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_JX69
Organism: Homo sapiens (Human)
Disease: Prune belly syndrome
Category: Finite cell line
Proper citation: Coriell Cat# GM16555, RRID:CVCL_JX69 Copy
https://web.expasy.org/cellosaurus/CVCL_G042
Organism: Homo sapiens (Human)
Disease: Fanconi anemia, complementation group D2
Category: Transformed cell line
Proper citation: RRID:CVCL_G042 Copy
https://web.expasy.org/cellosaurus/CVCL_0G75
Organism: Homo sapiens (Human)
Disease: Holoprosencephaly
Category: Transformed cell line
Proper citation: Coriell Cat# GM16586, RRID:CVCL_0G75 Copy
https://web.expasy.org/cellosaurus/CVCL_5Q72
Organism: Cricetulus griseus (Chinese hamster)
Category: Hybrid cell line
Comments: Group: Human/rodent somatic cell hybrid.
Proper citation: RRID:CVCL_5Q72 Copy
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_5Q76
Organism: Homo sapiens (Human)
Disease: Azoospermia
Category: Transformed cell line
Comments: Population: Southeast Asian; Vietnamese.
Proper citation: RRID:CVCL_5Q76 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
https://web.expasy.org/cellosaurus/CVCL_HJ88
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Latino or Hispanic.
Proper citation: Coriell Cat# GM16647, RRID:CVCL_HJ88 Copy
https://web.expasy.org/cellosaurus/CVCL_AB36
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Chinese., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples.
Proper citation: RRID:CVCL_AB36 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_IW03
Organism: Homo sapiens (Human)
Disease: Leigh disease
Category: Hybrid cell line
Comments: Characteristics: Cytoplasmic transfer (cybrid) produced by the fusion of Leigh syndrome enucleated cells GM13740 (Cellosaurus=CVCL_8A62) with cell line devoid of mitochondrial DNA (rho0) derived from 143B (Cellosaurus=CVCL_2270).
Proper citation: Coriell Cat# GM16530, RRID:CVCL_IW03 Copy
https://web.expasy.org/cellosaurus/CVCL_5Q68
Organism: Homo sapiens (Human)
Disease: Deletion 18p syndrome
Category: Transformed cell line
Proper citation: RRID:CVCL_5Q68 Copy
https://web.expasy.org/cellosaurus/CVCL_HJ90
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Latino or Hispanic.
Proper citation: Coriell Cat# GM16649, RRID:CVCL_HJ90 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_5Q74
Organism: Homo sapiens (Human)
Disease: Cri du chat syndrome
Category: Transformed cell line
Proper citation: Coriell Cat# GM16598, RRID:CVCL_5Q74 Copy
https://web.expasy.org/cellosaurus/CVCL_0G76
Organism: Cricetulus griseus (Chinese hamster)
Category: Hybrid cell line
Comments: Group: Human/rodent somatic cell hybrid.
Proper citation: Coriell Cat# GM16587, RRID:CVCL_0G76 Copy
https://web.expasy.org/cellosaurus/CVCL_HJ86
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Latino or Hispanic.
Proper citation: RRID:CVCL_HJ86 Copy
https://web.expasy.org/cellosaurus/CVCL_DB92
Organism: Homo sapiens (Human)
Disease: Hereditary melanoma with CDKN2A mutation
Category: Transformed cell line
Comments: Donor information: At sampling donor was not affected with cutaneous malignant melanoma 2 but at risk for disease (mutation in CDKN2A start site).
Proper citation: RRID:CVCL_DB92 Copy
https://web.expasy.org/cellosaurus/CVCL_N267
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Human variation panel.
Proper citation: Coriell Cat# GM18097, RRID:CVCL_N267 Copy
https://web.expasy.org/cellosaurus/CVCL_5Q71
Organism: Homo sapiens (Human)
Disease: Cri du chat syndrome
Category: Transformed cell line
Proper citation: RRID:CVCL_5Q71 Copy
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