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Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Specification URL Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
Arabidopsis Reactome
 
Resource Report
Resource Website
1+ mentions
Arabidopsis Reactome (RRID:SCR_002063) data or information resource, database Curated database of core pathways and reactions in plant biology that covers biological pathways ranging from the basic processes of metabolism to high-level processes such as cell cycle regulation. While it is targeted at Arabidopsis pathways, it also includes many biological events from other plant species. This makes the database relevant to the large number of researchers who work on other plants. Arabidopsis Reactome currently contains both in-house curated pathways as well as imported pathways from AraCyc and KEGG databases. All the curated information is backed up by its provenance: either a literature citation or an electronic inference based on sequence similarity. Their ontology ensures that the various events are linked in an appropriate spatial and temporal context. pathway, reaction, biological process uses: AraCyc
uses: KEGG
is listed by: 3DVC
has parent organization: John Innes Centre; Norwich; United Kingdom
European Union LSHG-CT-2006-037704 THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-20812 SCR_002063 Arabidopsis Reactome - a curated knowledgebase of plant biological pathways 2026-08-29 11:29:12 3
ConsensusPathDB
 
Resource Report
Resource Website
500+ mentions
ConsensusPathDB (RRID:SCR_002231) CPDB data or information resource, database An integrative interaction database that integrates different types of functional interactions from heterogeneous interaction data resources. Physical protein interactions, metabolic and signaling reactions and gene regulatory interactions are integrated in a seamless functional association network that simultaneously describes multiple functional aspects of genes, proteins, complexes, metabolites, etc. With human, yeast and mouse complex functional interactions, it currently constitutes the most comprehensive publicly available interaction repository for these species. Different ways of utilizing these integrated interaction data, in particular with tools for visualization, analysis and interpretation of high-throughput expression data in the light of functional interactions and biological pathways is offered. gene regulatory network, pathway, gene regulatory network, molecular interaction, interaction, gene regulation, protein interaction, genetic interaction, biochemical reaction, drug-target interaction, molecule, visualization, gene, protein, complex, metabolite, FASEB list is listed by: OMICtools
is related to: BIND
is related to: BioCarta Pathways
is related to: Biological General Repository for Interaction Datasets (BioGRID)
is related to: CORUM
is related to: Database of Interacting Proteins (DIP)
is related to: DrugBank
is related to: HPRD - Human Protein Reference Database
is related to: HumanCyc: Encyclopedia of Homo sapiens Genes and Metabolism
is related to: Integrating Network Objects with Hierarchies
is related to: InnateDB
is related to: IntAct
is related to: KEGG
is related to: MINT
is related to: MIPS Mammalian Protein-Protein Interaction Database
is related to: MatrixDB
is related to: NetPath
is related to: Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB)
is related to: PDZBase
is related to: Pathway Interaction Database
is related to: PIG - Pathogen Interaction Gateway
is related to: PINdb
is related to: PharmGKB
is related to: PhosphoPOINT
is related to: PhosphoSitePlus: Protein Modification Site
is related to: Reactome
is related to: Small Molecule Pathway Database
is related to: SignaLink
is related to: SPIKE
is related to: Therapeutic Target Database
is related to: WikiPathways
has parent organization: Max Planck Institute for Molecular Genetics; Berlin; Germany
European Union HEALTH-F4-2007-200767 PMID:23143270
PMID:21071422
PMID:20847220
PMID:18940869
Free, Freely available nif-0000-02684, OMICS_01903, r3d100012822 https://doi.org/10.17616/R3HF8Z SCR_002231 ConsensusPathDB, ConsensusPathDB-human 2026-08-29 11:29:16 722
EPILEPSIE database
 
