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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_9J94
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 95080202, RRID:CVCL_9J94 Copy
https://web.expasy.org/cellosaurus/CVCL_9J95
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 95080801, RRID:CVCL_9J95 Copy
https://web.expasy.org/cellosaurus/CVCL_AR03
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 95101713, RRID:CVCL_AR03 Copy
https://web.expasy.org/cellosaurus/CVCL_9J87
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 95063112, RRID:CVCL_9J87 Copy
https://web.expasy.org/cellosaurus/CVCL_9K05
Organism: Homo sapiens (Human)
Disease:
Category: Transformed cell line
Comments: Karyotypic information: 46,XX,ins(7)(q42.1;q34.1;q35) (ECACC=95102509)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 95102509, RRID:CVCL_9K05 Copy
https://web.expasy.org/cellosaurus/CVCL_9J74
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 95062313, RRID:CVCL_9J74 Copy
https://web.expasy.org/cellosaurus/CVCL_9J89
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,var(6)cen (ECACC=95063016)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 95063016, RRID:CVCL_9J89 Copy
https://web.expasy.org/cellosaurus/CVCL_9J84
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX; 47,XX,+10 (ECACC=95062822)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 95062822, RRID:CVCL_9J84 Copy
https://web.expasy.org/cellosaurus/CVCL_9J97
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 95082410, RRID:CVCL_9J97 Copy
https://web.expasy.org/cellosaurus/CVCL_9J72
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 95062310, RRID:CVCL_9J72 Copy
https://web.expasy.org/cellosaurus/CVCL_9J79
Organism: Homo sapiens (Human)
Disease: Neurofibromatosis type 1
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 95062708, RRID:CVCL_9J79 Copy
https://web.expasy.org/cellosaurus/CVCL_9J91
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 95070103, RRID:CVCL_9J91 Copy
https://web.expasy.org/cellosaurus/CVCL_9J66
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 95061635, RRID:CVCL_9J66 Copy
https://web.expasy.org/cellosaurus/CVCL_9K03
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 95092606, RRID:CVCL_9K03 Copy
https://web.expasy.org/cellosaurus/CVCL_AQ97
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 95062311, RRID:CVCL_AQ97 Copy
https://web.expasy.org/cellosaurus/CVCL_9K37
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 96022310, RRID:CVCL_9K37 Copy
https://web.expasy.org/cellosaurus/CVCL_9K28
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 96012910, RRID:CVCL_9K28 Copy
https://web.expasy.org/cellosaurus/CVCL_9K35
Organism: Homo sapiens (Human)
Disease: Turner syndrome
Category: Transformed cell line
Comments: Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 96022001, RRID:CVCL_9K35 Copy
https://web.expasy.org/cellosaurus/CVCL_9K36
Organism: Homo sapiens (Human)
Disease:
Category: Finite cell line
Comments: Karyotypic information: 46,XX,der(4),t(4;9) (ECACC=96022101)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 96022101, RRID:CVCL_9K36 Copy
https://web.expasy.org/cellosaurus/CVCL_9K50
Organism: Homo sapiens (Human)
Disease: Smith-Lemli-Opitz syndrome
Category: Finite cell line
Comments: Karyotypic information: 46,XY.ish 22q11-2(cH748x2) (ECACC=96050810)., Part of: ECACC chromosomal abnormality collection.
Proper citation: ECACC Cat# 96050810, RRID:CVCL_9K50 Copy
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