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_4N20
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian; Swiss.
Proper citation: RRID:CVCL_4N20 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_7344
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_7344 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JD90
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM01973, RRID:CVCL_JD90 Copy
https://web.expasy.org/cellosaurus/CVCL_0M14
Organism: Homo sapiens (Human)
Disease: Cystic fibrosis
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_0M14 Copy
https://web.expasy.org/cellosaurus/CVCL_W660
Organism: Homo sapiens (Human)
Disease: Hunter syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM01928, RRID:CVCL_W660 Copy
https://web.expasy.org/cellosaurus/CVCL_F591
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_F591 Copy
https://web.expasy.org/cellosaurus/CVCL_X084
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_X084 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_ZP42
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Senescence: Senesces at 22 PDL (PubMed=6492896).
Proper citation: RRID:CVCL_ZP42 Copy
https://web.expasy.org/cellosaurus/CVCL_V467
Organism: Homo sapiens (Human)
Disease: Down syndrome
Category: Finite cell line
Comments: Karyotypic information: 47,XY,+21 [44]; 47,XY,t(1;16)(q21;p13.3],+21 [4]; 46,XY [2] (Coriell=GM02067)., Population: Caucasian.
Proper citation: RRID:CVCL_V467 Copy
https://web.expasy.org/cellosaurus/CVCL_7349
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY [45]; 46,XY,t(4;16)(4qter->4p14::16q24->16qter;16pter->16q24::4p14->4pter) [5] (Coriell=GM02037)., Population: Caucasian.
Proper citation: Coriell Cat# GM02037, RRID:CVCL_7349 Copy
https://web.expasy.org/cellosaurus/CVCL_CZ13
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM02028, RRID:CVCL_CZ13 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_ZP42
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Senescence: Senesces at 22 PDL (PubMed=6492896).
Proper citation: Coriell Cat# GM02060, RRID:CVCL_ZP42 Copy
https://web.expasy.org/cellosaurus/CVCL_H178
Organism: Homo sapiens (Human)
Disease: Metachromatic leukodystrophy
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM02095, RRID:CVCL_H178 Copy
https://web.expasy.org/cellosaurus/CVCL_1H41
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM02079, RRID:CVCL_1H41 Copy
https://web.expasy.org/cellosaurus/CVCL_7350
Organism: Homo sapiens (Human)
Disease: Ataxia telangiectasia syndrome
Category: Finite cell line
Comments: Population: Jewish; Moroccan.
Proper citation: RRID:CVCL_7350 Copy
https://web.expasy.org/cellosaurus/CVCL_X448
Organism: Homo sapiens (Human)
Disease: Aspartylglycosaminuria
Category: Finite cell line
Comments: Population: Caucasian; Finnish.
Proper citation: RRID:CVCL_X448 Copy
https://web.expasy.org/cellosaurus/CVCL_CW97
Organism: Homo sapiens (Human)
Disease: Nephropathic cystinosis
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_CW97 Copy
https://web.expasy.org/cellosaurus/CVCL_9R68
Organism: Homo sapiens (Human)
Disease: Mucolipidosis type IIIA
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_9R68 Copy
https://web.expasy.org/cellosaurus/CVCL_4J44
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_4J44 Copy
https://web.expasy.org/cellosaurus/CVCL_V466
Organism: Homo sapiens (Human)
Disease: Down syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XX,i(21)(qter->q10::q10->qter) [13]; 46,XX [87] (Coriell=GM02058)., Population: Jewish; Ashkenazi.
Proper citation: RRID:CVCL_V466 Copy
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