FINDbase specifications


Unique identifier OMICS_04949
Name FINDbase
Alternative name Frequency of INherited Disorders database
Restrictions to use None
Community driven No
Data access Browse
User data submission Allowed
Maintained Yes


  • Primates
    • Homo sapiens


  • person_outline George Patrinos

Publications for Frequency of INherited Disorders database

FINDbase citations


A pan cancer analysis of prognostic genes

PMCID: 4815555
PMID: 27047702
DOI: 10.7717/peerj.1499

[…] actors which have clinical significance, and many different resources now allow researchers to identify if a protein of interest has clinical implications, including OMIM, dbSNP, ClinVar, cBioPortal, FINDbase, and others (; ; ; ). Despite this, it currently is not possible to find comprehensive lists of genes which are associated with survival in different cancers. Using recently available RNA-SEQ […]


The 2014 Nucleic Acids Research Database Issue and an updated NAR online Molecular Biology Database Collection

Nucleic Acids Res
PMCID: 3965027
PMID: 24316579
DOI: 10.1093/nar/gkt1282

[…] ants, indels and copy-number variants; and the Database of Genomic Variants (DGV) at the Toronto’s Centre for Applied Genomics (). There are also several more specialized databases (canSAR, DriverDB, FINDBase, HbVar, Lynx, NECTAR, Progenetix) that cover genetic defects leading to various human diseases, including cancer. In addition, three separate databases, Selectome, dbPSHP and 1000 Genomes Sel […]

FINDbase institution(s)
University of Patras, Faculty of Engineering, Department of Computer Engineering and Informatics, Patras, Greece; Department of Pharmacy, School of Health Sciences, University of Patras, Patras, Greece; Erasmus University Medical Center, Faculty of Medicine and Health Sciences, Department of Bioinformatics, Rotterdam, The Netherlands; University of Malta, Faculty of Medicine and Surgery, Department of Physiology and Biochemistry, Malta; Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Laboratory of Molecular Biomedicine, Belgrade, Serbia; The Golden Helix Foundation, London, UK; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland; Department of Experimental Medical Science, Lund University, Lund, Sweden; Department of Computer and Informatics Engineering, Technological Educational Institute of Western Greece, Patras, Greece
FINDbase funding source(s)
Supported by European Commission [GEN2PHEN (FP7-200754), RDCONNECT (FP7-305444), SEE DRUG (FP7-285950), UPGx (H2020-668353) and SERBORDISInn (FP7-316088)]; Greek State grant [EAvEK 2014- 2020; ELIXIR GR)]; Serbian State grant [III 41004 MESTD RS] and Golden Helix Foundation (UK).

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