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Proper Citation: RettBASE: IRSF MECP2 Variation Database (RRID:SCR_001066)
Description: Database constructed by merging mutation and polymorphism data from the published literature pertaining to Rett syndrome and related clinical disorders, and by incorporating unpublished mutation and polymorphism data that have been submitted directly. RettBase is updated on a very frequent basis manually by curators to ensure the validity of the data submitted., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.
Synonyms: RettBase
Resource Type: data or information resource, database
Defining Citation: PMID:28544139
Keywords: genetics; metadata, polymorphism
Related Condition: Rett Syndrome
Availability: THIS RESOURCE IS NO LONGER IN SERVICE
Resource Name: RettBASE: IRSF MECP2 Variation Database
Resource ID: SCR_001066
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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
The data sets included in this resource are published in Kravitz et al, 2012. Distinct roles for direct and indirect pathway striatal neurons in reinforcement (Nat. Neurosci).
