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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_N148
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Pacific., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel.
Proper citation: RRID:CVCL_N148 Copy
https://web.expasy.org/cellosaurus/CVCL_AM52
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.
Proper citation: RRID:CVCL_AM52 Copy
https://web.expasy.org/cellosaurus/CVCL_5P22
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5P22 Copy
https://web.expasy.org/cellosaurus/CVCL_AM42
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.
Proper citation: Coriell Cat# GM10526, RRID:CVCL_AM42 Copy
https://web.expasy.org/cellosaurus/CVCL_5P20
Organism: Homo sapiens (Human)
Disease: Dyggve-Melchior-Clausen syndrome
Category: Finite cell line
Comments: Population: Pakistani.
Proper citation: Coriell Cat# GM10568, RRID:CVCL_5P20 Copy
https://web.expasy.org/cellosaurus/CVCL_AM52
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.
Proper citation: Coriell Cat# GM10537, RRID:CVCL_AM52 Copy
https://web.expasy.org/cellosaurus/CVCL_N151
Organism: Homo sapiens (Human)
Disease: Sjogren-Larsson syndrome
Category: Finite cell line
Comments: Population: South American (Andes)., Part of: Human variation panel.
Proper citation: RRID:CVCL_N151 Copy
https://web.expasy.org/cellosaurus/CVCL_AM46
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.
Proper citation: Coriell Cat# GM10531, RRID:CVCL_AM46 Copy
https://web.expasy.org/cellosaurus/CVCL_0Q12
Organism: Homo sapiens (Human)
Disease: Marfan syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM10559, RRID:CVCL_0Q12 Copy
https://web.expasy.org/cellosaurus/CVCL_5P19
Organism: Homo sapiens (Human)
Disease: Hypogonadotropic hypogonadism with anosmia
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5P19 Copy
https://web.expasy.org/cellosaurus/CVCL_7502
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Pacific., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel.
Proper citation: Coriell Cat# GM10540, RRID:CVCL_7502 Copy
https://web.expasy.org/cellosaurus/CVCL_9S97
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 47,XY,+i(12)(pter->p10::p10->pter) [37]; 46,XY [13] (Coriell=GM10679)., Population: Caucasian.
Proper citation: Coriell Cat# GM10679, RRID:CVCL_9S97 Copy
https://web.expasy.org/cellosaurus/CVCL_1Y47
Organism: Homo sapiens (Human)
Disease: Sandhoff disease
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM10720, RRID:CVCL_1Y47 Copy
https://web.expasy.org/cellosaurus/CVCL_AD72
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_AD72 Copy
https://web.expasy.org/cellosaurus/CVCL_1Y47
Organism: Homo sapiens (Human)
Disease: Sandhoff disease
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_1Y47 Copy
https://web.expasy.org/cellosaurus/CVCL_1R98
Organism: Homo sapiens (Human)
Disease:
Category: Hybrid cell line
Comments: Characteristics: Hybrid for chromosomes 15 and 17 mapping (PubMed=9441767)., Group: Human/rodent somatic cell hybrid.
Proper citation: Coriell Cat# GM10659, RRID:CVCL_1R98 Copy
https://web.expasy.org/cellosaurus/CVCL_N152
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples.
Proper citation: Coriell Cat# GM10647, RRID:CVCL_N152 Copy
https://web.expasy.org/cellosaurus/CVCL_1R97
Organism: Homo sapiens (Human)
Disease:
Category: Hybrid cell line
Comments: Characteristics: Hybrid for chromosome 17 mapping (PubMed=9441767)., Group: Human/rodent somatic cell hybrid.
Proper citation: RRID:CVCL_1R97 Copy
https://web.expasy.org/cellosaurus/CVCL_DB76
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_DB76 Copy
https://web.expasy.org/cellosaurus/CVCL_AD73
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM10710, RRID:CVCL_AD73 Copy
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