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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM16555 Resource Report Resource Website |
Coriell Cat# GM16555, RRID:CVCL_JX69 | Homo sapiens (Human) | Prune belly syndrome | Finite cell line | Male | Coriell | GM16555 | CLO:CLO_0017556, Coriell:GM16555, Wikidata:Q54848638 |
CVCL_JX69 | 2026-09-05 10:58:03 | 0 | |||||
|
GM16633 Resource Report Resource Website |
RRID:CVCL_G042 | Homo sapiens (Human) | Fanconi anemia, complementation group D2 |
PMID:7581463 PMID:12361951 |
Transformed cell line | Male | PD20 hygro, PD.20hygro, PD-20, PD20 | CLO:CLO_0017357, EFO:EFO_0022708, Coriell:GM16633, Wikidata:Q54848676 |
CVCL_G042 | 2026-09-05 10:58:03 | 0 | |||||
|
GM16586 Resource Report Resource Website |
Coriell Cat# GM16586, RRID:CVCL_0G75 | Homo sapiens (Human) | Holoprosencephaly |
PMID:7485158 PMID:23665875 |
Transformed cell line | Male | JL218 | Coriell | GM16586 | CLO:CLO_0017390, Coriell:GM16586, Wikidata:Q54848646 |
CVCL_0G75 | 2026-09-05 10:58:03 | 0 | |||
|
GM16594 Resource Report Resource Website |
RRID:CVCL_5Q72 | Cricetulus griseus (Chinese hamster) | Group: Human/rodent somatic cell hybrid. | Hybrid cell line | JH517 | CLO:CLO_0017400, Coriell:GM16594, Wikidata:Q54848669 |
CVCL_5Q72 | 2026-09-05 10:58:03 | 0 | |||||||
|
GM16652 Resource Report Resource Website |
Coriell Cat# GM16652, RRID:CVCL_HJ93 | Homo sapiens (Human) | Trichothiodystrophy | Population: Latino or Hispanic. | Finite cell line | Male | Coriell | GM16652 | Coriell:GM16652, Wikidata:Q54848687 |
CVCL_HJ93 | 2026-09-05 10:58:04 | 0 | ||||
|
GM16718 Resource Report Resource Website |
RRID:CVCL_5Q76 | Homo sapiens (Human) | Azoospermia | Population: Southeast Asian; Vietnamese. | PMID:23665875 | Transformed cell line | Male | CLO:CLO_0018424, Coriell:GM16718, Wikidata:Q54848711 |
CVCL_5Q76 | 2026-09-05 10:58:04 | 0 | |||||
|
GM16548 Resource Report Resource Website |
RRID:CVCL_4F42 | Homo sapiens (Human) | Rett syndrome | PMID:21074045 | Finite cell line | Female | CLO:CLO_0017557, Coriell:GM16548, Wikidata:Q54848634 |
CVCL_4F42 | 2026-09-05 10:58:03 | 0 | ||||||
|
GM16647 Resource Report Resource Website |
Coriell Cat# GM16647, RRID:CVCL_HJ88 | Homo sapiens (Human) | Population: Latino or Hispanic. | Transformed cell line | Female | Coriell | GM16647 | Coriell:GM16647, Wikidata:Q54848682 |
CVCL_HJ88 | 2026-09-05 10:58:04 | 0 | |||||
|
GM16654 Resource Report Resource Website |
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 | CLO:CLO_0017363, Coriell:GM16654, Wikidata:Q54848688 |
CVCL_AB36 | 2026-09-05 10:58:04 | 0 | ||||||
|
GM16733 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM16733, RRID:CVCL_YP91 | Homo sapiens (Human) | Population: Caucasian. | PMID:23661601 | Finite cell line | Female | Coriell | GM16733 | Coriell:GM16733, Wikidata:Q93847995 |
CVCL_YP91 | 2026-09-05 10:58:04 | 0 | ||||
|
GM16530 Resource Report Resource Website |
Coriell Cat# GM16530, 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 | Coriell | GM16530 | CLO:CLO_0017581, Coriell:GM16530, Wikidata:Q54848626 |
