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URL: http://phencode.bx.psu.edu/
Proper Citation: PhenCode (RRID:SCR_010799)
Description: A collaborative project to better understand the relationship between genotype and phenotype in humans that connects human phenotype and clinical data in various locus-specific mutation databases (LSDBs) with data on genome sequences, evolutionary history, and function in the UCSC Genome Browser. PhenCode is a collaboration among researchers at Penn State, UC Santa Cruz, and locus experts at other institutions.
Abbreviations: PhenCode
Synonyms: PhenCode: Paving the Path between Phenotype and Genome, Phenotypes for ENCODE
Resource Type: data or information resource, database
Defining Citation: PMID:17326095
Keywords: genotype, phenotype, mutation
Availability: Acknowledgement requested, Free
Resource Name: PhenCode
Resource ID: SCR_010799
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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
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