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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_DA81
Organism: Homo sapiens (Human)
Disease: Congenital disorder of glycosylation type Ig
Category: Finite cell line
Proper citation: RRID:CVCL_DA81 Copy
https://web.expasy.org/cellosaurus/CVCL_8A69
Organism: Homo sapiens (Human)
Disease: Farber lipogranulomatosis
Category: Finite cell line
Comments: Population: Tunisian.
Proper citation: RRID:CVCL_8A69 Copy
https://web.expasy.org/cellosaurus/CVCL_1L16
Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type II
Category: Finite cell line
Proper citation: RRID:CVCL_1L16 Copy
https://web.expasy.org/cellosaurus/CVCL_9Y51
Organism: Homo sapiens (Human)
Disease: Donohue syndrome
Category: Finite cell line
Comments: Population: Turkish.
Proper citation: RRID:CVCL_9Y51 Copy
https://web.expasy.org/cellosaurus/CVCL_1L20
Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type II
Category: Finite cell line
Comments: Population: African American.
Proper citation: RRID:CVCL_1L20 Copy
https://web.expasy.org/cellosaurus/CVCL_0R35
Organism: Homo sapiens (Human)
Disease: Gaucher disease
Category: Finite cell line
Comments: Population: Lebanese.
Proper citation: RRID:CVCL_0R35 Copy
https://web.expasy.org/cellosaurus/CVCL_0R42
Organism: Homo sapiens (Human)
Disease: Gaucher disease
Category: Finite cell line
Proper citation: RRID:CVCL_0R42 Copy
https://web.expasy.org/cellosaurus/CVCL_1L23
Organism: Homo sapiens (Human)
Disease: Glycogen storage disease type II
Category: Finite cell line
Comments: Population: Bangladeshi.
Proper citation: RRID:CVCL_1L23 Copy
https://web.expasy.org/cellosaurus/CVCL_U304
Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line
Proper citation: RRID:CVCL_U304 Copy
https://web.expasy.org/cellosaurus/CVCL_U300
Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line
Proper citation: RRID:CVCL_U300 Copy
https://web.expasy.org/cellosaurus/CVCL_U305
Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line
Proper citation: RRID:CVCL_U305 Copy
https://web.expasy.org/cellosaurus/CVCL_U301
Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line
Proper citation: RRID:CVCL_U301 Copy
https://web.expasy.org/cellosaurus/CVCL_U302
Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line
Proper citation: RRID:CVCL_U302 Copy
https://web.expasy.org/cellosaurus/CVCL_U303
Organism: Homo sapiens (Human)
Disease: Lesch-Nyhan syndrome
Category: Finite cell line
Proper citation: RRID:CVCL_U303 Copy
https://web.expasy.org/cellosaurus/CVCL_DA99
Organism: Homo sapiens (Human)
Disease: Neuronal ceroid lipofuscinosis type 1
Category: Finite cell line
Proper citation: RRID:CVCL_DA99 Copy
https://web.expasy.org/cellosaurus/CVCL_GY30
Organism: Homo sapiens (Human)
Disease: Molybdenum cofactor deficiency
Category: Finite cell line
Proper citation: Coriell Cat# GM20415, RRID:CVCL_GY30 Copy
https://web.expasy.org/cellosaurus/CVCL_GY30
Organism: Homo sapiens (Human)
Disease: Molybdenum cofactor deficiency
Category: Finite cell line
Proper citation: RRID:CVCL_GY30 Copy
https://web.expasy.org/cellosaurus/CVCL_IM22
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: Chimera 46,XX/46,XY., Population: Chinese; Taiwan.
Proper citation: RRID:CVCL_IM22 Copy
https://web.expasy.org/cellosaurus/CVCL_IM22
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: Chimera 46,XX/46,XY., Population: Chinese; Taiwan.
Proper citation: Coriell Cat# GM20486, RRID:CVCL_IM22 Copy
https://web.expasy.org/cellosaurus/CVCL_DS98
Organism: Homo sapiens (Human)
Disease: Nephrotic syndrome - NPHS1 associated
Category: Finite cell line
Proper citation: RRID:CVCL_DS98 Copy
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