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_JC90
Organism: Homo sapiens (Human)
Disease: Androgen insensitivity syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XY; but phenotypically female (Coriell=GM01404)., Population: African American.
Proper citation: RRID:CVCL_JC90 Copy
https://web.expasy.org/cellosaurus/CVCL_4N09
Organism: Homo sapiens (Human)
Disease: Hyperlipoproteinemia, type IIa
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_4N09 Copy
https://web.expasy.org/cellosaurus/CVCL_7319
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM01381, RRID:CVCL_7319 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_DF17
Organism: Homo sapiens (Human)
Disease: Retinoblastoma
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_DF17 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_DF17
Organism: Homo sapiens (Human)
Disease: Retinoblastoma
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM01408, RRID:CVCL_DF17 Copy
https://web.expasy.org/cellosaurus/CVCL_2H15
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Caution: Indicated by Coriell to originate from father of GM01374 but does not contain the same CBS mutation, therefore the pedigree relationship may be incorrect (PubMed=8528202)., Population: Caucasian.
Proper citation: RRID:CVCL_2H15 Copy
https://web.expasy.org/cellosaurus/CVCL_0M01
Organism: Homo sapiens (Human)
Disease: Mucopolysaccharidosis type IIIB
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_0M01 Copy
https://web.expasy.org/cellosaurus/CVCL_J114
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,+der(9)(9pter->9q21.2::13q12.1->13qter)mat,-13 (Coriell=GM01387)., Population: Caucasian.
Proper citation: Coriell Cat# GM01387, RRID:CVCL_J114 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_JD99
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM01420, RRID:CVCL_JD99 Copy
https://web.expasy.org/cellosaurus/CVCL_AI26
Organism: Homo sapiens (Human)
Disease: Hepatocyte nuclear factor 4-alpha associated monogenic diabetes
Category: Finite cell line
Comments: Population: Caucasian., Part of: R-W pedigree MODY cell line collection.
Proper citation: RRID:CVCL_AI26 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_GY15
Organism: Homo sapiens (Human)
Disease: Hereditary persistence of fetal hemoglobin
Category: Finite cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_GY15 Copy
https://web.expasy.org/cellosaurus/CVCL_0M11
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM01444, RRID:CVCL_0M11 Copy
https://web.expasy.org/cellosaurus/CVCL_4N08
Organism: Homo sapiens (Human)
Disease: Hyperlipoproteinemia, type IIa
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_4N08 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_DF17
Organism: Homo sapiens (Human)
Disease: Retinoblastoma
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# AG01408, RRID:CVCL_DF17 Copy
https://web.expasy.org/cellosaurus/CVCL_8517
Organism: Homo sapiens (Human)
Disease: Adenosine deaminase deficiency
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_8517 Copy
https://web.expasy.org/cellosaurus/CVCL_2H17
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM01447, RRID:CVCL_2H17 Copy
https://web.expasy.org/cellosaurus/CVCL_1V13
Organism: Homo sapiens (Human)
Disease: Hurler syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM01391, RRID:CVCL_1V13 Copy
https://web.expasy.org/cellosaurus/CVCL_AE18
Organism: Homo sapiens (Human)
Disease: Abetalipoproteinemia
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_AE18 Copy
https://web.expasy.org/cellosaurus/CVCL_4N10
Organism: Homo sapiens (Human)
Disease: Cutis laxa
Category: Finite cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_4N10 Copy
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