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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
AG03819 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG03819, RRID:CVCL_A2ML | Homo sapiens (Human) | Spinocerebellar ataxia | PMID:7253718 | Finite cell line | Female | AG3819 | Coriell | AG03819 | Coriell:AG03819, Wikidata:Q105506261 |
CVCL_A2ML | 2026-08-01 05:57:43 | 0 | |||
|
AG03739 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_2A31 | Homo sapiens (Human) | Dyskeratosis congenita | Population: Caucasian. | Transformed cell line | Male | AG03739A | CLO:CLO_0036957, Coriell:AG03739, Wikidata:Q54609784 |
CVCL_2A31 | 2026-08-01 05:57:43 | 0 | |||||
|
AG03927 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A2MP | Homo sapiens (Human) | PMID:7253718 | Transformed cell line | Female | AG3927 | Coriell:AG03927, Wikidata:Q105506275 |
CVCL_A2MP | 2026-08-01 05:57:43 | 0 | ||||||
|
AG03692 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A2KM | Homo sapiens (Human) | PMID:7253718 | Finite cell line | Male | AG3692 | Coriell:AG03692, Wikidata:Q105506241 |
CVCL_A2KM | 2026-08-01 05:57:43 | 0 | ||||||
|
AG03635 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A2KQ | Homo sapiens (Human) | PMID:7253718 | Transformed cell line | Sex unspecified | AG3635 | Coriell:AG03635, Wikidata:Q105506223 |
CVCL_A2KQ | 2026-08-01 05:57:43 | 0 | ||||||
|
AG03594 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A2MD | Homo sapiens (Human) | Werner syndrome | PMID:7253718 | Finite cell line | Male | AG3594 | Coriell:AG03594, Wikidata:Q105506213 |
CVCL_A2MD | 2026-08-01 05:57:41 | 0 | |||||
|
AG03758 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG03758, RRID:CVCL_A2EC | Homo sapiens (Human) | Charcot-Marie-Tooth disease | PMID:7253718 | Finite cell line | Female | AG3758 | Coriell | AG03758 | Coriell:AG03758, Wikidata:Q105506249 |
CVCL_A2EC | 2026-08-01 05:57:43 | 0 | |||
|
AG03674 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG03674, RRID:CVCL_A2MF | Homo sapiens (Human) | Progressive supranuclear palsy | PMID:7253718 | Transformed cell line | Male | AG3674 | Coriell | AG03674 | Coriell:AG03674, Wikidata:Q105506229 |
CVCL_A2MF | 2026-08-01 05:57:41 | 0 | |||
|
AG03927 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG03927, RRID:CVCL_A2MP | Homo sapiens (Human) | PMID:7253718 | Transformed cell line | Female | AG3927 | Coriell | AG03927 | Coriell:AG03927, Wikidata:Q105506275 |
CVCL_A2MP | 2026-08-01 05:57:42 | 0 | ||||
|
AG03758 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A2EC | Homo sapiens (Human) | Charcot-Marie-Tooth disease | PMID:7253718 | Finite cell line | Female | AG3758 | Coriell:AG03758, Wikidata:Q105506249 |
CVCL_A2EC | 2026-08-01 05:57:41 | 0 | |||||
|
AG03634 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A2KP | Homo sapiens (Human) | PMID:7253718 | Finite cell line | Sex unspecified | AG3634 | Coriell:AG03634, Wikidata:Q105506220 |
CVCL_A2KP | 2026-08-01 05:57:41 | 0 | ||||||
|
AG03678 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A2MG | Homo sapiens (Human) | Progressive supranuclear palsy | PMID:7253718 | Finite cell line | Male | AG3678 | Coriell:AG03678, Wikidata:Q105506235 |
CVCL_A2MG | 2026-08-01 05:57:41 | 0 | |||||
|
AG03690 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG03690, RRID:CVCL_A2MH | Homo sapiens (Human) | Kidney Wilms tumor | PMID:7253718 | Finite cell line | Female | AG3690 | Coriell | AG03690 | Coriell:AG03690, Wikidata:Q105506237 |
CVCL_A2MH | 2026-08-01 05:57:41 | 0 | |||
|
AG03849 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG03849, RRID:CVCL_A2MN | Homo sapiens (Human) |
PMID:3941662 PMID:7253718 |
Finite cell line | Female | AG 3849, AG3849, SMAM2FABE | Coriell | AG03849 | Coriell:AG03849, Wikidata:Q105506270 |
CVCL_A2MN | 2026-08-01 05:57:41 | 0 | ||||
|
AG03805 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A2MJ | Homo sapiens (Human) | Spinal muscular atrophy | PMID:7253718 | Finite cell line | Male | AG3805 | Coriell:AG03805, Wikidata:Q105506251 |
CVCL_A2MJ | 2026-08-01 05:57:41 | 0 | |||||
|
AG03607 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG03607, RRID:CVCL_A2ME | Homo sapiens (Human) | PMID:7253718 | Finite cell line | Female | AG3607 | Coriell | AG03607 | Coriell:AG03607, Wikidata:Q105506215 |
CVCL_A2ME | 2026-08-01 05:57:41 | 0 | ||||
|
AG03633 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG03633, RRID:CVCL_A2KN | Homo sapiens (Human) | PMID:7253718 | Transformed cell line | AG3633 | Coriell | AG03633 | Coriell:AG03633, Wikidata:Q105506217 |
CVCL_A2KN | 2026-08-01 05:57:43 | 0 | |||||
|
AG0425 Resource Report Resource Website Discontinued |
RRID:CVCL_8B59 | Homo sapiens (Human) | 22q11.2 deletion syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:91082128, Wikidata:Q54609958 |
CVCL_8B59 | 2026-08-01 05:57:45 | 0 | ||||||
|
AG0441 Resource Report Resource Website Discontinued |
RRID:CVCL_8B63 | Homo sapiens (Human) | 22q11.2 deletion syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC:91092607, Wikidata:Q54610105 |
CVCL_8B63 | 2026-08-01 05:57:44 | 0 | ||||||
|
AG0422 Resource Report Resource Website Discontinued |
RRID:CVCL_8B57 | Homo sapiens (Human) | 22q11.2 deletion syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:91081203, Wikidata:Q54609953 |
CVCL_8B57 | 2026-08-01 05:57:42 | 0 |
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