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_2U04
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: RRID:CVCL_2U04 Copy
https://web.expasy.org/cellosaurus/CVCL_N173
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Chinese., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples.
Proper citation: RRID:CVCL_N173 Copy
https://web.expasy.org/cellosaurus/CVCL_4F12
Organism: Homo sapiens (Human)
Disease: Rett syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_4F12 Copy
https://web.expasy.org/cellosaurus/CVCL_4F16
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: RRID:CVCL_4F16 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_4F26
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: RRID:CVCL_4F26 Copy
https://web.expasy.org/cellosaurus/CVCL_4F19
Organism: Homo sapiens (Human)
Disease: Rett syndrome
Category: Transformed cell line
Proper citation: RRID:CVCL_4F19 Copy
https://web.expasy.org/cellosaurus/CVCL_2N25
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM00403, RRID:CVCL_2N25 Copy
https://web.expasy.org/cellosaurus/CVCL_M921
Organism: Homo sapiens (Human)
Disease: Sandhoff disease
Category: Finite cell line
Comments: Population: Mexican., Part of: Human variation panel.
Proper citation: RRID:CVCL_M921 Copy
https://web.expasy.org/cellosaurus/CVCL_F125
Organism: Homo sapiens (Human)
Disease: Fanconi anemia, complementation group C
Category: Finite cell line
Comments: Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples.
Proper citation: RRID:CVCL_F125 Copy
https://web.expasy.org/cellosaurus/CVCL_7288
Organism: Homo sapiens (Human)
Disease: Hyperlipoproteinemia, type IIa
Category: Finite cell line
Comments: Population: Caucasian; French Canadian.
Proper citation: RRID:CVCL_7288 Copy
https://web.expasy.org/cellosaurus/CVCL_H131
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: RRID:CVCL_H131 Copy
https://web.expasy.org/cellosaurus/CVCL_V769
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 45,XX,der(13;22)(13qter->13q10::22q10->22qter) (Coriell=GM00392)., Population: Caucasian.
Proper citation: RRID:CVCL_V769 Copy
https://web.expasy.org/cellosaurus/CVCL_J105
Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Transformed cell line
Proper citation: RRID:CVCL_J105 Copy
https://web.expasy.org/cellosaurus/CVCL_2N25
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_2N25 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JD74
Organism: Homo sapiens (Human)
Disease: Fanconi anemia
Category: Finite cell line
Proper citation: Coriell Cat# GM00391, RRID:CVCL_JD74 Copy
https://web.expasy.org/cellosaurus/CVCL_V768
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(4;11)(4pter->4q23::11q11->11qter;11pter->11q11::4q23->4qter) (Coriell=GM00380)., Population: Caucasian.
Proper citation: Coriell Cat# GM00380, RRID:CVCL_V768 Copy
https://web.expasy.org/cellosaurus/CVCL_V769
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 45,XX,der(13;22)(13qter->13q10::22q10->22qter) (Coriell=GM00392)., Population: Caucasian.
Proper citation: Coriell Cat# GM00392, RRID:CVCL_V769 Copy
https://web.expasy.org/cellosaurus/CVCL_Y983
Organism: Homo sapiens (Human)
Disease: Nephropathic cystinosis
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_Y983 Copy
https://web.expasy.org/cellosaurus/CVCL_J105
Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Transformed cell line
Proper citation: Coriell Cat# GM00467, RRID:CVCL_J105 Copy
https://web.expasy.org/cellosaurus/CVCL_M921
Organism: Homo sapiens (Human)
Disease: Sandhoff disease
Category: Finite cell line
Comments: Population: Mexican., Part of: Human variation panel.
Proper citation: Coriell Cat# GM00470, RRID:CVCL_M921 Copy
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