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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM03794 Resource Report Resource Website |
RRID:CVCL_F078 | Homo sapiens (Human) | Huntington's disease | Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease. | Transformed cell line | Female | CLO:CLO_0015574, BioSample:SAMN00808537, Coriell:GM03794, Wikidata:Q54838241 |
CVCL_F078 | 2026-09-12 05:32:32 | 0 | ||||||
|
GM03769 Resource Report Resource Website |
Coriell Cat# GM03769, RRID:CVCL_X299 | Homo sapiens (Human) | Trisomy 18 | PMID:6661932 | Finite cell line | Male | GM 3769 | Coriell | GM03769 | CLO:CLO_0015492, BioSample:SAMN00808522, Coriell:GM03769, Wikidata:Q54838224 |
CVCL_X299 | 2026-09-12 05:32:32 | 0 | |||
|
GM03834 Resource Report Resource Website |
Coriell Cat# GM03834, RRID:CVCL_AK85 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian. | PMID:6726265 | Transformed cell line | Female | GM 3834, GM03834A | Coriell | GM03834 | CLO:CLO_0015666, BioSample:SAMN00808558, Coriell:GM03834, Wikidata:Q54838262 |
CVCL_AK85 | 2026-09-12 05:32:33 | 0 | ||
|
GM03781 Resource Report Resource Website |
RRID:CVCL_M943 | Homo sapiens (Human) | Duchenne muscular dystrophy | Population: Caucasian; Iberian. |
PMID:3863481 PMID:23665875 |
Finite cell line | Male | GM 3781, GM3781 | CLO:CLO_0015501, BioSample:SAMN00808529, Coriell:GM03781, Wikidata:Q54838231 |
CVCL_M943 | 2026-09-12 05:32:32 | 0 | ||||
|
GM03798 Resource Report Resource Website |
Coriell Cat# GM03798, RRID:CVCL_7403 | Homo sapiens (Human) | Population: Caucasian. |
PMID:16260726 PMID:18485778 PMID:19127062 |
Transformed cell line | Male | GM03798A | Coriell | GM03798 | CLO:CLO_0015579, BioSample:SAMN00808539, Coriell:GM03798, Wikidata:Q54838243 |
CVCL_7403 | 2026-09-12 05:32:32 | 0 | |||
|
GM03770 Resource Report Resource Website |
RRID:CVCL_U395 | Homo sapiens (Human) | Tay-Sachs disease | Part of: Genetic Testing Reference Material (GeT-RM) samples. | PMID:19815695 | Transformed cell line | Male | CLO:CLO_0015504, BioSample:SAMN00808523, Coriell:GM03770, Wikidata:Q54838225 |
CVCL_U395 | 2026-09-12 05:32:32 | 0 | |||||
|
GM03733 Resource Report Resource Website |
Coriell Cat# GM03733, RRID:CVCL_X110 | Homo sapiens (Human) | Karyotypic information: 46,XY,del(7)(pter->q34) (Coriell=GM03733)., Population: Caucasian. |
PMID:6617268 PMID:6661932 |
Finite cell line | Male | GM-3733, GM 3733 | Coriell | GM03733 | CLO:CLO_0015525, BioSample:SAMN00808514, Coriell:GM03733, Wikidata:Q54838213 |
CVCL_X110 | 2026-09-12 05:32:32 | 0 | |||
|
GM03784 Resource Report Resource Website |
RRID:CVCL_DF22 | Homo sapiens (Human) | Macular dystrophy, retinal, 1 | Transformed cell line | Male | CLO:CLO_0015604, BioSample:SAMN00808532, Coriell:GM03784, Wikidata:Q54838234 |
CVCL_DF22 | 2026-09-12 05:32:32 | 0 | |||||||
|
GM03793 Resource Report Resource Website |
Coriell Cat# GM03793, RRID:CVCL_F077 | Homo sapiens (Human) | Huntington's disease | Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease. | Finite cell line | Female | Coriell | GM03793 | CLO:CLO_0015571, BioSample:SAMN00808536, Coriell:GM03793, Wikidata:Q54838240 |
CVCL_F077 | 2026-09-12 05:32:32 | 0 | ||||
