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_JE12
Organism: Homo sapiens (Human)
Disease: WAGR syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_JE12 Copy
https://web.expasy.org/cellosaurus/CVCL_7654
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: African American., Part of: Human variation panel.
Proper citation: Coriell Cat# GM03725, RRID:CVCL_7654 Copy
https://web.expasy.org/cellosaurus/CVCL_1N78
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XY,t(1;20)(1qter->1p13::20q13.3->20qter;20pter->20q13.3::1p13->1pter) (Coriell=GM03876)., Population: Caucasian.
Proper citation: RRID:CVCL_1N78 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_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_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_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_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_9Z41
Organism: Homo sapiens (Human)
Disease: Refsum disease
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03896, RRID:CVCL_9Z41 Copy
https://web.expasy.org/cellosaurus/CVCL_1K35
Organism: Homo sapiens (Human)
Disease: Roberts-SC phocomelia syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XY [46%]; 47,XY,+7 [54%] (Coriell=GM03913)., Population: Caucasian; French Canadian.
Proper citation: Coriell Cat# GM03913, RRID:CVCL_1K35 Copy
https://web.expasy.org/cellosaurus/CVCL_EF95
Organism: Homo sapiens (Human)
Disease: Glutathione synthetase deficiency
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_EF95 Copy
https://web.expasy.org/cellosaurus/CVCL_9Z42
Organism: Homo sapiens (Human)
Disease: Refsum disease
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03897, RRID:CVCL_9Z42 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: RRID:CVCL_W306 Copy
https://web.expasy.org/cellosaurus/CVCL_DD76
Organism: Homo sapiens (Human)
Disease: Hereditary optic atrophy
Category: Finite cell line
Comments: Population: Jewish.
Proper citation: RRID:CVCL_DD76 Copy
https://web.expasy.org/cellosaurus/CVCL_X114
Organism: Homo sapiens (Human)
Disease: Cri du chat syndrome
Category: Finite cell line
Proper citation: Coriell Cat# GM03912, RRID:CVCL_X114 Copy
https://web.expasy.org/cellosaurus/CVCL_AK90
Organism: Homo sapiens (Human)
Disease: Retinitis pigmentosa
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03893, RRID:CVCL_AK90 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: RRID:CVCL_W305 Copy
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