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_2S98
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(4;9)(4pter->4q33::9q12->9qter;9pter->9q12::4q33->4qter) (Coriell=GM03886)., Population: Caucasian.
Proper citation: RRID:CVCL_2S98 Copy
https://web.expasy.org/cellosaurus/CVCL_1H65
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_1H65 Copy
https://web.expasy.org/cellosaurus/CVCL_1H70
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03865, RRID:CVCL_1H70 Copy
https://web.expasy.org/cellosaurus/CVCL_1H73
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03868, RRID:CVCL_1H73 Copy
https://web.expasy.org/cellosaurus/CVCL_AK88
Organism: Homo sapiens (Human)
Disease: Retinitis pigmentosa
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03837, RRID:CVCL_AK88 Copy
https://web.expasy.org/cellosaurus/CVCL_GY19
Organism: Homo sapiens (Human)
Disease: Leber congenital amaurosis
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03851, RRID:CVCL_GY19 Copy
https://web.expasy.org/cellosaurus/CVCL_2T00
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(1;4)(1pter->1q32::4p16->4pter;4qter->4p16::1q32->1qter) (Coriell=GM04088)., Population: Caucasian.
Proper citation: RRID:CVCL_2T00 Copy
https://web.expasy.org/cellosaurus/CVCL_CY42
Organism: Homo sapiens (Human)
Disease: Familial adenomatous polyposis
Category: Transformed cell line
Comments: Donor information: At sampling donor was not affected with familial adenomatous polyposis but at risk for disease., Population: Caucasian.
Proper citation: RRID:CVCL_CY42 Copy
https://web.expasy.org/cellosaurus/CVCL_V240
Organism: Ovis aries (Sheep)
Disease:
Category: Finite cell line
Comments:
Proper citation: RRID:CVCL_V240 Copy
https://web.expasy.org/cellosaurus/CVCL_0R01
Organism: Homo sapiens (Human)
Disease: Primary carnitine deficiency
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_0R01 Copy
https://web.expasy.org/cellosaurus/CVCL_V820
Organism: Homo sapiens (Human)
Disease: Wolf-Hirschhorn syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_V820 Copy
https://web.expasy.org/cellosaurus/CVCL_T821
Organism: Homo sapiens (Human)
Disease: Friedreich ataxia
Category: Transformed cell line
Comments: Caution: Indicated by Coriell to have 420 and 541 GAA repeats., Population: Caucasian.
Proper citation: RRID:CVCL_T821 Copy
https://web.expasy.org/cellosaurus/CVCL_N013
Organism: Homo sapiens (Human)
Disease: Dystrophia myotonica 1
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Human variation panel.
Proper citation: RRID:CVCL_N013 Copy
https://web.expasy.org/cellosaurus/CVCL_N013
Organism: Homo sapiens (Human)
Disease: Dystrophia myotonica 1
Category: Transformed cell line
Comments: Population: Caucasian., Part of: Human variation panel.
Proper citation: Coriell Cat# GM18013, RRID:CVCL_N013 Copy
https://web.expasy.org/cellosaurus/CVCL_IZ39
Organism: Homo sapiens (Human)
Disease: Hyperlipoproteinemia, type I
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_IZ39 Copy
https://web.expasy.org/cellosaurus/CVCL_CY31
Organism: Homo sapiens (Human)
Disease: Familial adenomatous polyposis
Category: Finite cell line
Comments: Donor information: At sampling donor was not affected with familial adenomatous polyposis but at risk for disease., Population: Caucasian.
Proper citation: RRID:CVCL_CY31 Copy
https://web.expasy.org/cellosaurus/CVCL_CY35
Organism: Homo sapiens (Human)
Disease: Familial adenomatous polyposis
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_CY35 Copy
https://web.expasy.org/cellosaurus/CVCL_1N28
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_1N28 Copy
https://web.expasy.org/cellosaurus/CVCL_CY32
Organism: Homo sapiens (Human)
Disease: Familial adenomatous polyposis
Category: Transformed cell line
Comments: Donor information: At sampling donor was not affected with familial adenomatous polyposis but at risk for disease., Population: Caucasian.
Proper citation: Coriell Cat# GM03941, RRID:CVCL_CY32 Copy
https://web.expasy.org/cellosaurus/CVCL_X115
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_X115 Copy
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