Searching the RRID Resource Information Network
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Cellosaurus is database indexing available cell lines from various collections: American Type Culture Collection (ATCC), Bioresource Collection and Research Center, Taiwan (BCRC), Banco de Células do Rio de Janeiro (BCRJ), CellBank Australia (CBA), Collection of Cell Lines in Veterinary Medicine (CCLV), Cell Lines Service (CLS), Coriell, Drosophila Genomics Resource Center (DGRC), Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (DSMZ), European Bank for induced pluripotent Stem Cells (EBiSC), European Collection of Authenticated Cell Cultures (ECACC), Interlab Cell Line Collection (ICLC), Institute for Fermentation Osaka (IFO), Istituto Zooprofilattico Sperimentale della Lombardia e dell'Emilia Romagna (IZSLER) biobank, Japanese Collection of Research Bioresources (JCRB) Cell Bank, Kunming Cell Bank of Type Culture Collection (KCB), Korean Cell Line Bank (KCLB), Millipore, National Cell Bank of Iran (NCBI_Iran), National Cancer Institute - Developmental Therapeutics Program (NCI-DTP), NINDS Human Cell and Data Repository (NHCDR), NIH AIDS Reagent Program (NIH-ARP), NISES, RIKEN Bioresource Center Cell Bank (RCB), Royan Stem Cell Bank (RSCB), Tick Cell Biobank (TCB), Tohoku University cell line catalog (TKG), and Ximbio.
https://web.expasy.org/cellosaurus/CVCL_7499
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM09918, RRID:CVCL_7499 Copy
https://web.expasy.org/cellosaurus/CVCL_FV59
Organism: Homo sapiens (Human)
Disease: Epidermolysis bullosa dystrophica
Category: Finite cell line
Comments: Population: Ecuadorian.
Proper citation: RRID:CVCL_FV59 Copy
https://web.expasy.org/cellosaurus/CVCL_8A52
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM09911, RRID:CVCL_8A52 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_UT44
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_UT44 Copy
https://web.expasy.org/cellosaurus/CVCL_FV60
Organism: Homo sapiens (Human)
Disease: Epidermolysis bullosa dystrophica
Category: Transformed cell line
Comments: Population: Ecuadorian.
Proper citation: Coriell Cat# GM09870, RRID:CVCL_FV60 Copy
https://web.expasy.org/cellosaurus/CVCL_AB08
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Jewish; Ashkenazi.
Proper citation: RRID:CVCL_AB08 Copy
https://web.expasy.org/cellosaurus/CVCL_7500
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_7500 Copy
https://web.expasy.org/cellosaurus/CVCL_N124
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; Portuguese., Part of: Human variation panel.
Proper citation: RRID:CVCL_N124 Copy
https://web.expasy.org/cellosaurus/CVCL_7498
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Human variation panel.
Proper citation: Coriell Cat# GM09869, RRID:CVCL_7498 Copy
https://web.expasy.org/cellosaurus/CVCL_IN27
Organism: Homo sapiens (Human)
Disease: Neonatal hemochromatosis
Category: Finite cell line
Comments: Population: Caucasian; Portuguese.
Proper citation: RRID:CVCL_IN27 Copy
https://web.expasy.org/cellosaurus/CVCL_FV59
Organism: Homo sapiens (Human)
Disease: Epidermolysis bullosa dystrophica
Category: Finite cell line
Comments: Population: Ecuadorian.
Proper citation: Coriell Cat# GM09865, RRID:CVCL_FV59 Copy
https://web.expasy.org/cellosaurus/CVCL_AA00
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM09944, RRID:CVCL_AA00 Copy
https://web.expasy.org/cellosaurus/CVCL_2T69
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_2T69 Copy
https://web.expasy.org/cellosaurus/CVCL_9S95
Organism: Homo sapiens (Human)
Disease: Developmental delay
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_9S95 Copy
https://web.expasy.org/cellosaurus/CVCL_5P08
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_5P08 Copy
https://web.expasy.org/cellosaurus/CVCL_AI96
Organism: Homo sapiens (Human)
Disease: Hepatocyte nuclear factor 4-alpha associated monogenic diabetes
Category: Transformed cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.
Proper citation: RRID:CVCL_AI96 Copy
https://web.expasy.org/cellosaurus/CVCL_AJ05
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.
Proper citation: RRID:CVCL_AJ05 Copy
https://web.expasy.org/cellosaurus/CVCL_N127
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Biotechnology: Used a source of control genomic DNA for USA forensic testing., Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples.
Proper citation: RRID:CVCL_N127 Copy
https://web.expasy.org/cellosaurus/CVCL_AJ06
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.
Proper citation: Coriell Cat# GM10059, RRID:CVCL_AJ06 Copy
https://web.expasy.org/cellosaurus/CVCL_AJ03
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.
Proper citation: Coriell Cat# GM10056, RRID:CVCL_AJ03 Copy
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The NIDDK Information Network (dkNET) serves the needs of basic and clinical investigators by providing seamless access to large pools of data and research resources relevant to the mission of The National Institute of Diabetes Digestive and Kidney Diseases (NIDDK). dkNET is hosted at University of California San Diego, and is supported by NIH NIDDK grant U24DK097771.
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