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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM09329 Resource Report Resource Website |
RRID:CVCL_8A12 | Homo sapiens (Human) | Tourette syndrome | Transformed cell line | Female | CLO:CLO_0011908, Coriell:GM09329, Wikidata:Q54843680 |
CVCL_8A12 | 2026-07-25 04:34:04 | 0 | |||||||
|
GM09301 Resource Report Resource Website |
RRID:CVCL_N104 | Homo sapiens (Human) | Population: Jewish; Ashkenazi., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. |
PMID:20889555 PMID:29959025 |
Transformed cell line | Male | GM17365 | CLO:CLO_0011876, CLO:CLO_0013708, Coriell:GM09301, Coriell:GM17365, Wikidata:Q54843661 |
CVCL_N104 | 2026-07-25 04:34:04 | 0 | |||||
|
GM09297 Resource Report Resource Website |
RRID:CVCL_AA75 | Homo sapiens (Human) | Familial dysautonomia | Population: Jewish; Ashkenazi. | Transformed cell line | Male | CLO:CLO_0011884, Coriell:GM09297, Wikidata:Q54843657 |
CVCL_AA75 | 2026-07-25 04:34:04 | 0 | ||||||
|
GM09303 Resource Report Resource Website |
Coriell Cat# GM09303, RRID:CVCL_8A08 | Homo sapiens (Human) | Transformed cell line | Male | Coriell | GM09303 | CLO:CLO_0011878, Coriell:GM09303, Wikidata:Q54843663 |
CVCL_8A08 | 2026-07-25 04:34:04 | 0 | ||||||
|
GM09325 Resource Report Resource Website |
RRID:CVCL_CZ26 | Homo sapiens (Human) | Finite cell line | Male | CLO:CLO_0011910, Coriell:GM09325, Wikidata:Q54843678 |
CVCL_CZ26 | 2026-07-25 04:34:05 | 0 | ||||||||
|
GM09291 Resource Report Resource Website |
Coriell Cat# GM09291, RRID:CVCL_9X08 | Homo sapiens (Human) | Rhizomelic chondrodysplasia punctata | Population: Caucasian. | Transformed cell line | Male | Coriell | GM09291 | CLO:CLO_0012044, Coriell:GM09291, Wikidata:Q54843650 |
CVCL_9X08 | 2026-07-25 04:34:03 | 0 | ||||
|
GM09302 Resource Report Resource Website |
RRID:CVCL_AA79 | Homo sapiens (Human) | Population: Jewish; Ashkenazi. | Transformed cell line | Female | CLO:CLO_0011875, Coriell:GM09302, Wikidata:Q54843662 |
CVCL_AA79 | 2026-07-25 04:34:04 | 0 | |||||||
|
GM09297 Resource Report Resource Website |
Coriell Cat# GM09297, RRID:CVCL_AA75 | Homo sapiens (Human) | Familial dysautonomia | Population: Jewish; Ashkenazi. | Transformed cell line | Male | Coriell | GM09297 | CLO:CLO_0011884, Coriell:GM09297, Wikidata:Q54843657 |
CVCL_AA75 | 2026-07-25 04:34:05 | 0 | ||||
|
GM09294 Resource Report Resource Website |
Coriell Cat# GM09294, RRID:CVCL_AA72 | Homo sapiens (Human) | Population: Jewish; Ashkenazi. | Transformed cell line | Female | Coriell | GM09294 | CLO:CLO_0011880, Coriell:GM09294, Wikidata:Q54843653 |
CVCL_AA72 | 2026-07-25 04:34:03 | 0 | |||||
|
GM09354 Resource Report Resource Website |
Coriell Cat# GM09354, RRID:CVCL_5L84 | Homo sapiens (Human) | Transformed cell line | Female | Coriell | GM09354 | CLO:CLO_0011974, Coriell:GM09354, Wikidata:Q54843699 |
CVCL_5L84 | 2026-07-25 04:34:06 | 0 | ||||||
|
GM09331 Resource Report Resource Website |
