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_4T51
Organism: Homo sapiens (Human)
Disease: Ullrich congenital muscular dystrophy
Category: Transformed cell line
Proper citation: RRID:CVCL_4T51 Copy
https://web.expasy.org/cellosaurus/CVCL_M916
Organism: Homo sapiens (Human)
Disease: Charcot-Marie-Tooth disease type 1B
Category: Transformed cell line
Proper citation: RRID:CVCL_M916 Copy
https://web.expasy.org/cellosaurus/CVCL_BX08
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian; British/French.
Proper citation: Coriell Cat# GM23773, RRID:CVCL_BX08 Copy
https://web.expasy.org/cellosaurus/CVCL_AY86
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: RRID:CVCL_AY86 Copy
https://web.expasy.org/cellosaurus/CVCL_Y746
Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Proper citation: RRID:CVCL_Y746 Copy
https://web.expasy.org/cellosaurus/CVCL_GT01
Organism: Homo sapiens (Human)
Disease: Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Category: Transformed cell line
Proper citation: RRID:CVCL_GT01 Copy
https://web.expasy.org/cellosaurus/CVCL_BW11
Organism: Homo sapiens (Human)
Disease: Charcot-Marie-Tooth disease
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM23750, RRID:CVCL_BW11 Copy
https://web.expasy.org/cellosaurus/CVCL_Y755
Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Proper citation: RRID:CVCL_Y755 Copy
https://web.expasy.org/cellosaurus/CVCL_BW13
Organism: Homo sapiens (Human)
Disease: Inclusion body myositis
Category: Transformed cell line
Proper citation: RRID:CVCL_BW13 Copy
https://web.expasy.org/cellosaurus/CVCL_U111
Organism: Homo sapiens (Human)
Disease: Anorexia nervosa
Category: Induced pluripotent stem cell
Comments: Population: Jewish.
Proper citation: Coriell Cat# GM23764, RRID:CVCL_U111 Copy
https://web.expasy.org/cellosaurus/CVCL_AY89
Organism: Homo sapiens (Human)
Disease: Argininosuccinic aciduria
Category: Transformed cell line
Proper citation: RRID:CVCL_AY89 Copy
https://web.expasy.org/cellosaurus/CVCL_BW24
Organism: Homo sapiens (Human)
Disease: Congenital fiber-type disproportion
Category: Finite cell line
Proper citation: Coriell Cat# GM23895, RRID:CVCL_BW24 Copy
https://web.expasy.org/cellosaurus/CVCL_GY33
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: RRID:CVCL_GY33 Copy
https://web.expasy.org/cellosaurus/CVCL_AY89
Organism: Homo sapiens (Human)
Disease: Argininosuccinic aciduria
Category: Transformed cell line
Proper citation: Coriell Cat# GM23845, RRID:CVCL_AY89 Copy
https://web.expasy.org/cellosaurus/CVCL_IX39
Organism: Homo sapiens (Human)
Disease: Presynaptic congenital myasthenic syndrome 6
Category: Transformed cell line
Comments: Population: Caucasian; Irish.
Proper citation: RRID:CVCL_IX39 Copy
https://web.expasy.org/cellosaurus/CVCL_BW24
Organism: Homo sapiens (Human)
Disease: Congenital fiber-type disproportion
Category: Finite cell line
Proper citation: RRID:CVCL_BW24 Copy
https://web.expasy.org/cellosaurus/CVCL_5T21
Organism: Homo sapiens (Human)
Disease: Isodicentric chromosome
Category: Transformed cell line
Proper citation: RRID:CVCL_5T21 Copy
https://web.expasy.org/cellosaurus/CVCL_GY34
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: RRID:CVCL_GY34 Copy
https://web.expasy.org/cellosaurus/CVCL_GY34
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: Coriell Cat# GM23885, RRID:CVCL_GY34 Copy
https://web.expasy.org/cellosaurus/CVCL_Y765
Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Proper citation: Coriell Cat# GM23864, RRID:CVCL_Y765 Copy
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