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_AM51
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.
Proper citation: Coriell Cat# GM10536, RRID:CVCL_AM51 Copy
https://web.expasy.org/cellosaurus/CVCL_AM40
Organism: Homo sapiens (Human)
Disease: Retinitis pigmentosa
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.
Proper citation: Coriell Cat# GM10524, RRID:CVCL_AM40 Copy
https://web.expasy.org/cellosaurus/CVCL_AM51
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.
Proper citation: RRID:CVCL_AM51 Copy
https://web.expasy.org/cellosaurus/CVCL_0Q13
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_0Q13 Copy
https://web.expasy.org/cellosaurus/CVCL_N150
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Pacific., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel.
Proper citation: RRID:CVCL_N150 Copy
https://web.expasy.org/cellosaurus/CVCL_2T87
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(20;21)(20pter->20q11.2::21p11.2->21pter;21qter->21p11.2::20q11.2->20qter) (Coriell=GM10613).
Proper citation: Coriell Cat# GM10613, RRID:CVCL_2T87 Copy
https://web.expasy.org/cellosaurus/CVCL_AM48
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.
Proper citation: Coriell Cat# GM10533, RRID:CVCL_AM48 Copy
https://web.expasy.org/cellosaurus/CVCL_5P18
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_5P18 Copy
https://web.expasy.org/cellosaurus/CVCL_0Q13
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM10566, RRID:CVCL_0Q13 Copy
https://web.expasy.org/cellosaurus/CVCL_0R05
Organism: Homo sapiens (Human)
Disease: Greig syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM10609, RRID:CVCL_0R05 Copy
https://web.expasy.org/cellosaurus/CVCL_0Q14
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_0Q14 Copy
https://web.expasy.org/cellosaurus/CVCL_DA32
Organism: Homo sapiens (Human)
Disease: Neuronal ceroid lipofuscinosis type 2
Category: Finite cell line
Comments: Population: Asian.
Proper citation: Coriell Cat# GM10570, RRID:CVCL_DA32 Copy
https://web.expasy.org/cellosaurus/CVCL_AM48
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.
Proper citation: RRID:CVCL_AM48 Copy
https://web.expasy.org/cellosaurus/CVCL_N149
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Pacific., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel.
Proper citation: Coriell Cat# GM10542, RRID:CVCL_N149 Copy
https://web.expasy.org/cellosaurus/CVCL_AM49
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.
Proper citation: Coriell Cat# GM10534, RRID:CVCL_AM49 Copy
https://web.expasy.org/cellosaurus/CVCL_AM40
Organism: Homo sapiens (Human)
Disease: Retinitis pigmentosa
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection.
Proper citation: RRID:CVCL_AM40 Copy
https://web.expasy.org/cellosaurus/CVCL_0Q19
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_0Q19 Copy
https://web.expasy.org/cellosaurus/CVCL_AT11
Organism: Homo sapiens (Human)
Disease: Glutaric acidemia type 1
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_AT11 Copy
https://web.expasy.org/cellosaurus/CVCL_4I29
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection.
Proper citation: Coriell Cat# GM10703, RRID:CVCL_4I29 Copy
https://web.expasy.org/cellosaurus/CVCL_W906
Organism: Homo sapiens (Human)
Disease: Hereditary hemorrhagic telangiectasia
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_W906 Copy
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