CVCL_IW03 | 2026-09-05 10:58:03 | 0 | ||||
|
GM16580 Resource Report Resource Website |
RRID:CVCL_5Q68 | Homo sapiens (Human) | Deletion 18p syndrome | PMID:23665875 | Transformed cell line | Male | JL462 | Coriell:GM16580, Wikidata:Q54848641 |
CVCL_5Q68 | 2026-09-05 10:58:03 | 0 | |||||
|
GM16649 Resource Report Resource Website |
Coriell Cat# GM16649, RRID:CVCL_HJ90 | Homo sapiens (Human) | Population: Latino or Hispanic. | Transformed cell line | Male | Coriell | GM16649 | Coriell:GM16649, Wikidata:Q54848684 |
CVCL_HJ90 | 2026-09-05 10:58:04 | 0 | |||||
|
GM16549 Resource Report Resource Website |
Coriell Cat# GM16549, RRID:CVCL_X436 | Homo sapiens (Human) | Smith-Lemli-Opitz syndrome | Finite cell line | Male | Coriell | GM16549 | Coriell:GM16549, Wikidata:Q54848637 |
CVCL_X436 | 2026-09-05 10:58:03 | 0 | |||||
|
GM16598 Resource Report Resource Website |
Coriell Cat# GM16598, RRID:CVCL_5Q74 | Homo sapiens (Human) | Cri du chat syndrome | PMID:23665875 | Transformed cell line | Male | JL88 | Coriell | GM16598 | CLO:CLO_0017405, Coriell:GM16598, Wikidata:Q54848671 |
CVCL_5Q74 | 2026-09-05 10:58:03 | 0 | |||
|
GM16587 Resource Report Resource Website |
Coriell Cat# GM16587, RRID:CVCL_0G76 | Cricetulus griseus (Chinese hamster) | Group: Human/rodent somatic cell hybrid. | PMID:7485158 | Hybrid cell line | JH360 | Coriell | GM16587 | CLO:CLO_0017393, Coriell:GM16587, Wikidata:Q54848648 |
CVCL_0G76 | 2026-09-05 10:58:03 | 0 | ||||
|
GM16645 Resource Report Resource Website |
RRID:CVCL_HJ86 | Homo sapiens (Human) | Population: Latino or Hispanic. | Transformed cell line | Female | Coriell:GM16645, Wikidata:Q54848680 |
CVCL_HJ86 | 2026-09-05 10:58:04 | 0 | |||||||
|
GM16535 Resource Report Resource Website |
RRID:CVCL_DB92 | Homo sapiens (Human) | Hereditary melanoma with CDKN2A mutation | Donor information: At sampling donor was not affected with cutaneous malignant melanoma 2 but at risk for disease (mutation in CDKN2A start site). | Transformed cell line | Female | CLO:CLO_0017579, Coriell:GM16535, Wikidata:Q54848630 |
CVCL_DB92 | 2026-09-05 10:58:03 | 0 | ||||||
|
GM16734 Resource Report Resource Website |
Coriell Cat# GM18097, RRID:CVCL_N267 | Homo sapiens (Human) | Population: Caucasian., Part of: Human variation panel. | PMID:23661601 | Transformed cell line | Male | GM16734A, GM18097 | Coriell | GM18097 | CLO:CLO_0015749, CLO:CLO_0018429, Coriell:GM16734, Coriell:GM18097, Wikidata:Q54848719 |
CVCL_N267 | 2026-09-05 10:58:04 | 0 | |||
|
GM16593 Resource Report Resource Website |
RRID:CVCL_5Q71 | Homo sapiens (Human) | Cri du chat syndrome | PMID:23665875 | Transformed cell line | Female | JL444 | CLO:CLO_0017398, Coriell:GM16593, Wikidata:Q54848668 |
CVCL_5Q71 | 2026-09-05 10:58:03 | 0 |
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The data sets included in this resource are published in Kravitz et al, 2012. Distinct roles for direct and indirect pathway striatal neurons in reinforcement (Nat. Neurosci).
