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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_CX10
Organism: Homo sapiens (Human)
Disease: Glycine encephalopathy
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM01302, RRID:CVCL_CX10 Copy
https://web.expasy.org/cellosaurus/CVCL_HQ02
Organism: Homo sapiens (Human)
Disease: Congenital contractural arachnodactyly
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM01352, RRID:CVCL_HQ02 Copy
https://web.expasy.org/cellosaurus/CVCL_V532
Organism: Homo sapiens (Human)
Disease: Hurler syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM01257, RRID:CVCL_V532 Copy
https://web.expasy.org/cellosaurus/CVCL_V802
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: African American.
Proper citation: Coriell Cat# GM01252, RRID:CVCL_V802 Copy
https://web.expasy.org/cellosaurus/CVCL_4D81
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,ins(5;6)(5pter->5q33::6q15->6q25::5q33->5qter;6pter->6q15::6q25->6qter) (Coriell=GM01222)., Population: African American.
Proper citation: Coriell Cat# GM01222, RRID:CVCL_4D81 Copy
https://web.expasy.org/cellosaurus/CVCL_V801
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM01224, RRID:CVCL_V801 Copy
https://web.expasy.org/cellosaurus/CVCL_W636
Organism: Homo sapiens (Human)
Disease: 47,XYY syndrome
Category: Finite cell line
Comments: Karyotypic information: 47,XYY (Coriell=GM01250)., Population: African American.
Proper citation: Coriell Cat# GM01250, RRID:CVCL_W636 Copy
https://web.expasy.org/cellosaurus/CVCL_0P90
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,t(1;2)(1qter->1p36::2q31->2qter;2pter->2q31::1p36->1pter) (Coriell=GM01230)., Population: Cuban.
Proper citation: Coriell Cat# GM01230, RRID:CVCL_0P90 Copy
https://web.expasy.org/cellosaurus/CVCL_M985
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: African American., Part of: Human variation panel.
Proper citation: Coriell Cat# GM01251, RRID:CVCL_M985 Copy
https://web.expasy.org/cellosaurus/CVCL_JC90
Organism: Homo sapiens (Human)
Disease: Androgen insensitivity syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XY; but phenotypically female (Coriell=GM01404)., Population: African American.
Proper citation: Coriell Cat# GM01404, RRID:CVCL_JC90 Copy
https://web.expasy.org/cellosaurus/CVCL_0P92
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;21)(q11;p11) (PubMed=10377420)., Population: African American.
Proper citation: Coriell Cat# GM01411, RRID:CVCL_0P92 Copy
https://web.expasy.org/cellosaurus/CVCL_2H16
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM01446, RRID:CVCL_2H16 Copy
https://web.expasy.org/cellosaurus/CVCL_1V15
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM01393, RRID:CVCL_1V15 Copy
https://web.expasy.org/cellosaurus/CVCL_7319
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM01381, RRID:CVCL_7319 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_DF17
Organism: Homo sapiens (Human)
Disease: Retinoblastoma
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM01408, RRID:CVCL_DF17 Copy
https://web.expasy.org/cellosaurus/CVCL_J114
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,+der(9)(9pter->9q21.2::13q12.1->13qter)mat,-13 (Coriell=GM01387)., Population: Caucasian.
Proper citation: Coriell Cat# GM01387, RRID:CVCL_J114 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JD99
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM01420, RRID:CVCL_JD99 Copy
https://web.expasy.org/cellosaurus/CVCL_0M11
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM01444, RRID:CVCL_0M11 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_DF17
Organism: Homo sapiens (Human)
Disease: Retinoblastoma
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# AG01408, RRID:CVCL_DF17 Copy
https://web.expasy.org/cellosaurus/CVCL_2H17
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM01447, RRID:CVCL_2H17 Copy
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