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_W110
Organism: Homo sapiens (Human)
Disease: Cornelia de Lange syndrome
Category: Finite cell line
Comments: Karyotypic information: 92,XXYY [12]; 46,XY [38] (Coriell=GM03478)., Population: Caucasian.
Proper citation: RRID:CVCL_W110 Copy
https://web.expasy.org/cellosaurus/CVCL_W008
Organism: Homo sapiens (Human)
Disease: Holocarboxylase synthetase deficiency
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_W008 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_UT34
Organism: Homo sapiens (Human)
Disease: Gyrate atrophy
Category: Transformed cell line
Proper citation: RRID:CVCL_UT34 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_UR75
Organism: Homo sapiens (Human)
Disease: Niemann-Pick disease
Category: Finite cell line
Proper citation: Coriell Cat# GM03519, RRID:CVCL_UR75 Copy
https://web.expasy.org/cellosaurus/CVCL_7394
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_7394 Copy
https://web.expasy.org/cellosaurus/CVCL_5M83
Organism: Homo sapiens (Human)
Disease: Down syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03503, RRID:CVCL_5M83 Copy
https://web.expasy.org/cellosaurus/CVCL_X291
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Transformed cell line
Proper citation: Coriell Cat# GM03543, RRID:CVCL_X291 Copy
https://web.expasy.org/cellosaurus/CVCL_W110
Organism: Homo sapiens (Human)
Disease: Cornelia de Lange syndrome
Category: Finite cell line
Comments: Karyotypic information: 92,XXYY [12]; 46,XY [38] (Coriell=GM03478)., Population: Caucasian.
Proper citation: Coriell Cat# GM03478, RRID:CVCL_W110 Copy
https://web.expasy.org/cellosaurus/CVCL_AD98
Organism: Homo sapiens (Human)
Disease: Jeune syndrome
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_AD98 Copy
https://web.expasy.org/cellosaurus/CVCL_F114
Organism: Homo sapiens (Human)
Disease: Bloom syndrome
Category: Finite cell line
Comments: Caution: Coriell has p.Cys1055fs*23 (c.3159delT) (3233delT) as the second mutation for this cell line., Donor information: From Bloom Syndrome Registry patient 87(AlFra) (BSR87)., Population: Caucasian; English and Jewish; Ashkenazi.
Proper citation: RRID:CVCL_F114 Copy
https://web.expasy.org/cellosaurus/CVCL_7391
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XY [35]; 46,XY,t(3;11)(3pter->3q24::11p15->11pter;11qter->11p15::3q24->3qter) [15] (Coriell=GM03523)., Population: Caucasian.
Proper citation: Coriell Cat# GM03523, RRID:CVCL_7391 Copy
https://web.expasy.org/cellosaurus/CVCL_X292
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03563, RRID:CVCL_X292 Copy
https://web.expasy.org/cellosaurus/CVCL_7393
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_7393 Copy
https://web.expasy.org/cellosaurus/CVCL_9S88
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: Coriell Cat# GM03535, RRID:CVCL_9S88 Copy
https://web.expasy.org/cellosaurus/CVCL_1L27
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03659, RRID:CVCL_1L27 Copy
https://web.expasy.org/cellosaurus/CVCL_F201
Organism: Homo sapiens (Human)
Disease: Menkes disease
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03700, RRID:CVCL_F201 Copy
https://web.expasy.org/cellosaurus/CVCL_7397
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_7397 Copy
https://web.expasy.org/cellosaurus/CVCL_X108
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_X108 Copy
https://web.expasy.org/cellosaurus/CVCL_V045
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03645, RRID:CVCL_V045 Copy
https://web.expasy.org/cellosaurus/CVCL_V042
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03642, RRID:CVCL_V042 Copy
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