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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_CZ08
Organism: Homo sapiens (Human)
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM02979, RRID:CVCL_CZ08 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_5M81
Organism: Homo sapiens (Human)
Disease: Sporadic retinoblastoma
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;13)(p22jq12) (PubMed=10377420)., Population: Caucasian.
Proper citation: Coriell Cat# GM02971, RRID:CVCL_5M81 Copy
https://web.expasy.org/cellosaurus/CVCL_AX00
Organism: Homo sapiens (Human)
Disease: Leri-Weill dyschondrosteosis
Category: Finite cell line
Comments: Population: Caucasian; French.
Proper citation: Coriell Cat# GM02885, RRID:CVCL_AX00 Copy
https://web.expasy.org/cellosaurus/CVCL_DD73
Organism: Homo sapiens (Human)
Disease: Osteogenesis imperfecta
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM02962, RRID:CVCL_DD73 Copy
https://web.expasy.org/cellosaurus/CVCL_H962
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;3)(Xpter->Xq28::3q21->3qter;3pter->3q21::Xq28->Xqter) (Coriell=GM02899)., Population: Caucasian; Finnish.
Proper citation: Coriell Cat# GM02899, RRID:CVCL_H962 Copy
https://web.expasy.org/cellosaurus/CVCL_JX70
Organism: Homo sapiens (Human)
Disease: 5 alpha steroid reductase 2 deficiency
Category: Finite cell line
Comments: Population: Arab.
Proper citation: Coriell Cat# GM02935, RRID:CVCL_JX70 Copy
https://web.expasy.org/cellosaurus/CVCL_X097
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,rec(1)dup(q)ins(1)(pter->p22::q32->q31::p22->qter)pat (Coriell=GM02946)., Population: Caucasian.
Proper citation: Coriell Cat# GM02946, RRID:CVCL_X097 Copy
https://web.expasy.org/cellosaurus/CVCL_L755
Organism: Homo sapiens (Human)
Disease: Cockayne syndrome
Category: Transformed cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM02964, RRID:CVCL_L755 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_5M81
Organism: Homo sapiens (Human)
Disease: Sporadic retinoblastoma
Category: Finite cell line
Comments: Karyotypic information: 46,X,t(X;13)(p22jq12) (PubMed=10377420)., Population: Caucasian.
Proper citation: Coriell Cat# AG02971, RRID:CVCL_5M81 Copy
https://web.expasy.org/cellosaurus/CVCL_7374
Organism: Homo sapiens (Human)
Disease: Niemann-Pick disease, type C1
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: RRID:CVCL_7374 Copy
https://web.expasy.org/cellosaurus/CVCL_2S86
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(9;17)(9qter->9p22::17p11->17pter;17qter->17p11::9p22->9pter) (Coriell=GM03119)., Population: Caucasian.
Proper citation: RRID:CVCL_2S86 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_UR78
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: RRID:CVCL_UR78 Copy
Possibly Discontinued
https://web.expasy.org/cellosaurus/CVCL_X055
Organism: Homo sapiens (Human)
Category: Finite cell line
Proper citation: Coriell Cat# GM03121, RRID:CVCL_X055 Copy
https://web.expasy.org/cellosaurus/CVCL_4Z83
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian; Sardinian.
Proper citation: RRID:CVCL_4Z83 Copy
https://web.expasy.org/cellosaurus/CVCL_JE49
Organism: Homo sapiens (Human)
Disease: WAGR syndrome
Category: Finite cell line
Proper citation: RRID:CVCL_JE49 Copy
https://web.expasy.org/cellosaurus/CVCL_JM08
Organism: Homo sapiens (Human)
Disease: Anetoderma
Category: Finite cell line
Proper citation: RRID:CVCL_JM08 Copy
https://web.expasy.org/cellosaurus/CVCL_CW73
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Caucasian.
Proper citation: Coriell Cat# GM03074, RRID:CVCL_CW73 Copy
https://web.expasy.org/cellosaurus/CVCL_X102
Organism: Homo sapiens (Human)
Disease: Tetralogy of Fallot
Category: Finite cell line
Comments: Karyotypic information: 46,XX,der(1)(pter->p13.1::q21.1->p13.1::q21.1->q42.3) (Coriell=GM03126)., Population: African American.
Proper citation: RRID:CVCL_X102 Copy
https://web.expasy.org/cellosaurus/CVCL_X279
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Population: Puerto Rican.
Proper citation: Coriell Cat# GM03089, RRID:CVCL_X279 Copy
https://web.expasy.org/cellosaurus/CVCL_H190
Organism: Homo sapiens (Human)
Category: Finite cell line
Comments: Karyotypic information: 46,XX,t(9;17)(9qter->9p22::17p11->17pter;17qter->17p11::9p22->9pter)mat (Coriell=GM03100)., Population: Caucasian.
Proper citation: RRID:CVCL_H190 Copy
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