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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_E770
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Indian; Tamil., Part of: 10th International Histocompatibility Workshop (10IHW) cell line panel.
Proper citation: ECACC Cat# 94122027, RRID:CVCL_E770 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_8Y12
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 00051801, RRID:CVCL_8Y12 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_8Y14
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 00110317, RRID:CVCL_8Y14 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_8Y16
Organism: Homo sapiens (Human)
Disease: Microcornea
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 01010504, RRID:CVCL_8Y16 Copy
https://web.expasy.org/cellosaurus/CVCL_L537
Organism: Mus musculus (Mouse)
Category: Hybridoma
Proper citation: ECACC Cat# 89072609, RRID:CVCL_L537 Copy
Misidentified
https://web.expasy.org/cellosaurus/CVCL_3742
Organism: Mus musculus (Mouse)
Category: Spontaneously immortalized cell line
Comments: Virology: Not susceptible to infection by SARS coronavirus 2 (SARS-CoV-2) (COVID-19) (PubMed=33389257)., Problematic cell line: Misidentified. Originally thought to be of human origin but found to be a mouse NCTC clone 929 derivative (PubMed=6451928; PubMed=20143388). Were thought to originate from the synovial fluid in the knee joint of a patient suffering from degenerative arthritis..
Proper citation: ECACC Cat# 90010305, RRID:CVCL_3742 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_0358
Organism: Mus musculus (Mouse)
Disease: Mouse reticulum cell sarcoma
Category: Cancer cell line
Comments: Part of: Tumor Immunology Bank (TIB) collection from Salk (transferred to ATCC in 1981).
Proper citation: ECACC Cat# 91051511, RRID:CVCL_0358 Copy
https://web.expasy.org/cellosaurus/CVCL_E715
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: 10th International Histocompatibility Workshop (10IHW) cell line panel.
Proper citation: ECACC Cat# 88052035, RRID:CVCL_E715 Copy
https://web.expasy.org/cellosaurus/CVCL_E714
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Jewish; Ashkenazi., Part of: 12th International Histocompatibility Workshop (12IHW) cell line panel.
Proper citation: ECACC Cat# 94022531, RRID:CVCL_E714 Copy
https://web.expasy.org/cellosaurus/CVCL_3531
Organism: Rattus norvegicus (Rat)
Disease: Rat sarcoma
Category: Cancer cell line
Comments: Characteristics: Used in studies of amino acid requirements and L-asparagine metabolism (IZSLER=BS TCL 31).
Proper citation: ECACC Cat# 90111913, RRID:CVCL_3531 Copy
https://web.expasy.org/cellosaurus/CVCL_E717
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian; English., Part of: 10th International Histocompatibility Workshop (10IHW) cell line panel.
Proper citation: ECACC Cat# 88052030, RRID:CVCL_E717 Copy
https://web.expasy.org/cellosaurus/CVCL_8X81
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,fra(X)(q27) (ECACC=92012307)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92012307, RRID:CVCL_8X81 Copy
https://web.expasy.org/cellosaurus/CVCL_8X79
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,fra(X)(q27) (ECACC=92012304)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92012304, RRID:CVCL_8X79 Copy
https://web.expasy.org/cellosaurus/CVCL_8X77
Organism: Homo sapiens (Human)
Disease: Seckel syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,Y,r(X)(p22.3;q28) (ECACC=91102601)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 91102601, RRID:CVCL_8X77 Copy
https://web.expasy.org/cellosaurus/CVCL_8X72
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,fra(X)(q27) (ECACC=90091401)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90091401, RRID:CVCL_8X72 Copy
https://web.expasy.org/cellosaurus/CVCL_8X73
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,fra(X)(q27.3) 10% in 70 metaphases (ECACC=91071906)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 91071906, RRID:CVCL_8X73 Copy
https://web.expasy.org/cellosaurus/CVCL_8X82
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,fra(X)(q27.3) (ECACC=92020605)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92020605, RRID:CVCL_8X82 Copy
https://web.expasy.org/cellosaurus/CVCL_8X88
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,+fra(X) (ECACC=92080611)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 92080611, RRID:CVCL_8X88 Copy
https://web.expasy.org/cellosaurus/CVCL_8X76
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 91091106, RRID:CVCL_8X76 Copy
https://web.expasy.org/cellosaurus/CVCL_8X74
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,fra(X)(q27) (ECACC=91080806)., Population: Caucasian., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 91080806, RRID:CVCL_8X74 Copy
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