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.
Discontinued
https://web.expasy.org/cellosaurus/CVCL_L968
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM02205, RRID:CVCL_L968 Copy
https://web.expasy.org/cellosaurus/CVCL_DD69
Organism: Homo sapiens (Human)
Disease: Osteogenesis imperfecta
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_DD69 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JB67
Organism: Homo sapiens (Human)
Disease: Wolman disease
Category: Finite cell line
Proper citation: Coriell Cat# GM02211, RRID:CVCL_JB67 Copy
https://web.expasy.org/cellosaurus/CVCL_L487
Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line
Proper citation: RRID:CVCL_L487 Copy
https://web.expasy.org/cellosaurus/CVCL_H179
Organism: Homo sapiens (Human)
Disease: Metachromatic leukodystrophy
Category: Finite cell line
Comments: Donor information: At sampling donor was not affected with metachromatic leukodystrophy but at risk for disease., Population: Caucasian.
Proper citation: RRID:CVCL_H179 Copy
https://web.expasy.org/cellosaurus/CVCL_7356
Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM02290, RRID:CVCL_7356 Copy
https://web.expasy.org/cellosaurus/CVCL_4N23
Organism: Homo sapiens (Human)
Disease: Autosomal recessive torsion dystonia 2
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM02306, RRID:CVCL_4N23 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JD75
Organism: Homo sapiens (Human)
Disease: Fanconi anemia
Category: Finite cell line
Proper citation: Coriell Cat# GM02364, RRID:CVCL_JD75 Copy
https://web.expasy.org/cellosaurus/CVCL_D869
Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM02338, RRID:CVCL_D869 Copy
https://web.expasy.org/cellosaurus/CVCL_AK22
Organism: Homo sapiens (Human)
Disease: Fanconi anemia, complementation group G
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_AK22 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_U388
Organism: Homo sapiens (Human)
Disease: Tay-Sachs disease
Category: Transformed cell line
Proper citation: RRID:CVCL_U388 Copy
https://web.expasy.org/cellosaurus/CVCL_AA18
Organism: Homo sapiens (Human)
Disease: Familial dysautonomia
Category: Finite cell line
Comments: Population: Jewish; Ashkenazi.
Proper citation: RRID:CVCL_AA18 Copy
https://web.expasy.org/cellosaurus/CVCL_4J51
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM02336, RRID:CVCL_4J51 Copy
https://web.expasy.org/cellosaurus/CVCL_L488
Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_L488 Copy
https://web.expasy.org/cellosaurus/CVCL_4N25
Organism: Homo sapiens (Human)
Disease: Hyperlipoproteinemia, type IIa
Category: Transformed cell line
Proper citation: Coriell Cat# GM02373, RRID:CVCL_4N25 Copy
https://web.expasy.org/cellosaurus/CVCL_X091
Organism: Homo sapiens (Human)
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: Coriell Cat# GM02346, RRID:CVCL_X091 Copy
https://web.expasy.org/cellosaurus/CVCL_5L46
Organism: Homo sapiens (Human)
Disease: Tuberous sclerosis 1
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_5L46 Copy
https://web.expasy.org/cellosaurus/CVCL_5L45
Organism: Homo sapiens (Human)
Disease: Tuberous sclerosis 1
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM02332, RRID:CVCL_5L45 Copy
https://web.expasy.org/cellosaurus/CVCL_5L45
Organism: Homo sapiens (Human)
Disease: Tuberous sclerosis 1
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_5L45 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_L972
Organism: Homo sapiens (Human)
Disease: Galactosemia
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_L972 Copy
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