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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.
| Name | Proper Citation | Organism | Disease |
Comments |
Defining Citation | Category | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM21261 Resource Report Resource Website |
RRID:CVCL_5U26 | Homo sapiens (Human) | Mayer-Rokitansky-Kuster-Hauser syndrome | PMID:23665875 | Transformed cell line | Female | CLO:CLO_0015823, Coriell:GM21261, Wikidata:Q54851757 |
CVCL_5U26 | 2026-02-14 08:19:56 | 0 | ||||||
|
GM21261 Resource Report Resource Website |
Coriell Cat# GM21261, RRID:CVCL_5U26 | Homo sapiens (Human) | Mayer-Rokitansky-Kuster-Hauser syndrome | PMID:23665875 | Transformed cell line | Female | Coriell | GM21261 | CLO:CLO_0015823, Coriell:GM21261, Wikidata:Q54851757 |
CVCL_5U26 | 2026-02-14 08:19:56 | 0 | ||||
|
GM21496 Resource Report Resource Website |
Coriell Cat# GM21496, RRID:CVCL_5U27 | Homo sapiens (Human) | Mayer-Rokitansky-Kuster-Hauser syndrome | PMID:23665875 | Transformed cell line | Male | Coriell | GM21496 | CLO:CLO_0014050, Coriell:GM21496, Wikidata:Q54851944 |
CVCL_5U27 | 2026-02-14 08:20:01 | 0 | ||||
|
GM21681 Resource Report Resource Website |
Coriell Cat# GM21681, RRID:CVCL_5R35 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | Coriell | GM21681 | Coriell:GM21681, Wikidata:Q54852080 |
CVCL_5R35 | 2026-02-14 08:20:04 | 0 | |||||
|
GM21715 Resource Report Resource Website |
RRID:CVCL_5R37 | Homo sapiens (Human) | Autism spectrum disorder | Population: African American. |
PMID:23495136 PMID:23665875 |
Transformed cell line | Male | 801-002 LCL | Coriell:GM21715, Wikidata:Q54852090 |
CVCL_5R37 | 2026-02-14 08:20:04 | 0 | ||||
|
GM21699 Resource Report Resource Website |
Coriell Cat# GM21699, RRID:CVCL_4J61 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | Coriell | GM21699 | CLO:CLO_0014010, Coriell:GM21699, Wikidata:Q54852089 |
CVCL_4J61 | 2026-02-14 08:20:04 | 0 | |||||
|
GM16808 Resource Report Resource Website |
RRID:CVCL_5Q79 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | Coriell:GM16808, Wikidata:Q54848755 |
CVCL_5Q79 | 2026-02-14 08:18:52 | 0 | |||||||
|
GM16810 Resource Report Resource Website |
Coriell Cat# GM16810, RRID:CVCL_5Q81 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | Coriell | GM16810 | Coriell:GM16810, Wikidata:Q54848757 |
CVCL_5Q81 | 2026-02-14 08:18:52 | 0 | |||||
|
GM17437 Resource Report Resource Website |
RRID:CVCL_4E15 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | CLO:CLO_0012909, Coriell:GM17437, Wikidata:Q54848874 |
CVCL_4E15 | 2026-02-14 08:18:53 | 0 | |||||||
|
GM17437 Resource Report Resource Website |
Coriell Cat# GM17437, RRID:CVCL_4E15 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | Coriell | GM17437 | CLO:CLO_0012909, Coriell:GM17437, Wikidata:Q54848874 |
CVCL_4E15 | 2026-02-14 08:18:53 | 0 | |||||
|
GM16994 Resource Report Resource Website |
Coriell Cat# GM16994, RRID:CVCL_2N34 | Homo sapiens (Human) | Autism spectrum disorder | PMID:23665875 | Transformed cell line | Male | Coriell | GM16994 | Coriell:GM16994, Wikidata:Q54848827 |
CVCL_2N34 | 2026-02-14 08:18:53 | 0 | ||||
|
GM17867 Resource Report Resource Website |
Coriell Cat# GM17867, RRID:CVCL_W965 | Homo sapiens (Human) | Klinefelter syndrome | PMID:23665875 | Transformed cell line | Male | Coriell | GM17867 | CLO:CLO_0016462, Coriell:GM17867, Wikidata:Q54849292 |
CVCL_W965 | 2026-02-14 08:19:01 | 0 | ||||
|
GM17938 Resource Report Resource Website |
Coriell Cat# GM17938, RRID:CVCL_5Q82 | Homo sapiens (Human) | 22q11.2 deletion syndrome | PMID:23665875 | Transformed cell line | Male | Coriell | GM17938 | CLO:CLO_0016282, Coriell:GM17938, Wikidata:Q54849337 |
CVCL_5Q82 | 2026-02-14 08:19:02 | 0 | ||||
|
GM17938 Resource Report Resource Website |
RRID:CVCL_5Q82 | Homo sapiens (Human) | 22q11.2 deletion syndrome | PMID:23665875 | Transformed cell line | Male | CLO:CLO_0016282, Coriell:GM17938, Wikidata:Q54849337 |
CVCL_5Q82 | 2026-02-14 08:19:02 | 0 | ||||||
|
GM21889 Resource Report Resource Website |
RRID:CVCL_U542 | Homo sapiens (Human) | Prader-Willi syndrome | Population: African American. |
PMID:23665875 PMID:24816254 |
Finite cell line | Male | Coriell:GM21889, Wikidata:Q54852210 |
CVCL_U542 | 2026-02-14 08:20:07 | 0 | |||||
|
GM21893 Resource Report Resource Website |
Coriell Cat# GM21893, RRID:CVCL_5R48 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | Coriell | GM21893 | Coriell:GM21893, Wikidata:Q54852214 |
CVCL_5R48 | 2026-02-14 08:20:07 | 0 | |||||
|
GM21878 Resource Report Resource Website |
RRID:CVCL_5R41 | Homo sapiens (Human) | PMID:23665875 | Finite cell line | Female | Coriell:GM21878, Wikidata:Q54852196 |
CVCL_5R41 | 2026-02-14 08:20:07 | 0 | |||||||
|
GM21890 Resource Report Resource Website |
Coriell Cat# GM21890, RRID:CVCL_U543 | Homo sapiens (Human) | Prader-Willi syndrome | PMID:23665875 | Finite cell line | Male | Coriell | GM21890 | Coriell:GM21890, Wikidata:Q54852211 |
CVCL_U543 | 2026-02-14 08:20:07 | 0 | ||||
|
GM21877 Resource Report Resource Website |
RRID:CVCL_F109 | Homo sapiens (Human) | PMID:23665875 | Finite cell line | Female | Coriell:GM21877, Wikidata:Q54852195 |
CVCL_F109 | 2026-02-14 08:20:07 | 0 | |||||||
|
GM21887 Resource Report Resource Website |
Coriell Cat# GM21887, RRID:CVCL_5R46 | Homo sapiens (Human) | Angelman syndrome | PMID:23665875 | Transformed cell line | Female | Coriell | GM21887 | Coriell:GM21887, Wikidata:Q54852209 |
CVCL_5R46 | 2026-02-14 08:20:07 | 0 |
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