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_1H59
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# GM02191, RRID:CVCL_1H59 Copy
https://web.expasy.org/cellosaurus/CVCL_4T29
Organism: Homo sapiens (Human)
Disease: Winchester syndrome
Category: Finite cell line
Comments: Population: Puerto Rican.
Proper citation: RRID:CVCL_4T29 Copy
https://web.expasy.org/cellosaurus/CVCL_8A67
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian; Irish.
Proper citation: Coriell Cat# GM02317, RRID:CVCL_8A67 Copy
https://web.expasy.org/cellosaurus/CVCL_W226
Organism: Homo sapiens (Human)
Disease: Hereditary coproporphyria
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_W226 Copy
https://web.expasy.org/cellosaurus/CVCL_4J47
Organism: Homo sapiens (Human)
Disease: Acute intermittent porphyria
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_4J47 Copy
https://web.expasy.org/cellosaurus/CVCL_8A67
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian; Irish.
Proper citation: RRID:CVCL_8A67 Copy
https://web.expasy.org/cellosaurus/CVCL_W662
Organism: Homo sapiens (Human)
Disease: Hunter syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM02268, RRID:CVCL_W662 Copy
https://web.expasy.org/cellosaurus/CVCL_IJ35
Organism: Homo sapiens (Human)
Disease: Galactosialidosis
Category: Finite cell line
Proper citation: Coriell Cat# GM02438, RRID:CVCL_IJ35 Copy
https://web.expasy.org/cellosaurus/CVCL_CZ14
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_CZ14 Copy
https://web.expasy.org/cellosaurus/CVCL_X263
Organism: Homo sapiens (Human)
Disease: Trisomy 9
Category: Finite cell line
Comments: Karyotypic information: 47,XX,+9 [5]; 46,XX [45] (Coriell=GM02329)., Population: Caucasian.
Proper citation: Coriell Cat# GM02329, RRID:CVCL_X263 Copy
https://web.expasy.org/cellosaurus/CVCL_GR98
Organism: Homo sapiens (Human)
Disease: Type 1 diabetes mellitus
Category: Finite cell line
Comments: Population: Native Central American; Pima.
Proper citation: RRID:CVCL_GR98 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_L974
Organism: Homo sapiens (Human)
Disease: Homocystinuria
Category: Transformed cell line
Proper citation: RRID:CVCL_L974 Copy
https://web.expasy.org/cellosaurus/CVCL_X090
Organism: Homo sapiens (Human)
Disease: Cri du chat syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XX,del(5)(qter->p14) (Coriell=GM02337)., Population: Caucasian.
Proper citation: Coriell Cat# GM02337, RRID:CVCL_X090 Copy
https://web.expasy.org/cellosaurus/CVCL_L945
Organism: Homo sapiens (Human)
Disease: Familial adenomatous polyposis
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_L945 Copy
https://web.expasy.org/cellosaurus/CVCL_M996
Organism: Homo sapiens (Human)
Category: Transformed cell line
Proper citation: Coriell Cat# GM17321, RRID:CVCL_M996 Copy
https://web.expasy.org/cellosaurus/CVCL_1U23
Organism: Homo sapiens (Human)
Disease: Autosomal dominant torsion dystonia 1
Category: Transformed cell line
Proper citation: Coriell Cat# GM02347, RRID:CVCL_1U23 Copy
https://web.expasy.org/cellosaurus/CVCL_B5LN
Organism: Homo sapiens (Human)
Disease: Farber lipogranulomatosis
Category: Finite cell line
Proper citation: Coriell Cat# GM02351, RRID:CVCL_B5LN Copy
https://web.expasy.org/cellosaurus/CVCL_D862
Organism: Homo sapiens (Human)
Disease: Adenosine deaminase deficiency
Category: Finite cell line
Comments: Population: Hispanic.
Proper citation: RRID:CVCL_D862 Copy
https://web.expasy.org/cellosaurus/CVCL_B5LN
Organism: Homo sapiens (Human)
Disease: Farber lipogranulomatosis
Category: Finite cell line
Proper citation: RRID:CVCL_B5LN Copy
https://web.expasy.org/cellosaurus/CVCL_1U23
Organism: Homo sapiens (Human)
Disease: Autosomal dominant torsion dystonia 1
Category: Transformed cell line
Proper citation: RRID:CVCL_1U23 Copy
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