of gene Expression) - an integrated index for public gene expression databases.
GEnetic Antibiotic Resistance and Susceptibility Database.
A generic integrated web-based workflow system to evaluate genotype-phenotype correlations in human mitochondrial diseases.
An integrated omics database for functional genomic analysis of cyanobacteria.
Computational tools and libraries for CRISPR/Cas9-derived RNA-guided engineered nucleases (RGENs).
The Human Genetic Variation Database (HGVD) aims to provide a central resource to archive and display Japanese genetic variation and association between the variation and transcription level of genes. ...
a comprehensive genetic database of Parkinson's disease. Gene4PD: an integrative genomic database and analytic platform for Parkinson's disease. Rare variants identified from PD patients.
PhenoModifier is a genetic modifier database for elucidating the genetic basis of human phenotypic variation. PhenoModifier provides a more complete spectrum of genetic factors contributing to human p ...
CanVaS is a Greek cancer patient genetic variation resource.
BEable-GPS: Base Editable prediction of Global Pathogenic-related SNVs. Comparison of cytosine base editors and development of the BEable-GPS database for targeting pathogenic SNVs.
MGI is the international database resource for the laboratory mouse, providing integrated genetic, genomic, and biological data to facilitate the study of human health and disease.
dbMTS is a comprehensive database of putative human microRNA target site (MTS) SNVs and their functional predictions. dbMTS collects all potential SNVs microRNA target seed regions in human 3’UTRs and ...
PharmGKB is a resource that provides information about how human genetic variation affects response to medications. PharmGKB collects, curates and disseminates knowledge about clinically actionable ge ...
Genetic mutation database for rare diseases that enables to search, sort and filter genetic variants from clinically diagnosed individuals worldwide and make symptoms-based queries.
An Evidence-based Database of Genes and Phenotypes of Male Infertility.
A genetic database for attention deficit hyperactivity disorder. ADHDgene aims to provide research community with a central genetic resource and analysis platform for ADHD, to help unveil the genetic ...