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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_V339
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Finite cell line
Comments: Part of: Venezuelan Huntington disease kindreds subcollection.
Proper citation: Coriell Cat# GM04476, RRID:CVCL_V339 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_0L60
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: African American.
Proper citation: Coriell Cat# GM04599, RRID:CVCL_0L60 Copy
https://web.expasy.org/cellosaurus/CVCL_N019
Organism: Homo sapiens (Human)
Disease: Phosphoglycerate kinase 1 deficiency
Category: Transformed cell line
Comments: Population: Japanese., Part of: Human variation panel.
Proper citation: Coriell Cat# GM17053, RRID:CVCL_N019 Copy
https://web.expasy.org/cellosaurus/CVCL_DB60
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_DB60 Copy
https://web.expasy.org/cellosaurus/CVCL_9R20
Organism: Homo sapiens (Human)
Disease: Adrenoleukodystrophy
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM04496, RRID:CVCL_9R20 Copy
https://web.expasy.org/cellosaurus/CVCL_Y795
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM04603, RRID:CVCL_Y795 Copy
https://web.expasy.org/cellosaurus/CVCL_V473
Organism: Homo sapiens (Human)
Disease: Down syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_V473 Copy
https://web.expasy.org/cellosaurus/CVCL_GY22
Organism: Homo sapiens (Human)
Disease: Charcot-Marie-Tooth neuropathy X type 1
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_GY22 Copy
https://web.expasy.org/cellosaurus/CVCL_N019
Organism: Homo sapiens (Human)
Disease: Phosphoglycerate kinase 1 deficiency
Category: Transformed cell line
Comments: Population: Japanese., Part of: Human variation panel.
Proper citation: RRID:CVCL_N019 Copy
https://web.expasy.org/cellosaurus/CVCL_X119
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 47,XX,+del(2)(qter->p23) [38]; 47,XX,+2 [12] (Coriell=GM04513)., Population: Caucasian.
Proper citation: Coriell Cat# GM04513, RRID:CVCL_X119 Copy
https://web.expasy.org/cellosaurus/CVCL_7413
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Donor information: Established from monozygotic twin of GM04505 (Cellosaurus=CVCL_7412)., Population: Caucasian.
Proper citation: RRID:CVCL_7413 Copy
https://web.expasy.org/cellosaurus/CVCL_9Y80
Organism: Homo sapiens (Human)
Disease: Albright's hereditary osteodystrophy
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM04427, RRID:CVCL_9Y80 Copy
https://web.expasy.org/cellosaurus/CVCL_7413
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Donor information: Established from monozygotic twin of GM04505 (Cellosaurus=CVCL_7412)., Population: Caucasian.
Proper citation: Coriell Cat# GM04506, RRID:CVCL_7413 Copy
https://web.expasy.org/cellosaurus/CVCL_AA23
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_AA23 Copy
https://web.expasy.org/cellosaurus/CVCL_X306
Organism: Homo sapiens (Human)
Disease: Isodicentric chromosome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_X306 Copy
https://web.expasy.org/cellosaurus/CVCL_7409
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Donor information: Established from monozygotic twin of GM04502 (Cellosaurus=CVCL_F135).
Proper citation: RRID:CVCL_7409 Copy
https://web.expasy.org/cellosaurus/CVCL_V567
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Part of: Venezuelan Huntington disease kindreds subcollection.
Proper citation: RRID:CVCL_V567 Copy
https://web.expasy.org/cellosaurus/CVCL_0M36
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_0M36 Copy
https://web.expasy.org/cellosaurus/CVCL_4F50
Organism: Homo sapiens (Human)
Disease: Medium-chain acyl-CoA dehydrogenase deficiency
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_4F50 Copy
https://web.expasy.org/cellosaurus/CVCL_AK96
Organism: Homo sapiens (Human)
Disease: Retinitis pigmentosa
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM04562, RRID:CVCL_AK96 Copy
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