Resource Report
Resource Website
1+ mentions
EPILEPSIE database (RRID:SCR_003179) data or information resource, database A comprehensive database for human surface and intracranial EEG data that is suitable for a broad range of applications e.g. of time series analyses of brain activity. Currently, the EU database contains annotated EEG datasets from more than 200 patients with epilepsy, 50 of them with intracranial recordings with up to 122 channels. Each dataset provides EEG data for a continuous recording time of at least 96 hours (4 days) at a sample rate of up to 2500 Hz. Clinical patient information and MR imaging data supplement the EEG data. The total duration of EEG recordings included execeeds 30000 hours. The database is composed of different modalities: Binary files with EEG recording / MR imaging data and Relational database for supplementary meta data. seizure, electroencephalography, mri, eeg recording, metadata, intracranial, surface, time series analyses, brain activity, brain, clinical, image collection is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
has parent organization: University of Freiburg; Baden-Wurttemberg; Germany
Epilepsy Excellence Initiative of the German Federal and State Governments ;
European Union 211713;
BMBF 01GQ0420;
German Science Foundation Ti 315/4-2
PMID:22738131 Free, Freely available nlx_156892 http://www.nitrc.org/projects/epilepsiaedb http://epilepsy-database.eu/project/ http://www.epilepsiae.eu http://epilepsy-database.eu SCR_003179 EPILEPSIAE Project Database, European Epilepsy Database 2026-08-29 11:29:21 3
FIVA - Functional Information Viewer and Analyzer
 
Resource Report
Resource Website
1+ mentions
FIVA - Functional Information Viewer and Analyzer (RRID:SCR_005776) FIVA data processing software, software application, software resource Functional Information Viewer and Analyzer (FIVA) aids researchers in the prokaryotic community to quickly identify relevant biological processes following transcriptome analysis. Our software is able to assist in functional profiling of large sets of genes and generates a comprehensive overview of affected biological processes. Currently, seven different modules containing functional information have been implemented: (i) gene regulatory interactions, (ii) cluster of orthologous groups (COG) of proteins, (iii) gene ontologies (GO), (iv) metabolic pathways (v) Swiss Prot keywords, (vi) InterPro domains - and (vii) generic functional categories. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible gene, gene expression, gene expression pattern, functional profile, statistical analysis, metabolic pathway, gene ontology, function, ortholog, gene regulatory interaction, biological process, transcriptome, visualization, analysis is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: MolGen
Netherlands Organization for Scientific Research ;
industrial partners in the NWO-BMI project number 050.50.206 on Computational Genomics of Prokaryotes ;
Center IOP Genomics ;
European Union QLK3-CT-2001-01473
PMID:17237043 Free for academic use nlx_149245 SCR_005776 FIVA - Functional Information Viewer Analyzer, Functional Information Viewer and Analyzer (FIVA), Functional Information Viewer and Analyzer 2026-08-29 11:28:42 1
Orphanet
 
Resource Report
Resource Website
100+ mentions
Orphanet (RRID:SCR_006628) Orphanet data or information resource, portal European website providing information about orphan drugs and rare diseases. It contains content both for physicians and for patients. Reference portal for rare diseases and orphan drugs to help improve diagnosis, care and treatment of patients with rare diseases. drug, clinical, diagnostic, test, rare, disease, molecule, gene, orphan, drug is used by: NIF Data Federation
is used by: HmtPhenome
is listed by: OMICtools
is related to: Disease core ontology applied to Rare Diseases
is related to: phenomeNET
has parent organization: National Institute of Health and Medical Research; Rennes; France
is parent organization of: Orphanet Rare Disease Ontology
European Union ;
French Directorate General for Health ;
National Institute of Health and Medical Research ;
Rennes ;
France
Free, Freely available nif-0000-21306, grid.458406.b, Wikidata: Q1515833 https://ror.org/03d3kf570 SCR_006628 2026-08-29 11:28:44 474
Julearn
 
Resource Report
Resource Website
1+ mentions
Julearn (RRID:SCR_024881) software library, software resource, software toolkit Software library of easy testing ML models directly from pandas DataFrames, while keeping the flexibility of using scikit-learn’s models. machine learning open source, leakage free evaluation, inspection of ML models, testing ML models, Deutsche Forschungsgemeinschaft PA 3634/1-1;
Deutsche Forschungsgemeinschaft 431549029–SFB 1451 project B05;
European Union HORIZON-INFRA-2021-TECH-01;
Helmholtz-AI ZT-I-PF-5-078;
Helmholtz Supercomputing and Modeling for the Human Brain;
Helmoltz Imaging Platform NimRLS
DOI:10.48550/arXiv.2310.12568. Free, Available for download, Freely available https://github.com/juaml/julearn SCR_024881 2026-08-29 11:33:46 7
Sanger Mouse Resources Portal
 
