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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_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: RRID:CVCL_0P92 Copy
https://web.expasy.org/cellosaurus/CVCL_F657
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM01416, RRID:CVCL_F657 Copy
https://web.expasy.org/cellosaurus/CVCL_AV86
Organism: Homo sapiens (Human)
Disease: Hereditary orotic aciduria
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_AV86 Copy
https://web.expasy.org/cellosaurus/CVCL_J115
Organism: Homo sapiens (Human)
Disease: Hepatocyte nuclear factor 4-alpha associated monogenic diabetes
Category: Finite cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.
Proper citation: RRID:CVCL_J115 Copy
https://web.expasy.org/cellosaurus/CVCL_D872
Organism: Homo sapiens (Human)
Disease: Maple syrup urine disease
Category: Transformed cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_D872 Copy
https://web.expasy.org/cellosaurus/CVCL_0M10
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Jewish; Ashkenazi.
Proper citation: RRID:CVCL_0M10 Copy
https://web.expasy.org/cellosaurus/CVCL_X246
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,X,der(9)t(X;9)(q34;q12) (PubMed=10377420)., Population: African American.
Proper citation: Coriell Cat# GM01414, RRID:CVCL_X246 Copy
https://web.expasy.org/cellosaurus/CVCL_1Y25
Organism: Homo sapiens (Human)
Disease: Galactosemia
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_1Y25 Copy
https://web.expasy.org/cellosaurus/CVCL_V830
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(1;7)(1qter->1p34::7p13->7pter;7qter->7p13::1p34->1pter) (Coriell=GM01356)., Population: Caucasian.
Proper citation: RRID:CVCL_V830 Copy
https://web.expasy.org/cellosaurus/CVCL_2H13
Organism: Homo sapiens (Human)
Disease: Homocystinuria
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_2H13 Copy
https://web.expasy.org/cellosaurus/CVCL_X251
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_X251 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JD84
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM01534, RRID:CVCL_JD84 Copy
https://web.expasy.org/cellosaurus/CVCL_M986
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(5;12)(5pter->5q33::12q24->12qter;12pter->12q24::5q33->5qter) (Coriell=GM01536)., Population: African American., Part of: Human variation panel.
Proper citation: RRID:CVCL_M986 Copy
https://web.expasy.org/cellosaurus/CVCL_X250
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: African American.
Proper citation: Coriell Cat# GM01535, RRID:CVCL_X250 Copy
https://web.expasy.org/cellosaurus/CVCL_2H22
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM01558, RRID:CVCL_2H22 Copy
https://web.expasy.org/cellosaurus/CVCL_EJ27
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_EJ27 Copy
https://web.expasy.org/cellosaurus/CVCL_AA15
Organism: Homo sapiens (Human)
Disease: Familial dysautonomia
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM01465, RRID:CVCL_AA15 Copy
https://web.expasy.org/cellosaurus/CVCL_V808
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,t(4;11)(4pter->4q23::11q11->11qter;11pter->11q11::4q23->4qter) [8]; 45,X,t(4;11)(4pter->4q23::11q11->11qter;11pter->11q11::4q23->4qter),add(19)(?::p13.3->qter) [2] (Coriell=GM01561)., Population: Caucasian.
Proper citation: Coriell Cat# GM01561, RRID:CVCL_V808 Copy
https://web.expasy.org/cellosaurus/CVCL_4N14
Organism: Homo sapiens (Human)
Disease: Hyperlipoproteinemia, type IIa
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_4N14 Copy
https://web.expasy.org/cellosaurus/CVCL_AI29
Organism: Homo sapiens (Human)
Disease: Hepatocyte nuclear factor 4-alpha associated monogenic diabetes
Category: Transformed cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.
Proper citation: RRID:CVCL_AI29 Copy
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