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_B0IR
Organism: Homo sapiens (Human)
Disease: Leigh disease
Category: Finite cell line
Comments: Population: Caucasian; Austrian.
Proper citation: RRID:CVCL_B0IR Copy
https://web.expasy.org/cellosaurus/CVCL_A5MF
Organism: Homo sapiens (Human)
Disease: Multicentric carpotarsal osteolysis syndrome
Category: Transformed cell line
Comments:
Proper citation: RRID:CVCL_A5MF Copy
https://web.expasy.org/cellosaurus/CVCL_A5MJ
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian; Polish.
Proper citation: RRID:CVCL_A5MJ Copy
https://web.expasy.org/cellosaurus/CVCL_A2TV
Organism: Homo sapiens (Human)
Disease: SLC6A1-associated myoclonic-atonic epilepsy
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_A2TV Copy
https://web.expasy.org/cellosaurus/CVCL_A2TR
Organism: Homo sapiens (Human)
Disease: Intellectual developmental disorder, autosomal dominant 9
Category: Induced pluripotent stem cell
Comments:
Proper citation: RRID:CVCL_A2TR Copy
https://web.expasy.org/cellosaurus/CVCL_A2YS
Organism: Homo sapiens (Human)
Disease: Leigh disease
Category: Finite cell line
Comments: Population: Indian.
Proper citation: RRID:CVCL_A2YS Copy
https://web.expasy.org/cellosaurus/CVCL_ZW46
Organism: Homo sapiens (Human)
Disease: Cerebral creatine deficiency syndrome 1
Category: Finite cell line
Comments: Population: Caucasian; German.
Proper citation: RRID:CVCL_ZW46 Copy
https://web.expasy.org/cellosaurus/CVCL_A2YN
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM28009, RRID:CVCL_A2YN Copy
https://web.expasy.org/cellosaurus/CVCL_A2SS
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian; Spanish (Chilean).
Proper citation: Coriell Cat# GM27873, RRID:CVCL_A2SS Copy
https://web.expasy.org/cellosaurus/CVCL_B0I4
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM28035, RRID:CVCL_B0I4 Copy
https://web.expasy.org/cellosaurus/CVCL_A2TF
Organism: Homo sapiens (Human)
Disease: Nemaline myopathy 3
Category: Transformed cell line
Comments: Population: Jewish; Ashkenazi.
Proper citation: RRID:CVCL_A2TF Copy
https://web.expasy.org/cellosaurus/CVCL_A2TB
Organism: Homo sapiens (Human)
Disease: Rett syndrome, congenital variant
Category: Induced pluripotent stem cell
Comments:
Proper citation: RRID:CVCL_A2TB Copy
https://web.expasy.org/cellosaurus/CVCL_ZW54
Organism: Homo sapiens (Human)
Disease: Cerebral creatine deficiency syndrome 1
Category: Finite cell line
Comments:
Proper citation: Coriell Cat# GM27888, RRID:CVCL_ZW54 Copy
https://web.expasy.org/cellosaurus/CVCL_B3SE
Organism: Homo sapiens (Human)
Disease: Leigh disease
Category: Finite cell line
Comments: Population: Indian.
Proper citation: RRID:CVCL_B3SE Copy
https://web.expasy.org/cellosaurus/CVCL_A2SQ
Organism: Homo sapiens (Human)
Disease: Rett syndrome, congenital variant
Category: Transformed cell line
Comments: Population: Caucasian; Spanish (Chilean).
Proper citation: RRID:CVCL_A2SQ Copy
https://web.expasy.org/cellosaurus/CVCL_ZW57
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Jewish; Ashkenazi.
Proper citation: RRID:CVCL_ZW57 Copy
https://web.expasy.org/cellosaurus/CVCL_A5MK
Organism: Homo sapiens (Human)
Disease: Intellectual developmental disorder, autosomal dominant 5
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_A5MK Copy
https://web.expasy.org/cellosaurus/CVCL_A2TT
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM27904, RRID:CVCL_A2TT Copy
https://web.expasy.org/cellosaurus/CVCL_B0I5
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM28036, RRID:CVCL_B0I5 Copy
https://web.expasy.org/cellosaurus/CVCL_A2TU
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_A2TU Copy
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