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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_Y758
Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Proper citation: RRID:CVCL_Y758 Copy
https://web.expasy.org/cellosaurus/CVCL_GY32
Organism: Homo sapiens (Human)
Disease: Hereditary persistence of fetal hemoglobin
Category: Transformed cell line
Proper citation: Coriell Cat# GM23883, RRID:CVCL_GY32 Copy
https://web.expasy.org/cellosaurus/CVCL_Y765
Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Proper citation: RRID:CVCL_Y765 Copy
https://web.expasy.org/cellosaurus/CVCL_Y759
Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Proper citation: RRID:CVCL_Y759 Copy
https://web.expasy.org/cellosaurus/CVCL_Y762
Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Proper citation: Coriell Cat# GM23847, RRID:CVCL_Y762 Copy
https://web.expasy.org/cellosaurus/CVCL_U550
Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Transformed cell line
Proper citation: Coriell Cat# GM23832, RRID:CVCL_U550 Copy
https://web.expasy.org/cellosaurus/CVCL_GY32
Organism: Homo sapiens (Human)
Disease: Hereditary persistence of fetal hemoglobin
Category: Transformed cell line
Proper citation: RRID:CVCL_GY32 Copy
https://web.expasy.org/cellosaurus/CVCL_5T25
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: Coriell Cat# GM23873, RRID:CVCL_5T25 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ54
Organism: Homo sapiens (Human)
Disease: Wolff-Parkinson-White syndrome
Category: Transformed cell line
Proper citation: RRID:CVCL_HQ54 Copy
https://web.expasy.org/cellosaurus/CVCL_U553
Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Transformed cell line
Proper citation: RRID:CVCL_U553 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: Coriell Cat# GM23842, RRID:CVCL_IX39 Copy
https://web.expasy.org/cellosaurus/CVCL_BW28
Organism: Homo sapiens (Human)
Disease: Rett syndrome
Category: Transformed cell line
Proper citation: RRID:CVCL_BW28 Copy
https://web.expasy.org/cellosaurus/CVCL_CX82
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_CX82 Copy
https://web.expasy.org/cellosaurus/CVCL_Y779
Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Proper citation: RRID:CVCL_Y779 Copy
https://web.expasy.org/cellosaurus/CVCL_Y775
Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Comments: Population: Caucasian; Greek/Portuguese.
Proper citation: RRID:CVCL_Y775 Copy
https://web.expasy.org/cellosaurus/CVCL_Y778
Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Proper citation: Coriell Cat# GM24018, RRID:CVCL_Y778 Copy
https://web.expasy.org/cellosaurus/CVCL_BX15
Organism: Homo sapiens (Human)
Disease: Central core disease
Category: Transformed cell line
Proper citation: RRID:CVCL_BX15 Copy
https://web.expasy.org/cellosaurus/CVCL_5T32
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: Coriell Cat# GM23905, RRID:CVCL_5T32 Copy
https://web.expasy.org/cellosaurus/CVCL_Y775
Organism: Homo sapiens (Human)
Disease: Ornithine carbamoyltransferase deficiency disease
Category: Transformed cell line
Comments: Population: Caucasian; Greek/Portuguese.
Proper citation: Coriell Cat# GM24010, RRID:CVCL_Y775 Copy
https://web.expasy.org/cellosaurus/CVCL_4F85
Organism: Homo sapiens (Human)
Disease: Medium-chain acyl-CoA dehydrogenase deficiency
Category: Transformed cell line
Proper citation: RRID:CVCL_4F85 Copy
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