000human58.0Alternative Splicing Gallery (ASG) is a web-based splicing graph database that integrates transcript information from Ensembl, RefSeq, STACK, TIGR gene index, and UniGene, in order to explore and visualize gene structure and alternative splicing and to provide an exhaustive transcript catalog. The program was developed by Jeremy Leipzig and Dr. Steffen Heber.exonexpressiongeneticssplicinghttp://statgen.ncsu.edu/asg/index.php?lookupType=match&lookupValue={{EnsemblGene}}2011-05-03 22:46:2758.0512008-11-25 12:04:30221statgen.ncsu.edubiogpsusersAlternative Splicing Gallery (ASG) is a web-based splicing graph database that integrates transcript information from Ensembl, RefSeq,...pluginkrzysztof/profile/123/krzysztofChris WypijewskipubliciframehumanAlternative Splicing Gallery000True58.0Search by gene symbol at Google Scholar.genegoogleliteraturescholarsymbolhttp://scholar.google.com/scholar?q={{symbol}}2013-08-14 17:39:2658.0442008-05-06 03:20:4549scholar.google.combiogpsusersSearch by gene symbol at Google Scholar.pluginasu/profile/3/asuAndrew Supubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigGoogle Scholar search (gene symbol)000None55.0Display ingenuity gene report (requires login). Pathway information.pathwayhttps://analysis.ingenuity.com/pa/api/v2/geneview?geneid={{EntrezGene}}&geneidtype=entrezgene&applicationname=BioGPS2010-05-04 00:10:1155.0392008-04-16 19:13:0215analysis.ingenuity.combiogpsusersDisplay ingenuity gene report (requires login). Pathway information.pluginasu/profile/3/asuAndrew Supubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigIngenuity000None54.0A network of concurring genes and proteins extends through the scientific literature touching on phenotypes, pathologies and gene function. iHOP provides this network as a natural way of accessing millions of PubMed abstracts. By using genes and proteins as hyperlinks between sentences and abstracts, the information in PubMed can be converted into one navigable resource, bringing all advantages of the internet to scientific literature research.literaturenetworkpubmedhttp://www.ihop-net.org/UniPub/iHOP/in?dbrefs_1=NCBI_GENE__ID|{{EntrezGene}}2009-02-03 00:02:5454.0442009-02-03 00:02:54322www.ihop-net.orgbiogpsusersA network of concurring genes and proteins extends through the scientific literature touching on phenotypes, pathologies and gene...pluginasu/profile/3/asuAndrew Supubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigiHOP - Information Hyperlinked over Proteins 000None54.0 The Pfam database is a large collection of protein families, each represented by multiple sequence alignments and hidden Markov models (HMMs). Proteins are generally composed of one or more functional regions, commonly termed domains. Different combinations of domains give rise to the diverse range of proteins found in nature. The identification of domains that occur within proteins can therefore provide insights into their function. There are two components to Pfam: Pfam-A and Pfam-B. Pfam-A entries are high quality, manually curated families. Although these Pfam-A entries cover a large proportion of the sequences in the underlying sequence database, in order to give a more comprehensive coverage of known proteins we also generate a supplement using the ADDA database. These automatically generated entries are called Pfam-B. Although of lower quality, Pfam-B families can be useful for identifying functionally conserved regions when no Pfam-A entries are found. Pfam also generates higher-level groupings of related families, known as clans. A clan is a collection of Pfam-A entries which are related by similarity of sequence, structure or profile-HMM. familieshomologyproteinhttp://pfam.sanger.ac.uk/protein/{{Uniprot}}2009-09-10 01:11:4554.0422009-05-01 00:03:18428pfam.sanger.ac.ukbiogpsusers The Pfam database is a large collection of protein families, each represented by multiple sequence alignments and hidden Markov models...pluginivaagenes/profile/877/ivaagenesIan Vaagenespubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigPFAM000human52.0HuGE Navigator provides access to a continuously updated knowledge base in human genome epidemiology, including information on population prevalence of genetic variants, gene-disease associations, gene-gene and gene- environment interactions, and evaluation of genetic tests.geneticshttp://hugenavigator.net/HuGENavigator/huGEPedia.do?firstQuery=none&typeSubmit=GO&check=y&typeOption=gene&which=2&pubOrderType=pubD&geneID={{EntrezGene}}2011-05-03 22:47:2052.0432008-07-03 19:29:1880hugenavigator.netbiogpsusersHuGE Navigator provides access to a continuously updated knowledge base in human genome epidemiology, including information on population...pluginasu/profile/3/asuAndrew SupubliciframehumanHuGE Navigator000True50.0STITCH is a resource to explore known and predicted interactions of chemicals and proteins. Chemicals are linked to other chemicals and proteins by evidence derived from experiments, databases and the literature. STITCH contains interactions for over 68,000 chemicals and over 1.5 million proteins in 373 species. http://www.ncbi.nlm.nih.gov/pubmed/18084021proteinhttp://stitch.embl.de/interactions/{{EnsemblGene}}2010-06-09 16:56:4250.0412008-11-02 03:27:19179stitch.embl.debiogpsusersSTITCH is a resource to explore known and predicted interactions of chemicals and proteins. Chemicals are linked to other chemicals and...pluginbiocs/profile/3209/biocsMichael Kuhnpubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigSTITCH: Chemical-Protein Interactions000human49.0All cancers arise as a result of the acquisition of a series of fixed DNA sequence abnormalities, mutations, many of which ultimately confer a growth advantage upon the cells in which they have occurred. There is a vast amount of information available in the published scientific literature about these changes. COSMIC is designed to store and display somatic mutation information and related details and contains information relating to human cancers.cancergeneticsmutationsnphttp://cancer.sanger.ac.uk/cosmic/gene/analysis?ln={{symbol}}2016-03-16 16:51:3149.0412008-12-23 00:16:04263cancer.sanger.ac.ukbiogpsusersAll cancers arise as a result of the acquisition of a series of fixed DNA sequence abnormalities, mutations, many of which ultimately...pluginasu/profile/3/asuAndrew SupubliciframehumanCOSMIC -- Catalogue Of Somatic Mutations In Cancer000None49.0IntAct provides a freely available, open source database system and analysis tools for protein interaction data. All interactions are derived from literature curation or direct user submissions and are freely available.proteinhttp://www.ebi.ac.uk/intact/binary-search/faces/search.xhtml?query={{Symbol}}2009-05-05 00:02:3249.0312009-05-01 16:23:31431www.ebi.ac.ukbiogpsusersIntAct provides a freely available, open source database system and analysis tools for protein interaction data. All interactions are...pluginivaagenes/profile/877/ivaagenesIan Vaagenespubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigIntAct613None48.0ArrayExpress is a public repository for microarray based gene expression data.expressionhttp://www.ebi.ac.uk/microarray-as/atlas/gene?gid={{EnsemblGene}}2009-05-05 00:02:3248.0412009-05-01 15:39:34430www.ebi.ac.ukbiogpsusersArrayExpress is a public repository for microarray based gene expression data.pluginivaagenes/profile/877/ivaagenesIan Vaagenespubliciframehumanmouseratfruitflynematodezebrafishthale-cressfrogpigArrayExpress