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_CW69
Organism: Homo sapiens (Human)
Disease: Schizophrenia
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_CW69 Copy
https://web.expasy.org/cellosaurus/CVCL_U703
Organism: Homo sapiens (Human)
Disease: Bloom syndrome
Category: Finite cell line
Comments: Donor information: From Bloom Syndrome Registry patient 53(StAs) (BSR53)., Population: Jewish; Ashkenazi.
Proper citation: RRID:CVCL_U703 Copy
https://web.expasy.org/cellosaurus/CVCL_1H41
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_1H41 Copy
https://web.expasy.org/cellosaurus/CVCL_M994
Organism: Homo sapiens (Human)
Disease: Hereditary persistence of fetal hemoglobin
Category: Transformed cell line
Comments: Population: Africans south of the Sahara., Part of: Human variation panel.
Proper citation: RRID:CVCL_M994 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_L962
Organism: Homo sapiens (Human)
Disease: Hyperlipoproteinemia, type IIa
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM02110, RRID:CVCL_L962 Copy
https://web.expasy.org/cellosaurus/CVCL_M990
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Arab., Part of: Human variation panel.
Proper citation: RRID:CVCL_M990 Copy
https://web.expasy.org/cellosaurus/CVCL_H177
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_H177 Copy
https://web.expasy.org/cellosaurus/CVCL_W640
Organism: Homo sapiens (Human)
Disease: I-cell disease
Category: Finite cell line
Comments: Population: Arab.
Proper citation: RRID:CVCL_W640 Copy
https://web.expasy.org/cellosaurus/CVCL_CW70
Organism: Homo sapiens (Human)
Disease: Chediak-Higashi syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_CW70 Copy
https://web.expasy.org/cellosaurus/CVCL_V825
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_V825 Copy
https://web.expasy.org/cellosaurus/CVCL_V030
Organism: Homo sapiens (Human)
Disease: Argininemia
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_V030 Copy
https://web.expasy.org/cellosaurus/CVCL_W621
Organism: Homo sapiens (Human)
Disease: Wolman disease
Category: Finite cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_W621 Copy
https://web.expasy.org/cellosaurus/CVCL_2Z72
Organism: Homo sapiens (Human)
Disease: Nevoid basal cell carcinoma syndrome
Category: Finite cell line
Comments: Characteristics: Hypersensitive to cell killing by ionizing radiation (Coriell=GM02098)., Population: Caucasian.
Proper citation: RRID:CVCL_2Z72 Copy
https://web.expasy.org/cellosaurus/CVCL_6B42
Organism: Homo sapiens (Human)
Disease: Metachromatic leukodystrophy
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM02093, RRID:CVCL_6B42 Copy
https://web.expasy.org/cellosaurus/CVCL_1H40
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 50% risk for disease., Population: Caucasian.
Proper citation: Coriell Cat# GM02078, RRID:CVCL_1H40 Copy
https://web.expasy.org/cellosaurus/CVCL_1N60
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(6;7)(6pter->6q27::7q22->7qter;7pter->7q22::6q27->6qter) (Coriell=GM02068)., Population: Caucasian.
Proper citation: Coriell Cat# GM02068, RRID:CVCL_1N60 Copy
https://web.expasy.org/cellosaurus/CVCL_1Y44
Organism: Homo sapiens (Human)
Disease: Sandhoff disease
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM02094, RRID:CVCL_1Y44 Copy
https://web.expasy.org/cellosaurus/CVCL_F593
Organism: Homo sapiens (Human)
Disease: Fanconi anemia
Category: Finite cell line
Comments: Population: Arab.
Proper citation: RRID:CVCL_F593 Copy
https://web.expasy.org/cellosaurus/CVCL_1H40
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 50% risk for disease., Population: Caucasian.
Proper citation: RRID:CVCL_1H40 Copy
https://web.expasy.org/cellosaurus/CVCL_X260
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;Y)(q11;q11) (PubMed=10377420)., Population: Caucasian.
Proper citation: Coriell Cat# GM02103, RRID:CVCL_X260 Copy
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