Resource Report
Resource Website
50+ mentions
Sanger Mouse Resources Portal (RRID:SCR_006239) Sanger Mouse Portal, WTSI Mouse Resources Portal, WTSI Mouse Resource Portal biomaterial supply resource, material resource Database of mouse research resources at Sanger: BACs, targeting vectors, targeted ES cells, mutant mouse lines, and phenotypic data generated from the Institute''''s primary screen. The Wellcome Trust Sanger Institute generates, characterizes, and uses a variety of reagents for mouse genetics research. It also aims to facilitate the distribution of these resources to the external scientific community. Here, you will find unified access to the different resources available from the Institute or its collaborators. The resources include: 129S7 and C57BL6/J bacterial artificial chromosomes (BACs), MICER gene targeting vectors, knock-out first conditional-ready gene targeting vectors, embryonic stem (ES) cells with gene targeted mutations or with retroviral gene trap insertions, mutant mouse lines, and phenotypic data generated from the Institute''''s primary screen. bacterial artificial chromosome, vector, embryonic stem cell, mutant mouse line, phenotype, gene, knockout, gene expression, genetics, chromosome, mutant, mouse line, mammal, marker symbol is listed by: One Mind Biospecimen Bank Listing
is related to: Ensembl
has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom
Wellcome Trust 079643;
Wellcome Trust 098051;
NHGRI UO1-HG004080;
NCRR 1-U42RR033192;
European Union LSHG-CT-2006-037188;
European Union 227490;
European Union 312325;
European Union 261492
For the scientific community nlx_151819 SCR_006239 Mouse Resources Portal, Wellcome Trust Sanger Institute Mouse Resources Portal 2026-08-29 11:30:48 52
ProteomeXchange
 
Resource Report
Resource Website
5000+ mentions
ProteomeXchange (RRID:SCR_004055) catalog, consortium, data or information resource, data repository, database, organization portal, portal, service resource, storage service resource A data repository for proteomic data sets. The ProteomeExchange consortium, as a whole, aims to provide a coordinated submission of MS proteomics data to the main existing proteomics repositories, as well as to encourage optimal data dissemination. ProteomeXchange provides access to a number of public databases, and users can access and submit data sets to the consortium's PRIDE database and PASSEL/PeptideAtlas. consortium, database, proteomics, MS proteomics, protein, mass spectrometry, bio.tools, FASEB list uses: Proteomics Identifications (PRIDE)
uses: PeptideAtlas
is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: bio.tools
is listed by: Debian
is affiliated with: Omics Discovery Index
is related to: Proteomics Identifications (PRIDE)
is related to: PeptideAtlas
is related to: SIB Swiss Institute of Bioinformatics
is related to: Mass spectrometry Interactive Virtual Environment (MassIVE)
is related to: European Bioinformatics Institute
is related to: ProteomeTools
is related to: Integrated Proteome Resources
has parent organization: European Bioinformatics Institute
European Union 260558 Public, The community can contribute to this resource r3d100012122, nlx_158620, biotools:proteomexchange http://proteomecentral.proteomexchange.org, https://bio.tools/proteomexchange, https://doi.org/10.17616/R32D29 SCR_004055 , ProteomeXchange, Proteome Exchange 2026-08-29 11:27:43 6107
Pathbase
 
Resource Report
Resource Website
10+ mentions
Pathbase (RRID:SCR_006141) Pathbase controlled vocabulary, data access protocol, data or information resource, data repository, database, image collection, image repository, ontology, service resource, software resource, storage service resource, web service Database of histopathology photomicrographs and macroscopic images derived from mutant or genetically manipulated mice. The database currently holds more than 1000 images of lesions from mutant mice and their inbred backgrounds and further images are being added continuously. Images can be retrieved by searching for specific lesions or class of lesion, by genetic locus, or by a wide set of parameters shown on the Advanced Search Interface. Its two key aims are: * To provide a searchable database of histopathology images derived from experimental manipulation of the mouse genome or experiments conducted on genetically manipulated mice. * A reference / didactic resource covering all aspects of mouse pathology Lesions are described according to the Pathbase pathology ontology developed by the Pathbase European Consortium, and are available at the site or on the Gene Ontology Consortium site - OBO. As this is a community resource, they encourage everyone to upload their own images, contribute comments to images and send them their feedback. Please feel free to use any of the SOAP/WSDL web services. (under development) histopathology, photomicrograph, macroscopic, mutant, genetically manipulated, pathology, transgenic, rodent, mpath ontology, mouse pathology ontology, skinbase, genotype, skin, gene, tissue, hair, mutant mouse strain, bio.tools is listed by: bio.tools
is listed by: Debian
is related to: Gene Ontology
has parent organization: University of Cambridge; Cambridge; United Kingdom
is parent organization of: Mouse Pathology Ontology
Lesion, Mutant mouse strain, Inbred mouse strain North American Hair Research Society ;
Ellison Medical Foundation ;
European Union QLRI-1999-00320;
European Union LSHG-CT-2006-037188;
NCI CA089713;
NCRR RR17436;
NIH AR49288
PMID:20587689
PMID:15623888
PMID:14681470
Except where otherwise noted, Creative Commons Attribution-NonCommercial-ShareAlike License, v3 Unported, Images on the database remain the property of the persons generously allowing their images to be used and are acknowledged within each record. Images should not be modified, Reproduced or disseminated without the express permission of the submitter. biotools:pathbase, nlx_151637 https://bio.tools/pathbase SCR_006141 Pathbase - European mutant mouse pathology database 2026-08-29 11:27:49 11
MRB - Mouse Resource Browser
 
Resource Report
Resource Website
1+ mentions
MRB - Mouse Resource Browser (RRID:SCR_005961) MRB data access protocol, data or information resource, database, registry, software resource, source code, web service Dynamic and interactive view of 222 world wide available mouse resources, classified in 22 categories. The massive generation of data has led to the propagation of mouse resources and databases and the concomitant need for formalized experimental descriptions, data standardization and database interoperability and integration. In this context and with these goals, information is collected through an online questionnaire and/or manual curation. All mouse resource data in MRB are broken up in four sections and presented in four tabs: * The General section/tab contains information such as URL(s), contact information, database description and categorization and related links. * The Ontologies & Standards tab indicates controlled vocabularies and data representation standards adopted by each resource, such as ontologies and minimum information standards. A hyperlink to an index of OBO and non-OBO ontologies can be found here; an index of minimum information standards can be found here. * The Technical tab holds technical information for each resource such as the server technology used, relational database management system(s) utilized, programming language(s) of implementation, schema descriptive documents or actual database dumps and most importantly information on each resource''s programmatic access, the integration and interoperability services. Additionally and through the integration with Molgenis, MRB is capable of generating a SOAP API for hosted resources. * The final section on Database Description Framework (DDF) Criteria, describes the compliance of each resource to the CASIMIR database criteria, which aim to capture key technical data about a database in a formal framework. All data in MRB are freely available to interested users through downloadable weekly database dumps. Programmatic access to some of MRB''s data is feasible via MRB''s SOAP web service. MRB is the front end of a relational, fully normalized PostgreSQL database. The source code is available under the GNU general public license (GPL) as a binary download and via cvs. registry, experimental description, data standardization, database interoperability, integration, minimum information standard, ontology, standard has parent organization: BSRC Al. Fleming; East Attica; Greece European Union LSHG-CT-2006-037811 Free, Source code is available under the GNU general public license., The community can contribute to this resource nlx_151623 SCR_005961 Mouse Resource Browser (MRB), Mouse Resource Browser 2026-08-29 11:27:48 2
STARNET
 
