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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_1V15
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_1V15 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_X080
Organism: Homo sapiens (Human)
Disease: Trisomy 18
Category: Finite cell line
Comments: Karyotypic information: 47,XY,+18.arr(18)x3 (Coriell=GM01359)., Population: Caucasian.
Proper citation: RRID:CVCL_X080 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JB82
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM01358, RRID:CVCL_JB82 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
https://web.expasy.org/cellosaurus/CVCL_H974
Organism: Homo sapiens (Human)
Disease: Porphyria cutanea tarda
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM01482, RRID:CVCL_H974 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_V214
Organism: Homo sapiens (Human)
Disease: Cystic fibrosis
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_V214 Copy
https://web.expasy.org/cellosaurus/CVCL_2H21
Organism: Homo sapiens (Human)
Disease: Homocystinuria
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_2H21 Copy
https://web.expasy.org/cellosaurus/CVCL_V809
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 6,XY,rec(13)(pter->q22::p11->pter)pat (Coriell=GM01570).
Proper citation: RRID:CVCL_V809 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_X081
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM01549, RRID:CVCL_X081 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_4N17
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,rec(3)(qter->p25::q21->qter) [46]; 46,XY,rec(3)(qter->p25::q21->qter),+8 [4] (Coriell=GM01506).
Proper citation: Coriell Cat# GM01506, RRID:CVCL_4N17 Copy
https://web.expasy.org/cellosaurus/CVCL_X249
Organism: Homo sapiens (Human)
Disease: Developmental delay
Category: Finite cell line
Comments: Karyotypic information: 46,XY,der(5)(5pter->5q33::6q15->6q25::5q33->5qter)mat (Coriell=GM01524)., Population: African American.
Proper citation: RRID:CVCL_X249 Copy
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