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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_0Q59
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_0Q59 Copy
https://web.expasy.org/cellosaurus/CVCL_2T29
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_2T29 Copy
https://web.expasy.org/cellosaurus/CVCL_0Q59
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM07081, RRID:CVCL_0Q59 Copy
https://web.expasy.org/cellosaurus/CVCL_X048
Organism: Homo sapiens (Human)
Disease: Tetralogy of Fallot
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;17)(p11.2;p11.2).arr(1-22,X)x2 (Coriell=GM07151)., Population: Caucasian.
Proper citation: Coriell Cat# GM07151, RRID:CVCL_X048 Copy
https://web.expasy.org/cellosaurus/CVCL_5N59
Organism: Homo sapiens (Human)
Disease: Holoprosencephaly
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_5N59 Copy
https://web.expasy.org/cellosaurus/CVCL_2Y98
Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_2Y98 Copy
https://web.expasy.org/cellosaurus/CVCL_X141
Organism: Homo sapiens (Human)
Disease: Sporadic retinoblastoma
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_X141 Copy
https://web.expasy.org/cellosaurus/CVCL_4D92
Organism: Homo sapiens (Human)
Disease: Ring chromosome 14 syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_4D92 Copy
https://web.expasy.org/cellosaurus/CVCL_5N63
Organism: Homo sapiens (Human)
Disease: Wilms tumor
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5N63 Copy
https://web.expasy.org/cellosaurus/CVCL_5N62
Organism: Homo sapiens (Human)
Disease: Developmental delay
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM07412, RRID:CVCL_5N62 Copy
https://web.expasy.org/cellosaurus/CVCL_F668
Organism: Homo sapiens (Human)
Disease: Hydatidiform mole
Category: Cancer cell line
Comments: Population: Southeast Asian; Filipino.
Proper citation: RRID:CVCL_F668 Copy
https://web.expasy.org/cellosaurus/CVCL_5P62
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_5P62 Copy
https://web.expasy.org/cellosaurus/CVCL_5L21
Organism: Homo sapiens (Human)
Disease: Deletion 18q syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM12025, RRID:CVCL_5L21 Copy
https://web.expasy.org/cellosaurus/CVCL_5P62
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM12013, RRID:CVCL_5P62 Copy
https://web.expasy.org/cellosaurus/CVCL_5L21
Organism: Homo sapiens (Human)
Disease: Deletion 18q syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5L21 Copy
https://web.expasy.org/cellosaurus/CVCL_5P63
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM12074, RRID:CVCL_5P63 Copy
https://web.expasy.org/cellosaurus/CVCL_5P63
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5P63 Copy
https://web.expasy.org/cellosaurus/CVCL_5P64
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM12218, RRID:CVCL_5P64 Copy
https://web.expasy.org/cellosaurus/CVCL_U535
Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_U535 Copy
https://web.expasy.org/cellosaurus/CVCL_1K30
Organism: Homo sapiens (Human)
Disease: Charcot-Marie-Tooth disease type 1A
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_1K30 Copy
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