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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM03859 Resource Report Resource Website |
RRID:CVCL_W028 | Homo sapiens (Human) | Hypophosphatasia | Population: Caucasian. |
PMID:1409720 PMID:2705456 PMID:8675582 |
Finite cell line | Female | GM 3859, GM3859 | CLO:CLO_0015728, BioSample:SAMN00808571, Coriell:GM03859, Wikidata:Q54838275 |
CVCL_W028 | 2026-09-12 05:32:33 | 0 | ||||
|
GM03862 Resource Report Resource Website |
RRID:CVCL_1H67 | Homo sapiens (Human) | Huntington's disease | Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. | Finite cell line | Female | CLO:CLO_0015731, BioSample:SAMN00808574, Coriell:GM03862, Wikidata:Q54838281 |
CVCL_1H67 | 2026-09-12 05:32:33 | 0 | ||||||
|
GM03883 Resource Report Resource Website |
RRID:CVCL_X112 | Homo sapiens (Human) | Karyotypic information: 46,XX,inv(5)(q15;q33)pat.arr(1-22,X)x2 (Coriell=GM03883)., Population: Caucasian. |
PMID:6617268 PMID:23665875 |
Finite cell line | Female | GM 3883 | CLO:CLO_0016013, BioSample:SAMN00808590, Coriell:GM03883, Wikidata:Q54838298 |
CVCL_X112 | 2026-09-12 05:32:34 | 0 | |||||
|
GM03903 Resource Report Resource Website |
RRID:CVCL_IN20 | Homo sapiens (Human) | Neuropathy, hereditary sensory and autonomic, type IV | Population: Ecuadorian. | Finite cell line | Male | CLO:CLO_0015978, Coriell:GM03903, Wikidata:Q54838312 |
CVCL_IN20 | 2026-09-12 05:32:34 | 0 | ||||||
|
GM03868 Resource Report Resource Website 1+ mentions |
RRID:CVCL_1H73 | Homo sapiens (Human) | Huntington's disease | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0016025, BioSample:SAMN00808580, Coriell:GM03868, Wikidata:Q54838287 |
CVCL_1H73 | 2026-09-12 05:32:34 | 1 | ||||||
|
GM03907 Resource Report Resource Website |
RRID:CVCL_AK93 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian. | PMID:6726265 | Transformed cell line | Male | GM 3907, GM03907A | CLO:CLO_0015994, Coriell:GM03907, Wikidata:Q54838316 |
CVCL_AK93 | 2026-09-12 05:32:34 | 0 | ||||
|
GM03872 Resource Report Resource Website |
RRID:CVCL_1H77 | Homo sapiens (Human) | Huntington's disease | Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. | Finite cell line | Male | CLO:CLO_0016031, BioSample:SAMN00808584, Coriell:GM03872, Wikidata:Q54838291 |
CVCL_1H77 | 2026-09-12 05:32:34 | 0 | ||||||
|
GM03870 Resource Report Resource Website |
Coriell Cat# GM03870, RRID:CVCL_1H75 | Homo sapiens (Human) | Population: Caucasian. | Finite cell line | Female | GM03870A | Coriell | GM03870 | CLO:CLO_0016028, BioSample:SAMN00808582, Coriell:GM03870, Wikidata:Q54838289 |
CVCL_1H75 | 2026-09-12 05:32:34 | 0 | ||||
|
GM03850 Resource Report Resource Website |
RRID:CVCL_AM66 | Homo sapiens (Human) | Ehlers-Danlos syndrome | Population: Caucasian. | PMID:7094393 | Finite cell line | Female | GM3850 | CLO:CLO_0015631, BioSample:SAMN00808564, Coriell:GM03850, Wikidata:Q54838268 |
CVCL_AM66 | 2026-09-12 05:32:33 | 0 | ||||
|
GM03862 Resource Report Resource Website |
Coriell Cat# GM03862, RRID:CVCL_1H67 | Homo sapiens (Human) | Huntington's disease | Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. | Finite cell line | Female | Coriell | GM03862 | CLO:CLO_0015731, BioSample:SAMN00808574, Coriell:GM03862, Wikidata:Q54838281 |
CVCL_1H67 | 2026-09-12 05:32:33 | 0 | ||||
|
GM03857 Resource Report Resource Website |
