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_1I04
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM04217, RRID:CVCL_1I04 Copy
https://web.expasy.org/cellosaurus/CVCL_1I07
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian.
Proper citation: RRID:CVCL_1I07 Copy
https://web.expasy.org/cellosaurus/CVCL_1I03
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_1I03 Copy
https://web.expasy.org/cellosaurus/CVCL_1H86
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM04191, RRID:CVCL_1H86 Copy
https://web.expasy.org/cellosaurus/CVCL_1H97
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Donor information: At sampling donor was not affected with Huntington disease but at low risk for disease., Population: Caucasian.
Proper citation: Coriell Cat# GM04203, RRID:CVCL_1H97 Copy
https://web.expasy.org/cellosaurus/CVCL_1H88
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_1H88 Copy
https://web.expasy.org/cellosaurus/CVCL_4N43
Organism: Homo sapiens (Human)
Disease: Kearns-Sayre syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_4N43 Copy
https://web.expasy.org/cellosaurus/CVCL_Y868
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Part of: Venezuelan Huntington disease kindreds subcollection.
Proper citation: Coriell Cat# GM04286, RRID:CVCL_Y868 Copy
https://web.expasy.org/cellosaurus/CVCL_F113
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Part of: Venezuelan Huntington disease kindreds subcollection., Part of: Genetic Testing Reference Material (GeT-RM) samples.
Proper citation: RRID:CVCL_F113 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_US61
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Part of: Venezuelan Huntington disease kindreds subcollection.
Proper citation: RRID:CVCL_US61 Copy
https://web.expasy.org/cellosaurus/CVCL_9Y77
Organism: Homo sapiens (Human)
Disease: Albright's hereditary osteodystrophy
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM04411, RRID:CVCL_9Y77 Copy
https://web.expasy.org/cellosaurus/CVCL_4D84
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_4D84 Copy
https://web.expasy.org/cellosaurus/CVCL_5M91
Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_5M91 Copy
https://web.expasy.org/cellosaurus/CVCL_1I18
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Part of: Venezuelan Huntington disease kindreds subcollection.
Proper citation: Coriell Cat# GM04290, RRID:CVCL_1I18 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_US61
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Part of: Venezuelan Huntington disease kindreds subcollection.
Proper citation: Coriell Cat# GM04289, RRID:CVCL_US61 Copy
https://web.expasy.org/cellosaurus/CVCL_Y860
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Part of: Venezuelan Huntington disease kindreds subcollection.
Proper citation: RRID:CVCL_Y860 Copy
https://web.expasy.org/cellosaurus/CVCL_IJ33
Organism: Homo sapiens (Human)
Disease: Galactosialidosis
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_IJ33 Copy
https://web.expasy.org/cellosaurus/CVCL_7408
Organism: Homo sapiens (Human)
Disease: Bloom syndrome
Category: Transformed cell line
Comments: Caution: Coriell has p.Cys1055fs*23 (c.3159delT) (3233delT) as the second mutation for this cell line., Donor information: From Bloom Syndrome Registry patient 87(AlFra) (BSR87)., Population: Caucasian; English and Jewish; Ashkenazi., Part of: Genetic Testing Reference Material (GeT-RM) samples.
Proper citation: RRID:CVCL_7408 Copy
https://web.expasy.org/cellosaurus/CVCL_4D84
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM04347, RRID:CVCL_4D84 Copy
https://web.expasy.org/cellosaurus/CVCL_9Y79
Organism: Homo sapiens (Human)
Disease: Albright's hereditary osteodystrophy
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_9Y79 Copy
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Data set from Kravitz, Owen and Kretizer's 2012 paper "Optogenetic identification of striatal projection neuron subtypes during in vivo recordings."
