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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM11337 Resource Report Resource Website |
RRID:CVCL_W638 | Homo sapiens (Human) | 47,XYY syndrome | Karyotypic information: 47,XYY (Coriell=GM11337)., Population: Caucasian. | Finite cell line | Male | CLO:CLO_0026063, Coriell:GM11337, Wikidata:Q54845019 |
CVCL_W638 | 2026-09-12 05:34:14 | 0 | ||||||
|
GM11370 Resource Report Resource Website |
RRID:CVCL_0N11 | Homo sapiens (Human) | Cystic fibrosis | Part of: Genetic Testing Reference Material (GeT-RM) samples. | PMID:19359498 | Transformed cell line | Male | CLO:CLO_0026074, Coriell:GM11370, Wikidata:Q54845037 |
CVCL_0N11 | 2026-09-12 05:34:14 | 0 | |||||
|
GM11388 Resource Report Resource Website |
RRID:CVCL_U533 | Homo sapiens (Human) | Prader-Willi syndrome | PMID:23665875 | Transformed cell line | Male | CLO:CLO_0026083, Coriell:GM11388, Wikidata:Q54845048 |
CVCL_U533 | 2026-09-12 05:34:15 | 0 | ||||||
|
GM11424 Resource Report Resource Website |
RRID:CVCL_L747 | Homo sapiens (Human) | Population: Caucasian. | Transformed cell line | Female | CLO:CLO_0020876, Coriell:GM11424, Wikidata:Q54845084 |
CVCL_L747 | 2026-09-12 05:34:15 | 0 | |||||||
|
GM11397 Resource Report Resource Website |
RRID:CVCL_2U07 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(8;10)(8qter->8p11.2::10q24->10qter;10pter->10q24::8p11.2->8pter) (Coriell=GM11397). | Finite cell line | Female | CLO:CLO_0026095, Coriell:GM11397, Wikidata:Q54845055 |
CVCL_2U07 | 2026-09-12 05:34:15 | 0 | |||||||
|
GM11404 Resource Report Resource Website |
RRID:CVCL_5P52 | Homo sapiens (Human) | Angelman syndrome | PMID:23665875 | Transformed cell line | Male | CLO:CLO_0026093, BioSample:SAMN00800623, Coriell:GM11404, Wikidata:Q54845060 |
CVCL_5P52 | 2026-09-12 05:34:15 | 0 | ||||||
|
GM11392 Resource Report Resource Website |
RRID:CVCL_5P49 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | CLO:CLO_0026090, Coriell:GM11392, Wikidata:Q54845052 |
CVCL_5P49 | 2026-09-12 05:34:15 | 0 | |||||||
|
GM11432 Resource Report Resource Website |
RRID:CVCL_6E35 | Homo sapiens (Human) | PMID:1850193 | Transformed cell line | Female | C5807 pSVori- transformed clone 7 | CLO:CLO_0020861, Coriell:GM11432, Wikidata:Q54845091 |
CVCL_6E35 | 2026-09-12 05:34:15 | 0 | ||||||
|
GM11386 Resource Report Resource Website |
RRID:CVCL_5P45 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | CLO:CLO_0026085, Coriell:GM11386, Wikidata:Q54845046 |
CVCL_5P45 | 2026-09-12 05:34:14 | 0 | |||||||
|
GM11374 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM11374, RRID:CVCL_UW17 | Homo sapiens (Human) | Population: Southeast Asian; Khmer Cambodian., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel. | Transformed cell line | Male | 86-171 | Coriell | GM11374 | Coriell:GM11374, Wikidata:Q93815030 |
CVCL_UW17 | 2026-09-12 05:34:14 | 0 | ||||
|
GM11418 Resource Report Resource Website |
RRID:CVCL_1S24 | Cricetulus griseus (Chinese hamster) | Characteristics: Hybrid for chromosome 15 mapping. Contains a complete copy of chromosome 15., Group: Human/rodent somatic cell hybrid. | PMID:8314568 | Hybrid cell line | 15A | CLO:CLO_0020792, Coriell:GM11418, Wikidata:Q54845072 |