Coriell Cat# GM03857, RRID:CVCL_DD75 | Homo sapiens (Human) | Hereditary optic atrophy | Population: Jewish. | Transformed cell line | Male | GM3857, GM03857A | Coriell | GM03857 | CLO:CLO_0015618, BioSample:SAMN00808569, Coriell:GM03857, Wikidata:Q54838273 |
CVCL_DD75 | 2026-09-12 05:32:33 | 0 | |||
|
GM03884 Resource Report Resource Website |
Coriell Cat# GM03884, RRID:CVCL_1N62 | Homo sapiens (Human) | Klippel-Feil syndrome | Karyotypic information: 46,X,t(X;16)(q26;q24) (PubMed=10377420)., Population: Caucasian. |
PMID:2498246 PMID:3495225 PMID:10377420 PMID:23665875 |
Finite cell line | Female | GM 3884, GM3884 | Coriell | GM03884 | CLO:CLO_0016011, BioSample:SAMN00808591, Coriell:GM03884, Wikidata:Q54838299 |
CVCL_1N62 | 2026-09-12 05:32:34 | 0 | ||
|
GM03890 Resource Report Resource Website |
Coriell Cat# GM03890, RRID:CVCL_W304 | Homo sapiens (Human) | Usher syndrome type 1 | Population: Caucasian. | Transformed cell line | Male | GM03890A | Coriell | GM03890 | CLO:CLO_0016007, BioSample:SAMN00808595, Coriell:GM03890, Wikidata:Q54838303 |
CVCL_W304 | 2026-09-12 05:32:34 | 0 | |||
|
GM03873 Resource Report Resource Website |
Coriell Cat# GM03873, RRID:CVCL_1H78 | Homo sapiens (Human) | Huntington's disease | Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. | Transformed cell line | Male | Coriell | GM03873 | CLO:CLO_0016033, BioSample:SAMN00808585, Coriell:GM03873, Wikidata:Q54838292 |
CVCL_1H78 | 2026-09-12 05:32:34 | 0 | ||||
|
GM03854 Resource Report Resource Website |
Coriell Cat# GM03854, RRID:CVCL_W308 | Homo sapiens (Human) | Usher syndrome type 1 | Population: Caucasian; German. | PMID:6726265 | Finite cell line | Male | GM 3854 | Coriell | GM03854 | CLO:CLO_0015626, BioSample:SAMN00808568, Coriell:GM03854, Wikidata:Q54838272 |
CVCL_W308 | 2026-09-12 05:32:33 | 0 | ||
|
GM03907 Resource Report Resource Website |
Coriell Cat# GM03907, RRID:CVCL_AK93 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian. | PMID:6726265 | Transformed cell line | Male | GM 3907, GM03907A | Coriell | GM03907 | CLO:CLO_0015994, Coriell:GM03907, Wikidata:Q54838316 |
CVCL_AK93 | 2026-09-12 05:32:34 | 0 | ||
|
GM03905 Resource Report Resource Website |
RRID:CVCL_K000 | Bos taurus (Bovine) | Senescence: Estimated life-span is ~80 PDL (PubMed=7355268). |
PMID:2112341 PMID:6833405 PMID:7355268 |
Finite cell line | Male | GM 3905, GM03905A, BFA-1c | CLO:CLO_0015981, Coriell:GM03905, Wikidata:Q54838314 |
CVCL_K000 | 2026-09-12 05:32:34 | 0 | |||||
|
GM03867 Resource Report Resource Website |
RRID:CVCL_1H72 | Homo sapiens (Human) | Huntington's disease | Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. | Transformed cell line | Female | CLO:CLO_0015709, BioSample:SAMN00808579, Coriell:GM03867, Wikidata:Q54838286 |
CVCL_1H72 | 2026-09-12 05:32:34 | 0 | ||||||
|
GM03905 Resource Report Resource Website |
Coriell Cat# GM03905, RRID:CVCL_K000 | Bos taurus (Bovine) | Senescence: Estimated life-span is ~80 PDL (PubMed=7355268). |
PMID:2112341 PMID:6833405 PMID:7355268 |
Finite cell line | Male | GM 3905, GM03905A, BFA-1c | Coriell | GM03905 | CLO:CLO_0015981, Coriell:GM03905, Wikidata:Q54838314 |
CVCL_K000 | 2026-09-12 05:32:34 | 0 | |||
|
GM03910 Resource Report Resource Website |
RRID:CVCL_AK94 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0015996, Coriell:GM03910, Wikidata:Q54838317 |
CVCL_AK94 | 2026-09-12 05:32:34 | 0 |
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