|
GM03824 Resource Report Resource Website |
RRID:CVCL_AK79 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian; German. | Finite cell line | Male | CLO:CLO_0015683, BioSample:SAMN00808550, Coriell:GM03824, Wikidata:Q54838254 |
CVCL_AK79 | 2026-09-12 05:32:33 | 0 | ||||||
|
GM03799 Resource Report Resource Website |
RRID:CVCL_2S94 | Homo sapiens (Human) | Transformed cell line | Female | CLO:CLO_0015547, BioSample:SAMN00808540, Coriell:GM03799, Wikidata:Q54838244 |
CVCL_2S94 | 2026-09-12 05:32:32 | 0 | ||||||||
|
GM03791 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM03791, RRID:CVCL_UR85 | Homo sapiens (Human) | Huntington's disease | Finite cell line | Male | Coriell | GM03791 | Coriell:GM03791, Wikidata:Q93585687 |
CVCL_UR85 | 2026-09-12 05:32:32 | 0 | |||||
|
GM03835 Resource Report Resource Website |
RRID:CVCL_AK86 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0015668, BioSample:SAMN00808559, Coriell:GM03835, Wikidata:Q54838263 |
CVCL_AK86 | 2026-09-12 05:32:33 | 0 | ||||||
|
GM03726 Resource Report Resource Website |
RRID:CVCL_9W96 | Homo sapiens (Human) | Population: African American. | Finite cell line | Female | CLO:CLO_0015527, BioSample:SAMN00808512, Coriell:GM03726, Wikidata:Q54838211 |
CVCL_9W96 | 2026-09-12 05:32:31 | 0 | |||||||
|
GM03831 Resource Report Resource Website |
RRID:CVCL_AK82 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0015674, BioSample:SAMN00808555, Coriell:GM03831, Wikidata:Q54838259 |
CVCL_AK82 | 2026-09-12 05:32:33 | 0 | ||||||
|
GM03793 Resource Report Resource Website |
RRID:CVCL_F077 | Homo sapiens (Human) | Huntington's disease | Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease. | Finite cell line | Female | CLO:CLO_0015571, BioSample:SAMN00808536, Coriell:GM03793, Wikidata:Q54838240 |
CVCL_F077 | 2026-09-12 05:32:32 | 0 | ||||||
|
GM03866 Resource Report Resource Website |
RRID:CVCL_1H71 | 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_0015710, BioSample:SAMN00808578, Coriell:GM03866, Wikidata:Q54838285 |
CVCL_1H71 | 2026-09-12 05:32:34 | 0 | ||||||
|
GM03876 Resource Report Resource Website |
Coriell Cat# GM03876, RRID:CVCL_1N78 | Homo sapiens (Human) | Karyotypic information: 46,XY,t(1;20)(1qter->1p13::20q13.3->20qter;20pter->20q13.3::1p13->1pter) (Coriell=GM03876)., Population: Caucasian. | PMID:2535035 | Finite cell line | Male | GM3876 | Coriell | GM03876 | CLO:CLO_0016034, BioSample:SAMN00808586, Coriell:GM03876, Wikidata:Q54838293 |
CVCL_1N78 | 2026-09-12 05:32:34 | 0 | |||
|
GM03894 Resource Report Resource Website |
RRID:CVCL_AK91 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian. | PMID:6726265 | Transformed cell line | Male | GM 3894 | CLO:CLO_0016018, BioSample:SAMN00808599, Coriell:GM03894, Wikidata:Q54838307 |
CVCL_AK91 | 2026-09-12 05:32:34 | 0 | ||||
|
GM03901 Resource Report Resource Website |
RRID:CVCL_X334 | Homo sapiens (Human) | Familial adenomatous polyposis | Population: African American. |
PMID:3374507 PMID:6617268 |
Finite cell line | Female | GM 3901, GM3901 | CLO:CLO_0015989, Coriell:GM03901, Wikidata:Q54838311 |
CVCL_X334 | 2026-09-12 05:32:34 | 0 |
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