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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_8U31
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90012301, RRID:CVCL_8U31 Copy
https://web.expasy.org/cellosaurus/CVCL_8U39
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90060803, RRID:CVCL_8U39 Copy
https://web.expasy.org/cellosaurus/CVCL_E552
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Southeast Asian; Thai., Part of: 4th Asia-Oceania Histocompatibility Workshop (4AOHW) cell line panel.
Proper citation: ECACC Cat# 94082284, RRID:CVCL_E552 Copy
https://web.expasy.org/cellosaurus/CVCL_8U35
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90042701, RRID:CVCL_8U35 Copy
https://web.expasy.org/cellosaurus/CVCL_8U32
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90021605, RRID:CVCL_8U32 Copy
https://web.expasy.org/cellosaurus/CVCL_8U30
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XY,inv(6)(p21.33;q23.3),t(7;13) (ECACC=90010801)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90010801, RRID:CVCL_8U30 Copy
https://web.expasy.org/cellosaurus/CVCL_E556
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Southeast Asian; Thai., Part of: 4th Asia-Oceania Histocompatibility Workshop (4AOHW) cell line panel.
Proper citation: ECACC Cat# 94082286, RRID:CVCL_E556 Copy
https://web.expasy.org/cellosaurus/CVCL_E558
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Southeast Asian; Thai., Part of: 4th Asia-Oceania Histocompatibility Workshop (4AOHW) cell line panel.
Proper citation: ECACC Cat# 94082287, RRID:CVCL_E558 Copy
https://web.expasy.org/cellosaurus/CVCL_E551
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Population: Southeast Asian; Thai., Part of: 4th Asia-Oceania Histocompatibility Workshop (4AOHW) cell line panel.
Proper citation: ECACC Cat# 94082283, RRID:CVCL_E551 Copy
https://web.expasy.org/cellosaurus/CVCL_8U72
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XY,19q+mat (ECACC=88052403)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 88052403, RRID:CVCL_8U72 Copy
https://web.expasy.org/cellosaurus/CVCL_8U88
Organism: Homo sapiens (Human)
Disease: Angelman syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 91011609, RRID:CVCL_8U88 Copy
https://web.expasy.org/cellosaurus/CVCL_8U84
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 91011506, RRID:CVCL_8U84 Copy
https://web.expasy.org/cellosaurus/CVCL_8U58
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX; 47,XX,+18 (ECACC=90060402)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90060402, RRID:CVCL_8U58 Copy
https://web.expasy.org/cellosaurus/CVCL_8U55
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90090604, RRID:CVCL_8U55 Copy
https://web.expasy.org/cellosaurus/CVCL_8U51
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90110201, RRID:CVCL_8U51 Copy
https://web.expasy.org/cellosaurus/CVCL_8U59
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX; 47,XX,+mar mat (ECACC=90042503)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 90042503, RRID:CVCL_8U59 Copy
https://web.expasy.org/cellosaurus/CVCL_8U66
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 89070501, RRID:CVCL_8U66 Copy
https://web.expasy.org/cellosaurus/CVCL_8U73
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 47,XX,+dic(15)(pter->q11::q11->pter) (ECACC=870424011)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 870424011, RRID:CVCL_8U73 Copy
https://web.expasy.org/cellosaurus/CVCL_8U69
Organism: Homo sapiens (Human)
Disease: Fragile X syndrome
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 89021601, RRID:CVCL_8U69 Copy
https://web.expasy.org/cellosaurus/CVCL_8U68
Organism: Homo sapiens (Human)
Disease: Methylmalonic acidemia
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 89031702, RRID:CVCL_8U68 Copy
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