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.
https://web.expasy.org/cellosaurus/CVCL_N082
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples.
Proper citation: Coriell Cat# GM08428, RRID:CVCL_N082 Copy
https://web.expasy.org/cellosaurus/CVCL_DS19
Organism: Homo sapiens (Human)
Disease: Sialic acid storage disease
Category: Finite cell line
Comments: Population: Caucasian; Finnish.
Proper citation: RRID:CVCL_DS19 Copy
https://web.expasy.org/cellosaurus/CVCL_N083
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples.
Proper citation: RRID:CVCL_N083 Copy
https://web.expasy.org/cellosaurus/CVCL_7484
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_7484 Copy
https://web.expasy.org/cellosaurus/CVCL_IN22
Organism: Homo sapiens (Human)
Disease: Neuropathy, hereditary sensory and autonomic, type IV
Category: Transformed cell line
Comments: Population: Ecuadorian.
Proper citation: RRID:CVCL_IN22 Copy
https://web.expasy.org/cellosaurus/CVCL_DD82
Organism: Homo sapiens (Human)
Disease: Osteogenesis imperfecta type II
Category: Finite cell line
Comments: Population: Caucasian; Swiss.
Proper citation: RRID:CVCL_DD82 Copy
https://web.expasy.org/cellosaurus/CVCL_2Y92
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; Amish.
Proper citation: Coriell Cat# GM08663, RRID:CVCL_2Y92 Copy
https://web.expasy.org/cellosaurus/CVCL_5N89
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM08778, RRID:CVCL_5N89 Copy
https://web.expasy.org/cellosaurus/CVCL_DF29
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; English.
Proper citation: RRID:CVCL_DF29 Copy
https://web.expasy.org/cellosaurus/CVCL_9S91
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 47,XY,+i(18)(pter->p10:p10->pter) (Coriell=GM08681)., Population: Caucasian.
Proper citation: RRID:CVCL_9S91 Copy
https://web.expasy.org/cellosaurus/CVCL_1K60
Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type VII
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM08683, RRID:CVCL_1K60 Copy
https://web.expasy.org/cellosaurus/CVCL_2Y89
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; Amish.
Proper citation: RRID:CVCL_2Y89 Copy
https://web.expasy.org/cellosaurus/CVCL_W728
Organism: Homo sapiens (Human)
Disease: Zellweger syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM08764, RRID:CVCL_W728 Copy
https://web.expasy.org/cellosaurus/CVCL_E129
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_E129 Copy
https://web.expasy.org/cellosaurus/CVCL_5N85
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM08618, RRID:CVCL_5N85 Copy
https://web.expasy.org/cellosaurus/CVCL_2T57
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_2T57 Copy
https://web.expasy.org/cellosaurus/CVCL_EJ56
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM08697, RRID:CVCL_EJ56 Copy
https://web.expasy.org/cellosaurus/CVCL_EH04
Organism: Homo sapiens (Human)
Disease: Congenital adrenal gland hypoplasia
Category: Finite cell line
Comments: Population: African American.
Proper citation: Coriell Cat# GM08788, RRID:CVCL_EH04 Copy
https://web.expasy.org/cellosaurus/CVCL_N086
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples.
Proper citation: RRID:CVCL_N086 Copy
https://web.expasy.org/cellosaurus/CVCL_DF30
Organism: Homo sapiens (Human)
Disease: Retinoblastoma
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM08776, RRID:CVCL_DF30 Copy
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