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_AK94
Organism: Homo sapiens (Human)
Disease: Retinitis pigmentosa
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03910, RRID:CVCL_AK94 Copy
https://web.expasy.org/cellosaurus/CVCL_1H75
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_1H75 Copy
https://web.expasy.org/cellosaurus/CVCL_1H68
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_1H68 Copy
https://web.expasy.org/cellosaurus/CVCL_W304
Organism: Homo sapiens (Human)
Disease: Usher syndrome type 1
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_W304 Copy
https://web.expasy.org/cellosaurus/CVCL_AK87
Organism: Homo sapiens (Human)
Disease: Retinitis pigmentosa
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03836, RRID:CVCL_AK87 Copy
https://web.expasy.org/cellosaurus/CVCL_W303
Organism: Homo sapiens (Human)
Disease: Usher syndrome type 1
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03889, RRID:CVCL_W303 Copy
https://web.expasy.org/cellosaurus/CVCL_1H71
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Finite cell line
Comments: Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian.
Proper citation: Coriell Cat# GM03866, RRID:CVCL_1H71 Copy
https://web.expasy.org/cellosaurus/CVCL_1H74
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03869, RRID:CVCL_1H74 Copy
https://web.expasy.org/cellosaurus/CVCL_AM66
Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03850, RRID:CVCL_AM66 Copy
https://web.expasy.org/cellosaurus/CVCL_W305
Organism: Homo sapiens (Human)
Disease: Usher syndrome type 1
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03891, RRID:CVCL_W305 Copy
https://web.expasy.org/cellosaurus/CVCL_2S97
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(3;10)(3pter->3q25::10p15->10pter;10qter->10p15::3q25->3qter) (Coriell=GM03882)., Population: Caucasian.
Proper citation: RRID:CVCL_2S97 Copy
https://web.expasy.org/cellosaurus/CVCL_AK91
Organism: Homo sapiens (Human)
Disease: Retinitis pigmentosa
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03894, RRID:CVCL_AK91 Copy
https://web.expasy.org/cellosaurus/CVCL_1H66
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03861, RRID:CVCL_1H66 Copy
https://web.expasy.org/cellosaurus/CVCL_2S96
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(11;22)(11pter->11q23::22q11.2->22qter;22pter->22q11.2::11q23->11qter)mat (Coriell=GM03847)., Population: Caucasian.
Proper citation: Coriell Cat# GM03847, RRID:CVCL_2S96 Copy
https://web.expasy.org/cellosaurus/CVCL_1H70
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_1H70 Copy
https://web.expasy.org/cellosaurus/CVCL_W306
Organism: Homo sapiens (Human)
Disease: Usher syndrome type 1
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03892, RRID:CVCL_W306 Copy
https://web.expasy.org/cellosaurus/CVCL_W303
Organism: Homo sapiens (Human)
Disease: Usher syndrome type 1
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_W303 Copy
https://web.expasy.org/cellosaurus/CVCL_EF94
Organism: Homo sapiens (Human)
Disease: Glutathione synthetase deficiency
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_EF94 Copy
https://web.expasy.org/cellosaurus/CVCL_W307
Organism: Homo sapiens (Human)
Disease: Usher syndrome type 1
Category: Transformed cell line
Comments: Population: Caucasian; German.
Proper citation: RRID:CVCL_W307 Copy
https://web.expasy.org/cellosaurus/CVCL_GY19
Organism: Homo sapiens (Human)
Disease: Leber congenital amaurosis
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_GY19 Copy
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