Resource Report
Resource Website
1+ mentions
STARNET (RRID:SCR_025238) STARNET data access protocol, software resource, source code, web service Web interactive browser to visualize data and perform gene set enrichment analysis along with gene and SNP lookup. Web interface used to query STARNET datasets and downstream analysis which includes RNAseq from 7 tissues: blood, free internal mammary artery (MAM), atherosclerotic aortic root (AOR), subcutaneous fat (SF), visceral abdominal fat (VAF), skeletal muscle (SKLM), and liver (LIV). Paired SNP genotyping data is included and utilized for tissue expression quantitative trait loci (eQTL), CAD heritability (H2), co-expression networks and gene regulatory networks. cross-tissue co-expression analysis, STARNET multitissue gene expression data, cardiovascular disease patients, American Heart Association ;
AstraZeneca ;
European Union ;
Federal German Ministries ;
Heart Lung Foundation ;
ModulMax ;
New South Wales health ;
NHLBI HL138193;
NHLBI PO1 HL28481;
NHLBI R01 HL144651;
NHLBI R01 HL147883;
NHLBI R01HL125863;
NHLBI R01HL130423;
NHLBI R01HL135093;
NHLBI R01HL148167;
NIDDK R01 DK117850;
Swedish Research Council
PMID:36276926 Free, Freely available https://github.com/skoplev/starnet SCR_025238 Stockholm-Tartu Atherosclerosis Reverse Networks Engineering Task 2026-08-29 11:34:00 6
Pathogens Portal Norway
 
Resource Report
Resource Website
Pathogens Portal Norway (RRID:SCR_025641) data or information resource, disease-related portal, portal, topical portal Portal provides information about available datasets, resources, tools, and services related to pandemic preparedness in Norway. Portal gives researchers, clinicians and policymakers access to collection of biomolecular data about pathogens. Norway, pandemic preparedness in Norway, pandemic data, pandemic, datasets, resources, tools, services, is related to: Pathogens Portal Netherlands ELIXIR Norway ;
European Union
Free, Freely available SCR_025641 2026-08-29 11:34:23 0
mirEX
 
Resource Report
Resource Website
10+ mentions
mirEX (RRID:SCR_006060) mirEX analysis service resource, atlas, data analysis service, data or information resource, database, production service resource, service resource mirEX is a comprehensive platform for comparative analysis of primary microRNA expression data. quantitative real-time PCR-based gene expression profiles are stored in a universal and expandable database scheme and wrapped by an intuitive user-friendly interface. A new way of accessing gene expression data in mirEX includes a simple mouse operated querying system and dynamic graphs for data mining analyses. In contrast to other publicly available databases, the mirEX interface allows a simultaneous comparison of expression levels between various microRNA genes in diverse organs and developmental stages. Currently, mirEX integrates information about the expression profile of 190 Arabidopsis thaliana pri-miRNAs in seven different developmental stages: seeds, seedlings and various organs of mature plants. Additionally, by providing RNA structural models, publicly available deep sequencing results, experimental procedure details and careful selection of auxiliary data in the form of web links, mirEX can function as a one-stop solution for Arabidopsis microRNA information. This database aims to be useful to anyone investigating the role of microRNAs in shaping plant development, organ formation and response to different biotic and abiotic stresses. To start exploring the database just press the "Browse Atlas" button or search for a particular microRNA record by typing at least two numbers from its ID in the window. microrna gene expression, microrna, gene expression, gene, organ, developmental stage, plant, seed, seedling, mature plant, pri-mirna, biotic stress, abiotic stress, organ formation, primer, cdna has parent organization: Adam Mickiewicz University in Poznan; Poznan; Poland Foundation for Polish Science ;
European Union ;
Regional Development Fund MPD 2010/3;
Polish Ministry of Science and Higher Education 3011/B/P01/2009/37
PMID:22013167 nlx_151462 http://bioinfo.amu.edu.pl/mirex SCR_006060 2026-08-29 11:22:30 10
UMD-BRCA1/ BRCA2 databases
 
