000None0.0Search 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 WupubliciframehumanMyGene2000None 2017-05-24 19:42:04ciliac2017-05-24 19:42:040001249ciliacbiogpsuserspluginmotaz/profile/10603/motazmotazpubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigCYCS000None 2017-12-14 23:31:04http://www.ncbi.nlm.nih.gov/pubmed/?term=Albumin+AND+{{Symbol}}2017-12-14 23:31:040001256www.ncbi.nlm.nih.govbiogpsuserspluginchrau/profile/5666/chrauchraupubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigAlbumin Pubmed000None 2018-05-22 08:40:01https://japantobacco.ussc.informatics.illumina.com/c/nextbio.nb2018-05-22 08:40:010001268japantobacco.ussc.informatics.illumina.combiogpsuserspluginShiraki/profile/11131/ShirakiShirakipubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigBaseSpace000None0RNA sequencing (RNA-seq) is the leading technology for genome-wide transcript quantification. However, publicly available RNA-seq data is currently provided mostly in raw form, a significant barrier for global and integrative retrospective analyses. ARCHS4 is a web resource that makes the majority of published RNA-seq data from human and mouse available at the gene and transcript levels. For developing ARCHS4, available FASTQ files from RNA-seq experiments from the Gene Expression Omnibus (GEO) were aligned using a cloud-based infrastructure. In total 187,946 samples are accessible through ARCHS4 with 103,083 mouse and 84,863 human. Additionally, the ARCHS4 web interface provides intuitive exploration of the processed data through querying tools, interactive visualization, and gene pages that provide average expression across cell lines and tissues, top co-expressed genes for each gene, and predicted biological functions and protein-protein interactions for each gene based on prior knowledge combined with co-expression. See https://www.ncbi.nlm.nih.gov/pubmed/29636450rna-seqhttps://amp.pharm.mssm.edu/archs4/gene/{{symbol}}2018-06-18 15:01:13002018-06-18 15:01:131270amp.pharm.mssm.edubiogpsusersARCHS4 is a web resource that makes the majority of published RNA-seq data from human and mouse available at the gene and transcript levelsplugingtsueng/profile/7731/gtsuenggtsuengpubliciframehumanmouseARCHS4000None 2018-10-09 01:26:05http://lifeome.net/database/hccdb/search.html2018-10-09 01:26:050001275lifeome.netbiogpsuserspluginMZCS/profile/11065/MZCSMZCSpubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpiglifeome000None 2021-06-19 22:59:27https://www.wikigenes.org/e/gene/e/{{EntrezGene}}.html2021-06-19 22:59:270001282www.wikigenes.orgbiogpsuserspluginvictor_trevino/profile/2323/victor_trevinoVictor Trevinopubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigWikiGenes