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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM16599 Resource Report Resource Website |
RRID:CVCL_5Q75 | Cricetulus griseus (Chinese hamster) | Group: Human/rodent somatic cell hybrid. | PMID:7896290 | Hybrid cell line | JH164 | CLO:CLO_0017352, Coriell:GM16599, Wikidata:Q54848672 |
CVCL_5Q75 | 2026-09-05 10:58:03 | 0 | ||||||
|
GM16547 Resource Report Resource Website |
RRID:CVCL_4F41 | Homo sapiens (Human) | Rett syndrome | Transformed cell line | Female | CLO:CLO_0017558, Coriell:GM16547, Wikidata:Q54848633 |
CVCL_4F41 | 2026-09-05 10:58:03 | 0 | |||||||
|
GM16688 Resource Report Resource Website |
RRID:CVCL_AB37 | Homo sapiens (Human) | Population: Chinese., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. |
PMID:20889555 PMID:29959025 |
Transformed cell line | Female | CLO:CLO_0017468, Coriell:GM16688, Wikidata:Q54848701 |
CVCL_AB37 | 2026-09-05 10:58:04 | 0 | ||||||
|
GM16678 Resource Report Resource Website |
RRID:CVCL_9Y36 | Homo sapiens (Human) | Rhizomelic chondrodysplasia punctata | Population: Lebanese. | Finite cell line | Female | CLO:CLO_0017451, Coriell:GM16678, Wikidata:Q54848695 |
CVCL_9Y36 | 2026-09-05 10:58:04 | 0 | ||||||
|
GM16717 Resource Report Resource Website |
RRID:CVCL_2U49 | Homo sapiens (Human) | Transformed cell line | Male | CLO:CLO_0018457, Coriell:GM16717, Wikidata:Q54848710 |
CVCL_2U49 | 2026-09-05 10:58:04 | 0 | ||||||||
|
GM16585 Resource Report Resource Website |
Coriell Cat# GM16585, RRID:CVCL_0H39 | Cricetulus griseus (Chinese hamster) | Group: Human/rodent somatic cell hybrid. | Hybrid cell line | JH407 | Coriell | GM16585 | CLO:CLO_0017545, Coriell:GM16585, Wikidata:Q54848645 |
CVCL_0H39 | 2026-09-05 10:58:03 | 0 | |||||
|
GM16584 Resource Report Resource Website |
Coriell Cat# GM16584, RRID:CVCL_0G74 | Homo sapiens (Human) | Holoprosencephaly | PMID:23665875 | Transformed cell line | Female | JL257 | Coriell | GM16584 | CLO:CLO_0017548, Coriell:GM16584, Wikidata:Q54848644 |
CVCL_0G74 | 2026-09-05 10:58:03 | 0 | |||
|
GM16654 Resource Report Resource Website |
Coriell Cat# GM16654, RRID:CVCL_AB36 | Homo sapiens (Human) | Population: Chinese., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. |
PMID:20889555 PMID:29959025 |
Transformed cell line | Male | Coriell | GM16654 | CLO:CLO_0017363, Coriell:GM16654, Wikidata:Q54848688 |
CVCL_AB36 | 2026-09-05 10:58:04 | 0 | ||||
|
GM16635 Resource Report Resource Website |
Coriell Cat# GM16635, RRID:CVCL_F634 | Homo sapiens (Human) | Fanconi anemia, complementation group G | PMID:8782494 | Transformed cell line | Female | PD352.T | Coriell | GM16635 | CLO:CLO_0017355, Coriell:GM16635, Wikidata:Q54848678 |
cvcl_ak48 | CVCL_F634 | 2026-09-05 10:58:04 | 0 | ||
|
GM16631 Resource Report Resource Website |
Coriell Cat# GM16631, RRID:CVCL_AK40 | Homo sapiens (Human) | Fanconi anemia, complementation group A | PMID:12361951 | Finite cell line | Female | PD720.F, PD720.f, PD.720.F | Coriell | GM16631 | CLO:CLO_0017351, Coriell:GM16631, Wikidata:Q54848674 |
CVCL_AK40 | 2026-09-05 10:58:03 | 0 | |||
|
GM16530 Resource Report Resource Website |
RRID:CVCL_IW03 | Homo sapiens (Human) | Leigh disease | Characteristics: Cytoplasmic transfer (cybrid) produced by the fusion of Leigh syndrome enucleated cells GM13740 (Cellosaurus=CVCL_8A62) with cell line devoid of mitochondrial DNA (rho0) derived from 143B (Cellosaurus=CVCL_2270). | PMID:8078883 | Hybrid cell line | CLO:CLO_0017581, Coriell:GM16530, Wikidata:Q54848626 |
CVCL_IW03 | 2026-09-05 10:58:03 | 0 | ||||||
|
GM16718 Resource Report Resource Website |
Coriell Cat# GM16718, RRID:CVCL_5Q76 | Homo sapiens (Human) | Azoospermia | Population: Southeast Asian; Vietnamese. | PMID:23665875 | Transformed cell line | Male | Coriell | GM16718 | CLO:CLO_0018424, Coriell:GM16718, Wikidata:Q54848711 |
CVCL_5Q76 | 2026-09-05 10:58:04 | 0 | |||
|
GM16650 Resource Report Resource Website |
Coriell Cat# GM16650, RRID:CVCL_HJ91 | Homo sapiens (Human) | Population: Latino or Hispanic. | Finite cell line | Male | Coriell | GM16650 | Coriell:GM16650, Wikidata:Q54848685 |
CVCL_HJ91 | 2026-09-05 10:58:04 | 0 | |||||
|
GM16580 Resource Report Resource Website |
Coriell Cat# GM16580, RRID:CVCL_5Q68 | Homo sapiens (Human) | Deletion 18p syndrome | PMID:23665875 | Transformed cell line | Male | JL462 | Coriell | GM16580 | Coriell:GM16580, Wikidata:Q54848641 |
CVCL_5Q68 | 2026-09-05 10:58:03 | 0 | |||
|
GM16582 Resource Report Resource Website |
RRID:CVCL_0G73 | Homo sapiens (Human) | Holoprosencephaly | PMID:23665875 | Transformed cell line | Male | JL376 | CLO:CLO_0017552, Coriell:GM16582, Wikidata:Q54848642 |
CVCL_0G73 | 2026-09-05 10:58:03 | 0 | |||||
|
GM16563 Resource Report Resource Website |
Coriell Cat# GM16563, RRID:CVCL_H528 | Homo sapiens (Human) | Rett syndrome | Finite cell line | Female | Coriell | GM16563 | CLO:CLO_0017554, Coriell:GM16563, Wikidata:Q54848640 |
CVCL_H528 | 2026-09-05 10:58:03 | 0 | |||||
|
GM16792 Resource Report Resource Website |
RRID:CVCL_5Q78 | Homo sapiens (Human) | Deafness | PMID:23661601 | Finite cell line | Male | DD129BE | Coriell:GM16792, Wikidata:Q54848745 |
CVCL_5Q78 | 2026-09-05 10:58:05 | 0 | |||||
|
GM16790 Resource Report Resource Website |
Coriell Cat# GM16790, RRID:CVCL_CZ72 | Homo sapiens (Human) | Transformed cell line | Male | Coriell | GM16790 | CLO:CLO_0018394, Coriell:GM16790, Wikidata:Q54848743 |
CVCL_CZ72 | 2026-09-05 10:58:05 | 0 | ||||||
|
GM16967 Resource Report Resource Website |
RRID:CVCL_4D33 | Homo sapiens (Human) | Population: Caucasian; Amish. | Transformed cell line | Female | CLO:CLO_0018087, Coriell:GM16967, Wikidata:Q54848822 |
CVCL_4D33 | 2026-09-05 10:58:06 | 0 | |||||||
|
GM16800 Resource Report Resource Website |
RRID:CVCL_1F68 | Homo sapiens (Human) | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0018395, Coriell:GM16800, Wikidata:Q54848750 |
CVCL_1F68 | 2026-09-05 10:58:05 | 0 |
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