Resource Report
Resource Website
10+ mentions
UMD-BRCA1/ BRCA2 databases (RRID:SCR_006128) UMD-BRCA1/ BRCA2 databases data or information resource, data repository, database, service resource, storage service resource The UMD-BRCA1/BRCA2 databases have been set up in a joined national effort through the network of 16 diagnostic laboratories to provide up-to-date information about mutations of the BRCA1 and BRCA2 genes identified in patients with breast and/or ovarian cancer. These databases currently contain published and unpublished information about the BRCA1/BRCA2 mutations reported in French diagnostic laboratories. This database includes 28 references and 5530 mutations (1440 different mutations and 786 protein variants) The databases of BRCA1 and BRCA2 mutations were built using the Universal Mutation Database tool. For each mutation, information is provided at several levels: * at the gene level: exon and codon number, wild type and mutant codon, mutation event, mutation name and, * at the protein level: wild type and mutant amino acid, binding domain, affected domain. If you want to submit a mutation, please contact R. Lidereau., S. Caputo. or E. Rouleau. cancer, gene, mutation, exon, codon, wild type, mutant, mutation, protein, amino acid, binding domain, affected domain, brca1, brca2, variant, polymorphism, unclassified variant, unknown variant, female, woman, bio.tools is listed by: Debian
is listed by: bio.tools
has parent organization: National Institute of Health and Medical Research; Rennes; France
Breast cancer, Ovarian cancer French National Cancer Institute ;
European Union FP7/2007-2013;
Association dAide a la Recherche Cancerologique de Saint Cloud
PMID:22144684 The UMD- BRCA1 Locus Specific Databases constitute the intellectual property of the curators of the database. Any unauthorized copying, Storage or distribution of this material without written permission from the curators would lead to copyright infringement with possible ensuing litigation. biotools:brca_share, nlx_151608 https://bio.tools/brca_share SCR_006128 UMD-BRCA1 mutations database, UMD-BRCA1 / BRCA2 databases, UMD-BRCA1/BRCA2 databases 2026-08-29 11:22:31 26
MatrixDB
 
Resource Report
Resource Website
50+ mentions
MatrixDB (RRID:SCR_001727) MatrixDB data or information resource, database, production service resource, service resource Freely available database focused on interactions established by extracellular proteins and polysaccharides, taking into account the multimeric nature of the extracellular proteins (e.g. collagens, laminins and thrombospondins are multimers). MatrixDB is an active member of the International Molecular Exchange (IMEx) consortium and has adopted the PSI-MI standards for annotating and exchanging interaction data. It includes interaction data extracted from the literature by manual curation, and offers access to relevant data involving extracellular proteins provided by the IMEx partner databases through the PSICQUIC webservice, as well as data from the Human Protein Reference Database. The database reports mammalian protein-protein and protein-carbohydrate interactions involving extracellular molecules. Interactions with lipids and cations are also reported. MatrixDB is focused on mammalian interactions, but aims to integrate interaction datasets of model organisms when available. MatrixDB provides direct links to databases recapitulating mutations in genes encoding extracellular proteins, to UniGene and to the Human Protein Atlas that shows expression and localization of proteins in a large variety of normal human tissues and cells. MatrixDB allows researchers to perform customized queries and to build tissue- and disease-specific interaction networks that can be visualized and analyzed with Cytoscape or Medusa. Statistics (2013): 2283 extracellular matrix interactions including 2095 protein-protein and 169 protein-glycosaminoglycan interactions. extracellular, protein fragment, biomolecule, cation, cleavage, collagen, glycosaminoglycan, human, interaction, laminin, lipid, mammalian, matricryptin, matrikin, matrix, molecule, monomer, mulimerization, multimer, polysaccharide, protein, protein-carbohydrate interaction, protein-protein interaction, recognition, thrombospondin, interactome, extracellular protein, protein-polysaccharide interaction, extracellular interaction, molecular interaction, model organism, inorganic, small molecule-protein, small molecule, extracellular matrix protein, protein-glycosaminoglycan interaction, bio.tools, FASEB list is listed by: re3data.org
is listed by: bio.tools
is listed by: Debian
is related to: IMEx - The International Molecular Exchange Consortium
is related to: Gene Ontology
is related to: PSI-MI
is related to: HPRD - Human Protein Reference Database
is related to: Interaction Reference Index
is related to: ConsensusPathDB
is related to: IMEx - The International Molecular Exchange Consortium
is related to: PSICQUIC Registry
is related to: IntAct
has parent organization: Claude Bernard University Lyon 1; Lyon; France
European Union contract FP7-HEALTH-2007-223411 PMID:20852260
PMID:19147664
THIS RESOURCE IS NO LONGER IN SERVICE biotools:matrixdb, r3d100010672, nif-0000-10226 https://bio.tools/matrixdb, https://doi.org/10.17616/R3M03H http://matrixdb.ibcp.fr/ SCR_001727 MatrixDB: Extracellular Matrix Interactions Database, Extracellular Matrix Interactions Database 2026-08-29 11:20:49 95
Biocatalogue - The Life Science Web Services Registry
 
