Orthodisease

Names

More detailed information about this field from each metasource. ×

Orthodisease

metasource: bio.tools
version: extracted_at: 2022-11-04T11:35:30.239686

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orthodisease

metasource: bio.tools
version: extracted_at: 2022-11-04T11:35:30.239686

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database of Disease-Gene Associations with annotated Relationships

The database of Disease-Gene Associations with annotated Relationships (eDGAR) is a database for collecting and organizing the data on gene/disease associations as derived from OMIM, Humsavar and Clin ...

Networks of Functional Coupling of proteins

FunCoup is a framework to infer genome-wide functional couplings in 11 model organisms. Functional coupling, or functional association, is an unspecific form of association that encompasses direct phy ...

siRNAdb

The siRNA database provides a gene-centric view of human siRNA experimental data, including siRNAs of known efficacy and siRNAs predicted to be of high efficacy by siSearch. Linked to these sequences ...

Stockholm Multiple Alignment Format

The "Stockholm" format is a system for marking up features in a multiple alignment. These mark-up annotations are preceded by a 'magic' label, of which there are four types. The Stockholm format is us ...

HieranoiDB

Ortholog groups and trees for 66 proteomes inferred by Hieranoid 2

Collagen Mutation Database (CMD)

Database of osteogenesis imperfecta and type III collagen variants.

MTCards

A database of mitochondrial genome variants in chinese population

KinMutBase

KinMutBase is a comprehensive database of disease-causing mutations in protein kinase domains. This resources provides plenty of information, namely mutation statistics and display, clickable sequence ...

RHIVDB

Database of HIV Amino Acid Sequences and Clinical Data of Infected Patients.

TissueNexus

A database of human tissue functional gene networks built with a large compendium of curated RNA-seq data.

Evolutionary Annotation Database

Evola contains ortholog information of all human genes among vertebrates. Orthologs are a pair of genes in different species that evolved from a common ancestral gene by speciation. In Evola, ortholog ...

Domain mapping of disease mutations

Domain mapping of disease mutations (DMDM) is a database in which each disease mutation can be displayed by its gene, protein or domain location.

MalaCards

The MalaCards human disease database (http://www. malacards.org/) is an integrated compendium of annotated diseases mined from 68 data sources. MalaCards has a web card for each of ∼20 000 disease ent ...

Santa Barbara Coastal Observation Ontology

Extensible Observation Ontology for the Santa Barbara Coastal Long Term Ecological Research project (SBC-LTER). OBOE SBC extends core concepts defined in the OBOE suite that are particular to the San ...

BrainEXP-NPD

Database of transcriptomic profiles of human brains of six neuropsychiatric disorders.

dbCoRC

PhosSNP

A database of phosphorylation-related SNP (phosSNP) which are non-synonymous SNP (nsSNP) that affect the protein phosphorylation status. Using an in-house developed kinase-specific phosphorylation sit ...

DISNOR

DISNOR is a resource that uses a comprehensive collection of disease associated genes, as annotated in DisGeNET, to interrogate SIGNOR (https://signor.uniroma2.it) in order to assemble disease-specifi ...

GenomeTraFaC

GenomeTraFaC is a database of conserved regulatory elements obtained by systematically analyzing the orthologous set of human and mouse genes. It mainly focuses on all of the high-quality mRNA entries ...