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.
Discontinued
https://web.expasy.org/cellosaurus/CVCL_L969
Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM01514, RRID:CVCL_L969 Copy
Discontinued
https://web.expasy.org/cellosaurus/CVCL_L969
Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM02206, RRID:CVCL_L969 Copy
https://web.expasy.org/cellosaurus/CVCL_CZ04
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM02209, RRID:CVCL_CZ04 Copy
https://web.expasy.org/cellosaurus/CVCL_1U22
Organism: Homo sapiens (Human)
Disease: Autosomal dominant torsion dystonia 1
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_1U22 Copy
https://web.expasy.org/cellosaurus/CVCL_4J48
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: Coriell Cat# GM02229, RRID:CVCL_4J48 Copy
https://web.expasy.org/cellosaurus/CVCL_4J49
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_4J49 Copy
https://web.expasy.org/cellosaurus/CVCL_M995
Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome
Category: Finite cell line
Comments: Population: Cuban., Part of: Human variation panel.
Proper citation: RRID:CVCL_M995 Copy
https://web.expasy.org/cellosaurus/CVCL_1U21
Organism: Homo sapiens (Human)
Disease: Autosomal dominant torsion dystonia 1
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM02304, RRID:CVCL_1U21 Copy
https://web.expasy.org/cellosaurus/CVCL_BT13
Organism: Homo sapiens (Human)
Disease: Beta thalassemia
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_BT13 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_CX22
Organism: Homo sapiens (Human)
Disease: Lactic acidosis
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM02224, RRID:CVCL_CX22 Copy
https://web.expasy.org/cellosaurus/CVCL_X261
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,9qh+,t(16;22)(16qter->16p13.11::22q11.21->22qter;22pter->22q11.21::16p13.11->16pter) (Coriell=GM02324)., Population: Caucasian.
Proper citation: Coriell Cat# GM02324, RRID:CVCL_X261 Copy
https://web.expasy.org/cellosaurus/CVCL_M995
Organism: Homo sapiens (Human)
Disease: Ehlers-Danlos syndrome
Category: Finite cell line
Comments: Population: Cuban., Part of: Human variation panel.
Proper citation: Coriell Cat# GM17353, RRID:CVCL_M995 Copy
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)
Disease:
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)
Disease:
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_K509
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian., Part of: ECACC randomly selected UK Caucasian blood donors cell line selection.
Proper citation: ECACC Cat# 94060867, RRID:CVCL_K509 Copy
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