Resource Report
Resource Website
1+ mentions
Biocatalogue - The Life Science Web Services Registry (RRID:SCR_001679) BioCatalogue data access protocol, data or information resource, database, software resource, web service Crowd-curated catalog of life sciences Web services with over 2400 service entries, thereby enabling users (people and programs) to discover and use these services easily. It provides a platform with several (standardized) interfaces and a suite of tools for registration of services by the community of users as well as empowers the community to extend and enhance the system. BioCatalogue provides a centralized biological web services market place which is accessible to the world as it is searchable and indexable to search engines. Additionally, it provides a quality of service standard for biological web services thereby enabling services to be classified and checked for availability, reliability and other quality measures. Primary goals: * Provide a single registration point for Web Service providers and a single search site for scientists and developers. * Providers, Expert curators and Users will provide oversight, monitor the catalog and provide high quality annotations for services. * BioCatalogue is a place where the community can find contacts and meet the experts and maintainers of these services. biological, web, life science, programmatic access, bioinformatics, registry, annotation, bio.tools is listed by: bio.tools
is listed by: Debian
is related to: MetaLocGramN
is related to: myExperiment
is related to: bioDBcore
has parent organization: European Bioinformatics Institute
has parent organization: University of Manchester; Manchester; United Kingdom
European Union LHSG-CT-2004-512092;
EMBO ASTF 338.00-2009
PMID:20484378 THIS RESOURCE IS NO LONGER IN SERVICE biotools:biocatalogue, nif-0000-10167 https://bio.tools/biocatalogue SCR_001679 Biocatalog 2026-08-29 11:21:00 7
Kidney and Urinary Pathway Knowledge Base
 
Resource Report
Resource Website
1+ mentions
Kidney and Urinary Pathway Knowledge Base (RRID:SCR_001746) KUPKB analysis service resource, data analysis service, data or information resource, data repository, data set, production service resource, service resource, storage service resource A collection of omics datasets (mRNA, proteins and miRNA) that have been extracted from PubMed and other related renal databases, all related to kidney physiology and pathology giving KUP biologists the means to ask queries across many resources in order to aggregate knowledge that is necessary for answering biological questions. Some microarray raw datasets have also been downloaded from the Gene Expression Omnibus and analyzed by the open-source software GeneArmada. The Semantic Web technologies, together with the background knowledge from the domain's ontologies, allows both rapid conversion and integration of this knowledge base. SPARQL endpoint http://sparql.kupkb.org/sparql The KUPKB Network Explorer will help you visualize the relationships among molecules stored in the KUPKB. A simple spreadsheet template is available for users to submit data to the KUPKB. It aims to capture a minimal amount of information about the experiment and the observations made. kidney, urinary, urine, pathway, molecule, visualizer, gene, protein, mirna, metabolite, mrna, microarray, ortholog, rdf, renal cell, anatomy, animal model, disease, sparql, proteomics, ontology, biomarker, gene expression, physiology, pathology is related to: NIDDK Information Network (dkNET)
is related to: Gene Expression Omnibus
is related to: Gene Ontology
is related to: KEGG
has parent organization: University of Manchester; Manchester; United Kingdom
has parent organization: National Institute of Health and Medical Research; Rennes; France
Kidney disease European Union ;
FP7 ;
ICT-2007.4.4 e-LICO project
PMID:21624162 THIS RESOURCE IS NO LONGER IN SERVICE. nlx_154134 http://www.e-lico.eu/kupkb SCR_001746 Kidney & Urinary Pathway Knowledge Base 2026-08-29 11:20:49 2
Genes to Cognition - Biological Resources
 
