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_GS55
Organism: Homo sapiens (Human)
Disease: Adenosine deaminase deficiency
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_GS55 Copy
https://web.expasy.org/cellosaurus/CVCL_L945
Organism: Homo sapiens (Human)
Disease: Familial adenomatous polyposis
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM02355, RRID:CVCL_L945 Copy
https://web.expasy.org/cellosaurus/CVCL_GR98
Organism: Homo sapiens (Human)
Disease: Type 1 diabetes mellitus
Category: Finite cell line
Comments: Population: Native Central American; Pima.
Proper citation: Coriell Cat# GM02442, RRID:CVCL_GR98 Copy
https://web.expasy.org/cellosaurus/CVCL_AK24
Organism: Homo sapiens (Human)
Disease: Fanconi anemia, complementation group A
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM02363, RRID:CVCL_AK24 Copy
https://web.expasy.org/cellosaurus/CVCL_AK23
Organism: Homo sapiens (Human)
Disease: Fanconi anemia, complementation group A
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_AK23 Copy
https://web.expasy.org/cellosaurus/CVCL_VE86
Organism: Homo sapiens (Human)
Disease: GM1 gangliosidosis
Category: Induced pluripotent stem cell
Comments: Population: Turkish.
Proper citation: RRID:CVCL_VE86 Copy
https://web.expasy.org/cellosaurus/CVCL_W149
Organism: Homo sapiens (Human)
Disease: GM1 gangliosidosis
Category: Finite cell line
Comments: Population: Turkish., From: Montreal Children's Hospital cell repository; Montreal; Canada.
Proper citation: RRID:CVCL_W149 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_L975
Organism: Homo sapiens (Human)
Disease: Chediak-Higashi syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_L975 Copy
https://web.expasy.org/cellosaurus/CVCL_H181
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM02380, RRID:CVCL_H181 Copy
https://web.expasy.org/cellosaurus/CVCL_1R62
Organism: Homo sapiens (Human)
Disease: Coffin-Lowry syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM02365, RRID:CVCL_1R62 Copy
https://web.expasy.org/cellosaurus/CVCL_9R69
Organism: Homo sapiens (Human)
Disease: Mucolipidosis type IIIA
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_9R69 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_UY61
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_UY61 Copy
https://web.expasy.org/cellosaurus/CVCL_H183
Organism: Homo sapiens (Human)
Disease: Trisomy 18
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_H183 Copy
https://web.expasy.org/cellosaurus/CVCL_X091
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,t(4;16)(4pter->4q35::16q22.1->16qter;16pter->16q22.1::4q35->4qter) (Coriell=GM02346)., Population: Caucasian.
Proper citation: RRID:CVCL_X091 Copy
https://web.expasy.org/cellosaurus/CVCL_M997
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# GM17252, RRID:CVCL_M997 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JD75
Organism: Homo sapiens (Human)
Disease: Fanconi anemia
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_JD75 Copy
https://web.expasy.org/cellosaurus/CVCL_B5QU
Organism: Homo sapiens (Human)
Disease: Sickle cell disease
Category: Induced pluripotent stem cell
Comments:
Proper citation: RRID:CVCL_B5QU Copy
https://web.expasy.org/cellosaurus/CVCL_GS56
Organism: Homo sapiens (Human)
Disease: Adenosine deaminase deficiency
Category: Finite cell line
Comments: Population: Caucasian; Swiss.
Proper citation: RRID:CVCL_GS56 Copy
https://web.expasy.org/cellosaurus/CVCL_M996
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_M996 Copy
https://web.expasy.org/cellosaurus/CVCL_5M73
Organism: Homo sapiens (Human)
Disease: Dyggve-Melchior-Clausen syndrome
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM02437, RRID:CVCL_5M73 Copy
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