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URL: https://www.hmtphenome.uniba.it
Proper Citation: HmtPhenome (RRID:SCR_017289)
Description: Collection of data about variants, genes, phenotypes and diseases involved in mitochondrial functionality. Users can search for variant position, gene, phenotype or disease and retrieve all related information through integrated network of biological entities.
Resource Type: data or information resource, data processing software, data visualization software, database, network graph visualization software, service resource, software application, software resource
Defining Citation: DOI:10.1101/660282
Keywords: mitochondria, variant, gene, function, phenotype, data
Availability: Free, Freely available
Resource Name: HmtPhenome
Resource ID: SCR_017289
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Source: SciCrunch Registry (RRID:SCR_005400)
Description: Interactive portal for finding and submitting biomedical resources. Resources within SciCrunch have assigned RRIDs which are used to cite resources in scientific manuscripts. SciCrunch Registry, formerly NIF Registry, provides resources catalog. Allows to add new resources. Allows edit existing resources after registration. Curators are tasked with identifying and registering resources, examining data, writing configuration files to index and display data and keeping contents current.
URL: https://rrid.site/rin/sources/SCR_005400