Coriell Cat# GM09331, RRID:CVCL_8A14 | Homo sapiens (Human) | Transformed cell line | Female | Coriell | GM09331 | CLO:CLO_0011947, Coriell:GM09331, Wikidata:Q54843682 |
CVCL_8A14 | 2026-07-25 04:34:05 | 0 | ||||||
|
GM09354 Resource Report Resource Website |
RRID:CVCL_5L84 | Homo sapiens (Human) | Transformed cell line | Female | CLO:CLO_0011974, Coriell:GM09354, Wikidata:Q54843699 |
CVCL_5L84 | 2026-07-25 04:34:04 | 0 | ||||||||
|
GM09326 Resource Report Resource Website |
RRID:CVCL_W637 | Homo sapiens (Human) | 47,XYY syndrome | Karyotypic information: 47,XYY (Coriell=GM09326)., Population: Caucasian; English/Irish. | Finite cell line | Male | CLO:CLO_0011909, Coriell:GM09326, Wikidata:Q54843679 |
CVCL_W637 | 2026-07-25 04:34:04 | 0 | ||||||
|
GM09311 Resource Report Resource Website |
RRID:CVCL_8A11 | Homo sapiens (Human) | Tourette syndrome | Transformed cell line | Male | CLO:CLO_0011907, Coriell:GM09311, Wikidata:Q54843669 |
CVCL_8A11 | 2026-07-25 04:34:04 | 0 | |||||||
|
GM09335 Resource Report Resource Website |
RRID:CVCL_5L71 | Homo sapiens (Human) | Tuberous sclerosis 2 | Transformed cell line | Male | CLO:CLO_0011941, Coriell:GM09335, Wikidata:Q54843685 |
CVCL_5L71 | 2026-07-25 04:34:04 | 0 | |||||||
|
GM09290 Resource Report Resource Website |
RRID:CVCL_2T63 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(1;6)(1pter->1q43::6q23->6qter;6pter->6q23::1q43->1qter) (Coriell=GM09290)., Population: Caucasian. | Finite cell line | Female | GM09290A | CLO:CLO_0012043, Coriell:GM09290, Wikidata:Q54843649 |
CVCL_2T63 | 2026-07-25 04:34:03 | 0 | ||||||
|
GM09287 Resource Report Resource Website |
RRID:CVCL_9S93 | Homo sapiens (Human) | Trisomy 9 | Karyotypic information: 47,XY,+9 (Coriell=GM09287)., Population: African American. | Finite cell line | Male | CLO:CLO_0012045, Coriell:GM09287, Wikidata:Q54843648 |
CVCL_9S93 | 2026-07-25 04:34:04 | 0 | ||||||
|
GM09301 Resource Report Resource Website |
Coriell Cat# GM17365, RRID:CVCL_N104 | Homo sapiens (Human) | Population: Jewish; Ashkenazi., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. |
PMID:20889555 PMID:29959025 |
Transformed cell line | Male | GM17365 | Coriell | GM17365 | CLO:CLO_0011876, CLO:CLO_0013708, Coriell:GM09301, Coriell:GM17365, Wikidata:Q54843661 |
CVCL_N104 | 2026-07-25 04:34:05 | 0 | |||
|
GM09317 Resource Report Resource Website |
RRID:CVCL_AY33 | Homo sapiens (Human) | Fragile X syndrome | PMID:1672039 | Transformed cell line | Male | GM9317 | CLO:CLO_0011905, Coriell:GM09317, Wikidata:Q54843676 |
CVCL_AY33 | 2026-07-25 04:34:04 | 0 | |||||
|
GM09282 Resource Report Resource Website |
Coriell Cat# GM09282, RRID:CVCL_1K61 | Homo sapiens (Human) | Glycogen storage disease type II | PMID:1652892 | Transformed cell line | Female | GM 9282 | Coriell | GM09282 | CLO:CLO_0012060, Coriell:GM09282, Wikidata:Q54843642 |
CVCL_1K61 | 2026-07-25 04:34:03 | 0 |
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