cvcl_0214 | CVCL_1S24 | 2026-09-12 05:34:15 | 0 | |||||
|
GM11391 Resource Report Resource Website |
RRID:CVCL_U534 | Homo sapiens (Human) | Prader-Willi syndrome | PMID:23665875 | Transformed cell line | Male | CLO:CLO_0026089, Coriell:GM11391, Wikidata:Q54845051 |
CVCL_U534 | 2026-09-12 05:34:15 | 0 | ||||||
|
GM11377 Resource Report Resource Website |
Coriell Cat# GM17088, RRID:CVCL_N177 | Homo sapiens (Human) | Population: Southeast Asian; Khmer Cambodian., Part of: Yale-Stanford Collection from NIGMS Human Genetic Cell Repository., Part of: Human variation panel. | PMID:14583597 | Transformed cell line | Male | GM17088, 86-194 | Coriell | GM17088 | CLO:CLO_0014488, CLO:CLO_0026077, Coriell:GM11377, Coriell:GM17088, Wikidata:Q54845040 |
CVCL_N177 | 2026-09-12 05:34:14 | 0 | |||
|
GM11420 Resource Report Resource Website |
Coriell Cat# GM11420, RRID:CVCL_N183 | Homo sapiens (Human) | Karyotypic information: 49,XYYYY (Coriell=GM11420)., Population: Indian (from Guyana). | Finite cell line | Male | Coriell | GM11420 | CLO:CLO_0020868, Coriell:GM11420, Wikidata:Q54845082 |
CVCL_N183 | 2026-09-12 05:34:15 | 0 | |||||
|
GM11503 Resource Report Resource Website |
Coriell Cat# GM11503, RRID:CVCL_AV56 | Homo sapiens (Human) | Population: Caucasian; English/German. | Transformed cell line | Female | GM11503A | Coriell | GM11503 | CLO:CLO_0020952, Coriell:GM11503, Wikidata:Q54845120 |
CVCL_AV56 | 2026-09-12 05:34:16 | 0 | ||||
|
GM11529 Resource Report Resource Website |
Coriell Cat# GM11529, RRID:CVCL_Y575 | Homo sapiens (Human) | Infantile neuroaxonal dystrophy | Population: Hispanic. | Finite cell line | Male | Coriell | GM11529 | CLO:CLO_0021003, Coriell:GM11529, Wikidata:Q54845141 |
CVCL_Y575 | 2026-09-12 05:34:17 | 0 | ||||
|
GM11526 Resource Report Resource Website |
RRID:CVCL_DE46 | Homo sapiens (Human) | Group: Human/rodent somatic cell hybrid. | Hybrid cell line | GM11526A, A9/1492-37 | CLO:CLO_0021033, Coriell:GM11526, Wikidata:Q54845140 |
cvcl_3984 | CVCL_DE46 | 2026-09-12 05:34:17 | 0 | ||||||
|
GM11492 Resource Report Resource Website |
RRID:CVCL_4I72 | Homo sapiens (Human) | Population: Caucasian; Amish., Part of: Old Order Amish Major Affective Disorder cell line collection. | Transformed cell line | Male | GM11492A | CLO:CLO_0020982, Coriell:GM11492, Wikidata:Q54845110 |
CVCL_4I72 | 2026-09-12 05:34:16 | 0 | ||||||
|
GM11554 Resource Report Resource Website |
RRID:CVCL_JF46 | Homo sapiens (Human) | Familial hemophagocytic lymphohistiocytosis | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0021053, Coriell:GM11554, Wikidata:Q54845154 |
CVCL_JF46 | 2026-09-12 05:34:17 | 0 | ||||||
|
GM11457 Resource Report Resource Website |
RRID:CVCL_AJ56 | Homo sapiens (Human) | Population: Caucasian., Part of: R-W pedigree MODY cell line collection. | PMID:8945471 | Transformed cell line | Female | CLO:CLO_0020881, Coriell:GM11457, Wikidata:Q54845096 |
CVCL_AJ56 | 2026-09-12 05:34:16 | 0 |
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