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_2Z70
Organism: Homo sapiens (Human)
Disease: Nevoid basal cell carcinoma syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_2Z70 Copy
https://web.expasy.org/cellosaurus/CVCL_R905
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_R905 Copy
https://web.expasy.org/cellosaurus/CVCL_V426
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_V426 Copy
https://web.expasy.org/cellosaurus/CVCL_0Q03
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(2;10)(2qter->2p23::10q26->10qter;10pter->10q26::2p23->2pter) (Coriell=GM01683)., Population: Caucasian.
Proper citation: Coriell Cat# GM01683, RRID:CVCL_0Q03 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JB62
Organism: Homo sapiens (Human)
Disease: Niemann-Pick disease, type B
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_JB62 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JB62
Organism: Homo sapiens (Human)
Disease: Niemann-Pick disease, type B
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM01669, RRID:CVCL_JB62 Copy
https://web.expasy.org/cellosaurus/CVCL_V811
Organism: Homo sapiens (Human)
Disease: Duchenne muscular dystrophy
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;11)(p21;q13) (PubMed=10377420)., Population: Caucasian.
Proper citation: RRID:CVCL_V811 Copy
https://web.expasy.org/cellosaurus/CVCL_JC91
Organism: Homo sapiens (Human)
Disease: Androgen insensitivity syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_JC91 Copy
https://web.expasy.org/cellosaurus/CVCL_1Y29
Organism: Homo sapiens (Human)
Disease: Galactosemia
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_1Y29 Copy
https://web.expasy.org/cellosaurus/CVCL_7333
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM01681, RRID:CVCL_7333 Copy
https://web.expasy.org/cellosaurus/CVCL_0Q03
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(2;10)(2qter->2p23::10q26->10qter;10pter->10q26::2p23->2pter) (Coriell=GM01683)., Population: Caucasian.
Proper citation: RRID:CVCL_0Q03 Copy
https://web.expasy.org/cellosaurus/CVCL_U387
Organism: Homo sapiens (Human)
Disease: GM2-gangliosidosis, AB variant
Category: Finite cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_U387 Copy
https://web.expasy.org/cellosaurus/CVCL_1D19
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;7)(q21;p22) (PubMed=10377420)., Population: Caucasian.
Proper citation: RRID:CVCL_1D19 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JC92
Organism: Homo sapiens (Human)
Disease: Ataxia telangiectasia syndrome
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM01740, RRID:CVCL_JC92 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_X254
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_X254 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JC84
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM01824, RRID:CVCL_JC84 Copy
https://web.expasy.org/cellosaurus/CVCL_9R67
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_9R67 Copy
https://web.expasy.org/cellosaurus/CVCL_AM87
Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome, type II
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_AM87 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_7339
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# GM17215, RRID:CVCL_7339 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_L963
Organism: Homo sapiens (Human)
Disease: Hyperlipoproteinemia, type IIa
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_L963 Copy
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