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_X286
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_X286 Copy
https://web.expasy.org/cellosaurus/CVCL_X287
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_X287 Copy
https://web.expasy.org/cellosaurus/CVCL_X288
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03493, RRID:CVCL_X288 Copy
https://web.expasy.org/cellosaurus/CVCL_F108
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM03470, RRID:CVCL_F108 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_2Y96
Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_2Y96 Copy
https://web.expasy.org/cellosaurus/CVCL_1N77
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_1N77 Copy
https://web.expasy.org/cellosaurus/CVCL_X294
Organism: Homo sapiens (Human)
Disease: 22q11.2 deletion syndrome
Category: Finite cell line
Comments: Karyotypic information: 45,XY,der(3)(3pter->3q29::22q11->22qter),-22 (Coriell=GM03577)., Population: Caucasian.
Proper citation: Coriell Cat# GM03577, RRID:CVCL_X294 Copy
https://web.expasy.org/cellosaurus/CVCL_1N77
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03501, RRID:CVCL_1N77 Copy
https://web.expasy.org/cellosaurus/CVCL_X288
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_X288 Copy
https://web.expasy.org/cellosaurus/CVCL_7390
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Mexican., Part of: Human variation panel.
Proper citation: RRID:CVCL_7390 Copy
https://web.expasy.org/cellosaurus/CVCL_F657
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_F657 Copy
https://web.expasy.org/cellosaurus/CVCL_X246
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,X,der(9)t(X;9)(q34;q12) (PubMed=10377420)., Population: African American.
Proper citation: RRID:CVCL_X246 Copy
https://web.expasy.org/cellosaurus/CVCL_F657
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM01416, RRID:CVCL_F657 Copy
https://web.expasy.org/cellosaurus/CVCL_X246
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,X,der(9)t(X;9)(q34;q12) (PubMed=10377420)., Population: African American.
Proper citation: Coriell Cat# GM01414, RRID:CVCL_X246 Copy
https://web.expasy.org/cellosaurus/CVCL_X080
Organism: Homo sapiens (Human)
Disease: Trisomy 18
Category: Finite cell line
Comments: Karyotypic information: 47,XY,+18.arr(18)x3 (Coriell=GM01359)., Population: Caucasian.
Proper citation: RRID:CVCL_X080 Copy
https://web.expasy.org/cellosaurus/CVCL_X251
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_X251 Copy
https://web.expasy.org/cellosaurus/CVCL_X250
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: African American.
Proper citation: Coriell Cat# GM01535, RRID:CVCL_X250 Copy
https://web.expasy.org/cellosaurus/CVCL_X081
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM01549, RRID:CVCL_X081 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_F130
Organism: Homo sapiens (Human)
Disease: Sporadic retinoblastoma
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_F130 Copy
https://web.expasy.org/cellosaurus/CVCL_5M69
Organism: Homo sapiens (Human)
Disease: Neurofibromatosis type 1
Category: Transformed cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_5M69 Copy
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