000NoneDISEASES is a frequently updated web resource that integrates evidence on disease-gene associations from automatic text mining, manually curated literature, cancer mutation data, and genome-wide association studies. We further unify the evidence by assigning confidence scores that facilitate comparison of the different types and sources of evidence. For further details please refer to the following Open Access preprint about the database: DISEASES: Text mining and data integration of disease-gene associations http://dx.doi.org/10.1101/008425 http://diseases.jensenlab.org/ 2014-09-03 20:28:00http://diseases.jensenlab.org/Entity?order=textmining,knowledge,experiments&textmining=10&knowledge=10&experiments=10&type1=9606&type2=-26&id1={{ensemblprotein}}2014-09-03 20:28:000.000.01167diseases.jensenlab.orgbiogpsusersIntegrating evidence on disease-gene associations from text mining, manually curated literature, cancer mutation data, and GWASpluginasu/profile/3/asuAndrew SupubliciframehumanDISEASES: Text mining and data integration of disease-gene associations000None2015-06-24 11:10:11{{refseqprotein}}2015-06-24 11:10:120.000.01186{{refseqprotein}}biogpsusersNo summary provided.pluginscm/profile/9200/scmscmpubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigprotein000None0.0networkhttp://giant.princeton.edu/contexts/integration/?id=202&gene={{entrezgene}}2015-09-10 21:27:260.002015-09-10 21:27:261193giant.princeton.edubiogpsusersGenome- scale Integrated Analysis of Networks in Tissuespluginben/profile/9358/benbenpubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigGIANT1015None2015-10-21 08:21:12http://www.scbt.com/display.php?category=Antibody&table=&search_catalog=2015-10-21 08:25:050.000.01198www.scbt.combiogpsusersSANTAplugina6523130/profile/9372/a6523130a6523130publiciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigSANTA000None0 googleliteraturescholarhttps://scholar.google.ca/scholar?hl=en&q={{symbol}}2016-02-21 23:11:34002016-02-21 23:11:341206scholar.google.cabiogpsuserspluginlilitmaria_/profile/9690/lilitmaria_Lilit Antonyanpubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigGoogle Scholar000None 2016-02-22 00:09:37http://www.mirbase.org/cgi-bin/query.pl?terms={{symbol}}2016-02-22 00:09:370001213www.mirbase.orgbiogpsuserspluginlilitmaria_/profile/9690/lilitmaria_Lilit Antonyanpubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigmiRNA000None0.0Search a Gene in a HGDP - CEPH Human Genome Diversity Genotype Database V3.0. Working example gene="THRAP3"genegeneticsmapmarkerssnphttp://www.cephb.fr/common/marker/markers.php?value_crit={{symbol}}&dbase_crit=gene_symbol&Submit=OK2016-03-23 14:51:220.002016-03-23 14:49:261218www.cephb.frbiogpsusersHGDP Genepluginyokofakun/profile/3118/yokofakunPierre LindenbaumpubliciframehumanCEPH000None0 Atlas allows searching for both validated and putative miRs binding genes of interest. May be searched by gene, miR, pathway, disease, and many more options.mirnahttp://zmf.umm.uni-heidelberg.de/apps/zmf/mirwalk2/2016-03-25 15:07:32002016-03-25 15:07:321220zmf.umm.uni-heidelberg.debiogpsusersAtlas for predicted and validated miRNA-target interactionspluginhkinkead/profile/4701/hkinkeadHeather Kinkeadpubliciframehumanmouseratzebrafishthale-cressmiRWalk 2.01015None0.0DIANA-TarBase is a manually curated catalogue of more than half a million published experimentally validated miRNA-gene interactions. It identifies both positive or negative experimental results, the utilized experimental methodology, experimental conditions including cell/tissue type and treatment. Searches can be done through gene or miRNA names.micrornamirnaregulationtargethttp://diana.imis.athena-innovation.gr/DianaTools/index.php?r=tarbase/index&genes={{symbol}}2016-05-04 15:01:170.002016-05-04 15:01:161225diana.imis.athena-innovation.grbiogpsusersmicroRNA-target interactions databaseplugineyleen.corrales/profile/9858/eyleen.corralesEyleen Corralespubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogDIANA-TarBase v7.0000None0.0MyGene2 is a portal through which families with rare genetic conditions who are interested in sharing their health and genetic information can connect with other families, clinicians, and researchers. The genetic cause of most rare conditions is unknown and as a result, most families who undergo exome sequencing or whole genome sequencing do not receive a diagnosis. By sharing information through MyGene2, a family can help and even participate in the discovery of new genetic conditions and the genes underlying these conditions. Families with rare genetic conditions may use MyGene2 to search for and contact other families who have the same condition or mutations in the same gene in order to share information and offer support. Families have the option to make the information they submit to MyGene2 available to anyone visiting the site (i.e., public) or available to only registered users who have also contributed data to MyGene2. Families also have the choice of whether or not they want to be contacted by clinicians and researchers or other families. Clinicians who have evaluated families with rare conditions may use MyGene2 to identify and contact families with the same rare condition and / or candidate gene. Researchers studying a gene or families with a rare condition may use MyGene2 to identify and contact other families who have the same rare condition or candidate gene.genegenetic-disordergeneticsvarianthttps://mygene2.org/MyGene2/variantsbygene?gene={{symbol}}2016-06-28 23:34:160.002016-06-28 23:34:041232mygene2.orgbiogpsusersMyGene2 is a portal through which families with rare genetic conditions can connect with other families, clinicians, and researchers.plugincwu/profile/2/cwuChunlei WupubliciframehumanMyGene2