Gene-, system- or disease-specific mutations
Online database for ALS genetic (SOD1, ALS2, VAPN and NEFH) mutations.
Search for published information on genes causing Alzheimer disease.
A web-portal for on-going collection, manual annotation and visualization of genes linked to autism.
Search for genetic mutations causing ALPS.
Find information about autophagy and self-digestion in eukaryotes.
Search for information on mutations of Bruton's agammaglobulinemia tyrosine kinase that causes XLA.
Find information about genes implicated in coronary artery disease.
Search for mutations causing defective CASR gene and related clinical information.
Search for published information on the genetics of epilepsy.
The Vitamin-K dependant serine protease mutation database.
Search for published data and information on human Cytokine gene polymorphism.
Search for information on genome-wide definitive haplotypes, determined using a collection of 74 Japanese complete hydatidiform moles (CHMs), each carrying a genome derived from a single sperm.
A resource for Eukaryotic DNA replication.
Find information on proteases and proteolysis.
A database of ethanol-related traits and behavioral responses to ethanol in humans and animal models.
A web resource for gene prioritization in multiple species.
To search for functions and homologous sequences of proteins that function in the eye.
Search for frequencies of causative mutations leading to inherited disorders worldwide.
Search for sequences of amyloid plaques forming peptides.
A neuroscience database aiming to present a global view of the role of synapse proteins in physiology and disease.
A web resource for prioritizing genes as candidates for inherited diseases.
Automatically provide large-scale lists of user-classified genes with functional profiles biologically characterizing the different gene classes in the list.
Search for biological pathway and genomic information of lipid-associated disorders.
Find comprehensive and integrated genetic information on human disease genes.
Search for information on genes related to human ageing and ageing process in different organisms.
Search detailed biological entries on oral microorganisms and the genes they express.
Search for known factor IX mutations due to small changes (base substitutions and short additions and/or deletions of <30 bp) identified in haemophilia B patients.
Search for information on the genomic sequence changes leading to hemoglobin variants and all types of thalassemia and hemoglobinopathies.
Search for information on human collagen mutations.
Search and analyze mutations at the human p53 and hprt genes and rodent transgenic lacI and lacZ genes
Search for information on mutations responsible for hereditary inflammatory disorders in human.
Type I, II and III IFN regulated genes manually curated from more than 28 publicly available microarray datasets.
Search for comprehensive information on Estrogen Responsive Genes.
Search for comprehensive information on Disease-causing protein kinase mutations.
Search for comprehensive information on OCRL1 mutations causing Lowe Syndrome.
Find information about genetic mutations associated with Parkinson's Disease.
Search for published and unpublished data and information on mutations and polymorphisms in the NCL genes.
Find information on human genes and genetic disorders.
Search the catalog of human genes and genetic disorders.
Search for curated information of nucleotide variation in the human PAH cDNA.
Search for genes or genomic loci related to the human prostate and prostatic diseases from this curated and integrated database.
Search for identified mutations in PHEX gene and related publications.
Search annotations for Pseudomonas aeruginosa genome.
A web-based compendium of molecular alterations in primary immunodeficiency diseases.
Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia.
Enables Type 1 diabetes researchers to analyze, store and share the complex data that biomedical researchers generate in the post-genomic era.
An integrated platform to study the molecular basis of Type 2 diabetes.
Search for comprehensive information about mutations of Androgen Receptor Gene.
Search for curated information on chromosome breakpoints and other genomic features related to autism.
Search for comprehensive annotated genomic information on human Chromosome 7.
Search for comprehensive information about Human PAX2 Allelic Variants.
Search for information on human PAX6 Allelic Variant.
Search for information of gene mutations causing the Lafora Progressive Myoclonus Epilepsy.
Provides up-to-date information about mutations of the TGFxdfR2 gene.
Search for information about diseases caused by miRNA deregulation.
Search for comprehensive information and knowledge on p53 genes.