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_HJ93
Organism: Homo sapiens (Human)
Disease: Trichothiodystrophy
Category: Finite cell line
Comments: Population: Latino or Hispanic.
Proper citation: Coriell Cat# GM16652, RRID:CVCL_HJ93 Copy
https://web.expasy.org/cellosaurus/CVCL_4F42
Organism: Homo sapiens (Human)
Disease: Rett syndrome
Category: Finite cell line
Proper citation: RRID:CVCL_4F42 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_YP91
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM16733, RRID:CVCL_YP91 Copy
https://web.expasy.org/cellosaurus/CVCL_X436
Organism: Homo sapiens (Human)
Disease: Smith-Lemli-Opitz syndrome
Category: Finite cell line
Proper citation: Coriell Cat# GM16549, RRID:CVCL_X436 Copy
https://web.expasy.org/cellosaurus/CVCL_9Y36
Organism: Homo sapiens (Human)
Disease: Rhizomelic chondrodysplasia punctata
Category: Finite cell line
Comments: Population: Lebanese.
Proper citation: RRID:CVCL_9Y36 Copy
https://web.expasy.org/cellosaurus/CVCL_AK40
Organism: Homo sapiens (Human)
Disease: Fanconi anemia, complementation group A
Category: Finite cell line
Proper citation: Coriell Cat# GM16631, RRID:CVCL_AK40 Copy
https://web.expasy.org/cellosaurus/CVCL_HJ91
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Latino or Hispanic.
Proper citation: Coriell Cat# GM16650, RRID:CVCL_HJ91 Copy
https://web.expasy.org/cellosaurus/CVCL_H528
Organism: Homo sapiens (Human)
Disease: Rett syndrome
Category: Finite cell line
Proper citation: Coriell Cat# GM16563, RRID:CVCL_H528 Copy
https://web.expasy.org/cellosaurus/CVCL_5Q78
Organism: Homo sapiens (Human)
Disease: Deafness
Category: Finite cell line
Proper citation: RRID:CVCL_5Q78 Copy
https://web.expasy.org/cellosaurus/CVCL_1F68
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_1F68 Copy
https://web.expasy.org/cellosaurus/CVCL_4F75
Organism: Homo sapiens (Human)
Disease: Peroxisome biogenesis disorder 7A
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM16866, RRID:CVCL_4F75 Copy
https://web.expasy.org/cellosaurus/CVCL_4D34
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian; Amish.
Proper citation: Coriell Cat# GM16968, RRID:CVCL_4D34 Copy
https://web.expasy.org/cellosaurus/CVCL_4F75
Organism: Homo sapiens (Human)
Disease: Peroxisome biogenesis disorder 7A
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_4F75 Copy
https://web.expasy.org/cellosaurus/CVCL_4D25
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian; Amish.
Proper citation: RRID:CVCL_4D25 Copy
https://web.expasy.org/cellosaurus/CVCL_4D32
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian; Amish.
Proper citation: RRID:CVCL_4D32 Copy
https://web.expasy.org/cellosaurus/CVCL_4D28
Organism: Homo sapiens (Human)
Disease: Osteogenesis imperfecta type IV
Category: Finite cell line
Comments: Population: Caucasian; Amish.
Proper citation: RRID:CVCL_4D28 Copy
https://web.expasy.org/cellosaurus/CVCL_1F68
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM16800, RRID:CVCL_1F68 Copy
https://web.expasy.org/cellosaurus/CVCL_9Z52
Organism: Homo sapiens (Human)
Disease: Peroxisome biogenesis disorder 7B
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_9Z52 Copy
https://web.expasy.org/cellosaurus/CVCL_AK43
Organism: Homo sapiens (Human)
Disease: Fanconi anemia, complementation group C
Category: Finite cell line
Proper citation: Coriell Cat# GM16754, RRID:CVCL_AK43 Copy
https://web.expasy.org/cellosaurus/CVCL_4D23
Organism: Homo sapiens (Human)
Disease: Osteogenesis imperfecta type IV
Category: Finite cell line
Comments: Population: Caucasian; Amish.
Proper citation: RRID:CVCL_4D23 Copy
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