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_AY28
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_AY28 Copy
https://web.expasy.org/cellosaurus/CVCL_1L29
Organism: Homo sapiens (Human)
Disease: Menkes disease
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_1L29 Copy
https://web.expasy.org/cellosaurus/CVCL_AY27
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Population: African American.
Proper citation: Coriell Cat# GM09145, RRID:CVCL_AY27 Copy
https://web.expasy.org/cellosaurus/CVCL_CY58
Organism: Homo sapiens (Human)
Disease: Gyrate atrophy
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_CY58 Copy
https://web.expasy.org/cellosaurus/CVCL_W576
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_W576 Copy
https://web.expasy.org/cellosaurus/CVCL_W300
Organism: Homo sapiens (Human)
Disease: Usher syndrome type 1
Category: Transformed cell line
Comments: Population: Caucasian; Acadian.
Proper citation: RRID:CVCL_W300 Copy
https://web.expasy.org/cellosaurus/CVCL_AY31
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_AY31 Copy
https://web.expasy.org/cellosaurus/CVCL_1R81
Organism: Homo sapiens (Human)
Disease:
Category: Hybrid cell line
Comments: Characteristics: Hybrid for chromosome X mapping (PubMed=9441767)., Group: Human/rodent somatic cell hybrid.
Proper citation: RRID:CVCL_1R81 Copy
https://web.expasy.org/cellosaurus/CVCL_1R81
Organism: Homo sapiens (Human)
Disease:
Category: Hybrid cell line
Comments: Characteristics: Hybrid for chromosome X mapping (PubMed=9441767)., Group: Human/rodent somatic cell hybrid.
Proper citation: Coriell Cat# GM09142, RRID:CVCL_1R81 Copy
https://web.expasy.org/cellosaurus/CVCL_N100
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; Italian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples.
Proper citation: RRID:CVCL_N100 Copy
https://web.expasy.org/cellosaurus/CVCL_AA71
Organism: Homo sapiens (Human)
Disease: Crigler-Najjar syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_AA71 Copy
https://web.expasy.org/cellosaurus/CVCL_5N94
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM09101, RRID:CVCL_5N94 Copy
https://web.expasy.org/cellosaurus/CVCL_5N97
Organism: Homo sapiens (Human)
Disease: Prader-Willi syndrome
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM09189, RRID:CVCL_5N97 Copy
https://web.expasy.org/cellosaurus/CVCL_AY27
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_AY27 Copy
https://web.expasy.org/cellosaurus/CVCL_CY61
Organism: Homo sapiens (Human)
Disease: Gyrate atrophy
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM09116, RRID:CVCL_CY61 Copy
https://web.expasy.org/cellosaurus/CVCL_CY62
Organism: Homo sapiens (Human)
Disease: Gyrate atrophy
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_CY62 Copy
https://web.expasy.org/cellosaurus/CVCL_V823
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: African American.
Proper citation: Coriell Cat# GM09216, RRID:CVCL_V823 Copy
https://web.expasy.org/cellosaurus/CVCL_N100
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; Italian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples.
Proper citation: Coriell Cat# GM09196, RRID:CVCL_N100 Copy
https://web.expasy.org/cellosaurus/CVCL_CY59
Organism: Homo sapiens (Human)
Disease: Gyrate atrophy
Category: Finite cell line
Comments: Population: Caucasian; Irish.
Proper citation: RRID:CVCL_CY59 Copy
https://web.expasy.org/cellosaurus/CVCL_1L53
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian; German/Swiss.
Proper citation: RRID:CVCL_1L53 Copy
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