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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_U396
Organism: Homo sapiens (Human)
Disease: Tay-Sachs disease
Category: Transformed cell line
Proper citation: RRID:CVCL_U396 Copy
https://web.expasy.org/cellosaurus/CVCL_AK79
Organism: Homo sapiens (Human)
Disease: Retinitis pigmentosa
Category: Finite cell line
Comments: Population: Caucasian; German.
Proper citation: Coriell Cat# GM03824, RRID:CVCL_AK79 Copy
https://web.expasy.org/cellosaurus/CVCL_1H63
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian.
Proper citation: Coriell Cat# GM03748, RRID:CVCL_1H63 Copy
https://web.expasy.org/cellosaurus/CVCL_X111
Organism: Homo sapiens (Human)
Disease: Deletion 18p syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XY,del(18)(qter->p11) (Coriell=GM03767)., Population: Caucasian.
Proper citation: RRID:CVCL_X111 Copy
https://web.expasy.org/cellosaurus/CVCL_F174
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_F174 Copy
https://web.expasy.org/cellosaurus/CVCL_AK81
Organism: Homo sapiens (Human)
Disease: Retinitis pigmentosa
Category: Finite cell line
Comments: Population: Caucasian; German.
Proper citation: Coriell Cat# GM03826, RRID:CVCL_AK81 Copy
https://web.expasy.org/cellosaurus/CVCL_M945
Organism: Homo sapiens (Human)
Disease: Dystrophia myotonica 1
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_M945 Copy
https://web.expasy.org/cellosaurus/CVCL_U396
Organism: Homo sapiens (Human)
Disease: Tay-Sachs disease
Category: Transformed cell line
Proper citation: Coriell Cat# GM03771, RRID:CVCL_U396 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_BW99
Organism: Homo sapiens (Human)
Disease: Central core disease
Category: Finite cell line
Proper citation: RRID:CVCL_BW99 Copy
https://web.expasy.org/cellosaurus/CVCL_AK80
Organism: Homo sapiens (Human)
Disease: Retinitis pigmentosa
Category: Transformed cell line
Comments: Population: Caucasian; German.
Proper citation: RRID:CVCL_AK80 Copy
https://web.expasy.org/cellosaurus/CVCL_F221
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: African American.
Proper citation: Coriell Cat# GM03724, RRID:CVCL_F221 Copy
https://web.expasy.org/cellosaurus/CVCL_M942
Organism: Homo sapiens (Human)
Disease: Duchenne muscular dystrophy
Category: Transformed cell line
Comments: Population: Caucasian; Iberian., Part of: Human variation panel.
Proper citation: RRID:CVCL_M942 Copy
https://web.expasy.org/cellosaurus/CVCL_AK80
Organism: Homo sapiens (Human)
Disease: Retinitis pigmentosa
Category: Transformed cell line
Comments: Population: Caucasian; German.
Proper citation: Coriell Cat# GM03825, RRID:CVCL_AK80 Copy
https://web.expasy.org/cellosaurus/CVCL_DF22
Organism: Homo sapiens (Human)
Disease: Macular dystrophy, retinal, 1
Category: Transformed cell line
Proper citation: Coriell Cat# GM03784, RRID:CVCL_DF22 Copy
https://web.expasy.org/cellosaurus/CVCL_X111
Organism: Homo sapiens (Human)
Disease: Deletion 18p syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XY,del(18)(qter->p11) (Coriell=GM03767)., Population: Caucasian.
Proper citation: Coriell Cat# GM03767, RRID:CVCL_X111 Copy
https://web.expasy.org/cellosaurus/CVCL_AK78
Organism: Homo sapiens (Human)
Disease: Retinitis pigmentosa
Category: Transformed cell line
Comments: Population: Caucasian; German.
Proper citation: Coriell Cat# GM03823, RRID:CVCL_AK78 Copy
https://web.expasy.org/cellosaurus/CVCL_1H62
Organism: Homo sapiens (Human)
Disease: Huntington's disease
Category: Transformed cell line
Comments: Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease.
Proper citation: RRID:CVCL_1H62 Copy
https://web.expasy.org/cellosaurus/CVCL_F172
Organism: Homo sapiens (Human)
Disease: Spinal muscular atrophy type 2
Category: Finite cell line
Comments: Population: Caucasian., Problematic cell line: Misclassified. Originally thought to be a SMA type 1 (SMA1) cell line but shown to be from a SMA type 2 (SMA2) (PubMed=28284873)..
Proper citation: RRID:CVCL_F172 Copy
https://web.expasy.org/cellosaurus/CVCL_X110
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XY,del(7)(pter->q34) (Coriell=GM03733)., Population: Caucasian.
Proper citation: RRID:CVCL_X110 Copy
https://web.expasy.org/cellosaurus/CVCL_5M85
Organism: Homo sapiens (Human)
Disease: Duchenne muscular dystrophy
Category: Transformed cell line
Comments: Population: Caucasian; Iberian., Part of: Genetic Testing Reference Material (GeT-RM) samples.
Proper citation: RRID:CVCL_5M85 Copy
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