Searching the RRID Resource Information Network
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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.
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_5P51
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM11403, RRID:CVCL_5P51 Copy
https://web.expasy.org/cellosaurus/CVCL_4F64
Organism: Homo sapiens (Human)
Disease: Very long-chain acyl-CoA dehydrogenase deficiency
Category: Finite cell line
Comments: Population: Asian.
Proper citation: Coriell Cat# GM11408, RRID:CVCL_4F64 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_5P51
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_5P51 Copy
https://web.expasy.org/cellosaurus/CVCL_H552
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_H552 Copy
https://web.expasy.org/cellosaurus/CVCL_5P48
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5P48 Copy
https://web.expasy.org/cellosaurus/CVCL_9X19
Organism: Homo sapiens (Human)
Disease: Rhizomelic chondrodysplasia punctata
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM11349, RRID:CVCL_9X19 Copy
https://web.expasy.org/cellosaurus/CVCL_5P45
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM11386, RRID:CVCL_5P45 Copy
https://web.expasy.org/cellosaurus/CVCL_DB80
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; Amish.
Proper citation: RRID:CVCL_DB80 Copy
https://web.expasy.org/cellosaurus/CVCL_4E06
Organism: Homo sapiens (Human)
Disease: Ring chromosome 21 syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XX dic,r(21) [36]; 45,XX,-21 [10]; 46,XX,r(21) [4] (Coriell=GM11338)., Population: Caucasian.
Proper citation: RRID:CVCL_4E06 Copy
https://web.expasy.org/cellosaurus/CVCL_2U06
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 45,XY,der(14)(14qter->14p12::18q11->18qter),-18 (Coriell=GM11346)., Population: Caucasian.
Proper citation: Coriell Cat# GM11346, RRID:CVCL_2U06 Copy
https://web.expasy.org/cellosaurus/CVCL_9R93
Organism: Homo sapiens (Human)
Disease: Weaver syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM11407, RRID:CVCL_9R93 Copy
https://web.expasy.org/cellosaurus/CVCL_2U07
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(8;10)(8qter->8p11.2::10q24->10qter;10pter->10q24::8p11.2->8pter) (Coriell=GM11397).
Proper citation: Coriell Cat# GM11397, RRID:CVCL_2U07 Copy
https://web.expasy.org/cellosaurus/CVCL_U533
Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM11388, RRID:CVCL_U533 Copy
https://web.expasy.org/cellosaurus/CVCL_9X19
Organism: Homo sapiens (Human)
Disease: Rhizomelic chondrodysplasia punctata
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_9X19 Copy
https://web.expasy.org/cellosaurus/CVCL_AJ50
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_AJ50 Copy
https://web.expasy.org/cellosaurus/CVCL_AJ49
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_AJ49 Copy
https://web.expasy.org/cellosaurus/CVCL_9X17
Organism: Homo sapiens (Human)
Disease: Rhizomelic chondrodysplasia punctata
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM11347, RRID:CVCL_9X17 Copy
https://web.expasy.org/cellosaurus/CVCL_4F64
Organism: Homo sapiens (Human)
Disease: Very long-chain acyl-CoA dehydrogenase deficiency
Category: Finite cell line
Comments: Population: Asian.
Proper citation: RRID:CVCL_4F64 Copy
https://web.expasy.org/cellosaurus/CVCL_5P47
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM11389, RRID:CVCL_5P47 Copy
https://web.expasy.org/cellosaurus/CVCL_N182
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 49,XYYYY (Coriell=GM11419)., Population: Indian (from Guyana)., Part of: Human variation panel.
Proper citation: RRID:CVCL_N182 Copy
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