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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_N206
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: South American (Brazil, Guyana, Venezuela)., Part of: Human variation panel.
Proper citation: RRID:CVCL_N206 Copy
https://web.expasy.org/cellosaurus/CVCL_V396
Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type Ia
Category: Transformed cell line
Proper citation: Coriell Cat# GM13289, RRID:CVCL_V396 Copy
https://web.expasy.org/cellosaurus/CVCL_V397
Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type Ia
Category: Transformed cell line
Proper citation: Coriell Cat# GM13290, RRID:CVCL_V397 Copy
https://web.expasy.org/cellosaurus/CVCL_V144
Organism: Homo sapiens (Human)
Disease: Von Hippel-Lindau syndrome
Category: Transformed cell line
Proper citation: RRID:CVCL_V144 Copy
https://web.expasy.org/cellosaurus/CVCL_BW64
Organism: Homo sapiens (Human)
Disease: D-bifunctional protein deficiency
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM13262, RRID:CVCL_BW64 Copy
https://web.expasy.org/cellosaurus/CVCL_4F70
Organism: Homo sapiens (Human)
Disease: Zellweger syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_4F70 Copy
https://web.expasy.org/cellosaurus/CVCL_GS82
Organism: Homo sapiens (Human)
Disease: Lipoid proteinosis of Urbach and Wiethe
Category: Finite cell line
Comments: Population: Caucasian; German.
Proper citation: Coriell Cat# GM13241, RRID:CVCL_GS82 Copy
https://web.expasy.org/cellosaurus/CVCL_2U25
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM13284, RRID:CVCL_2U25 Copy
https://web.expasy.org/cellosaurus/CVCL_GZ47
Organism: Homo sapiens (Human)
Disease: Congenital bilateral aplasia of the vas deferens
Category: Transformed cell line
Proper citation: RRID:CVCL_GZ47 Copy
https://web.expasy.org/cellosaurus/CVCL_GT65
Organism: Homo sapiens (Human)
Disease: Hereditary hemorrhagic telangiectasia
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_GT65 Copy
https://web.expasy.org/cellosaurus/CVCL_L931
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: African American., Part of: Human variation panel.
Proper citation: Coriell Cat# GM13293, RRID:CVCL_L931 Copy
https://web.expasy.org/cellosaurus/CVCL_L932
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: African American., Part of: Human variation panel.
Proper citation: Coriell Cat# GM17109, RRID:CVCL_L932 Copy
https://web.expasy.org/cellosaurus/CVCL_9R31
Organism: Homo sapiens (Human)
Disease: Neonatal adrenoleukodystrophy
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM13268, RRID:CVCL_9R31 Copy
https://web.expasy.org/cellosaurus/CVCL_4F69
Organism: Homo sapiens (Human)
Disease: Zellweger syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_4F69 Copy
https://web.expasy.org/cellosaurus/CVCL_1K72
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: Coriell Cat# GM13306, RRID:CVCL_1K72 Copy
https://web.expasy.org/cellosaurus/CVCL_9R95
Organism: Homo sapiens (Human)
Disease: Holt-Oram syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_9R95 Copy
https://web.expasy.org/cellosaurus/CVCL_GS82
Organism: Homo sapiens (Human)
Disease: Lipoid proteinosis of Urbach and Wiethe
Category: Finite cell line
Comments: Population: Caucasian; German.
Proper citation: RRID:CVCL_GS82 Copy
https://web.expasy.org/cellosaurus/CVCL_V145
Organism: Homo sapiens (Human)
Disease: Von Hippel-Lindau syndrome
Category: Transformed cell line
Proper citation: Coriell Cat# GM13257, RRID:CVCL_V145 Copy
https://web.expasy.org/cellosaurus/CVCL_1K70
Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type II
Category: Transformed cell line
Proper citation: RRID:CVCL_1K70 Copy
https://web.expasy.org/cellosaurus/CVCL_V397
Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type Ia
Category: Transformed cell line
Proper citation: RRID:CVCL_V397 Copy
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