Resource Report
Resource Website
1+ mentions
Genes to Cognition - Biological Resources (RRID:SCR_001675) G2C Biological Resources biomaterial supply resource, material resource, organism supplier Biological resources, including gene-targeting vectors, ES cell lines, antibodies, and transgenic mice, generated for its phenotyping pipeline as part of the Genes to Cognition research program are freely-available to interested researchers. Available Transgenic Mouse Lines: *Hras1 (H-ras) knockout,C57BL/6J *Dlg4 (PSD-95) knockout,129S5 *Dlg4 (PSD-95) knockout,C57BL/6J *Dlg3 (SAP102) knockout with hprt mutation,129S5 *Dlg3 (SAP102) knockout (wild-type for hprt,C57BL/6J *Syngap1 (SynGAP) knockout (from 8.24 clone), C57BL/6J *Dlg4 (PSD-95) guanylate kinase domain deletion, C57BL/6J *Ptk2 (FAK) knockout,C57BL/6J transgenic, mutant mouse strain, c57bl/6j, 129s5, transgenic mouse line, vector, es cell line, transgenic mouse is listed by: One Mind Biospecimen Bank Listing
has parent organization: University of Edinburgh; Scotland; United Kingdom
Wellcome Trust ;
MRC ;
BBSRC ;
Gatsby Charitable Foundation ;
Human Frontiers Science Programme ;
European Union ;
Framework Programme ;
EPSRC ;
NSF
Free, Freely Available nif-0000-10163 http://www.genes2cognition.org/mice_resources/ http://www.genes2cognition.org/resources.html SCR_001675 G2C Mice Resources, G2C Biological Resources, G2C-Biological Resources, G2C - Biological Resources 2026-08-29 11:20:48 2
Functional Anatomy of the Cerebro-Cerebellar System (FACCS)
 
Resource Report
Resource Website
Functional Anatomy of the Cerebro-Cerebellar System (FACCS) (RRID:SCR_001661) FACCS analysis service resource, data analysis service, data or information resource, data repository, database, production service resource, service resource, storage service resource Public neuroscience database providing a collection of published data describing structure and structure-function relationships in one of the largest projection systems of the brain: the cerebro-cerebellar system. It also gives access to a suite of tools that allow the user to visualize and analyze any selected combination of data sets. Contact them if you are interested in contributing data. The overall goal is to improve communication of results and permit re-use of previously published data in new contexts. FACCS is a part of the Rat Brain WorkBench, a new research and development project funded by The Research Council of Norway, the Centre for Molecular Biology and Neuroscience, and the European Union. The project is directed by Jan G. Bjaalie, Centre for Molecular Biology and Neuroscience & Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway. axonal tracer, axon tracing, brain, cerebellum, cerebral cortex, cerebro-cerebellar function, cerebro-cerebellar structure, cerebro-cerebellar system, injection, injection site, labeled cells, labeled fibers, pontine nuclear complex, pontine nuclei, video, cerebellar cortex has parent organization: University of Oslo; Oslo; Norway Research Council of Norway ;
Centre for Molecular Biology and Neuroscience ;
European Union
PMID:17426352
PMID:16344144
THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-02317 SCR_001661 Functional Anatomy of the Cerebro-Cerebellar System 2026-08-29 11:20:59 0
InteroPorc
 
Resource Report
Resource Website
1+ mentions
InteroPorc (RRID:SCR_002067) InteroPorc analysis service resource, data analysis service, data analysis software, data or information resource, data processing software, database, production service resource, service resource, software application, software resource, source code Automatic prediction tool to infer protein-protein interaction networks, it is applicable for lots of species using orthology and known interactions. The interoPORC method is based on the interolog concept and combines source interaction datasets from public databases as well as clusters of orthologous proteins (PORC) available on Integr8. Users can use this page to ask InteroPorc for all species present in Integr8. Some results are already computed and users can run InteroPorc to investigate any other species. Currently, the following databases are processed and merged (with datetime of the last available public release for each database used): IntAct, MINT, DIP, and Integr8. orthology, prediction, protein interaction, tool, sequenced genome, proteinprotein interaction, inferred interaction, molecular interaction, interaction, protein, bio.tools is listed by: bio.tools
is listed by: Debian
is related to: Integr8 : Access to complete genomes and proteomes
is related to: IntAct
is related to: MINT
is related to: Database of Interacting Proteins (DIP)
is related to: PSICQUIC Registry
has parent organization: CEA; Gif sur Yvette; France
European Union FELICS 021902 RII3;
Marie Curie Fellowship ;
French National Agency of Research ANR Biosys06_134823 SULFIRHOM;
French Atomic Energy Commission
PMID:18508856 Open unspecified license, Acknowledgement requested nif-0000-20816, biotools:interoporc https://bio.tools/interoporc SCR_002067 InteroPorc: Automatic molecular interaction predictions, Automatic molecular interaction predictions 2026-08-29 11:21:10 6

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