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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
AG08508 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A2DW | Homo sapiens (Human) | Population: Caucasian; German., Part of: German Alzheimer disease kindred subcollection. | Transformed cell line | Male | AG08508B | Coriell:AG08508, Wikidata:Q105506306 |
CVCL_A2DW | 2026-09-05 11:45:10 | 0 | ||||||
|
AG0862 Resource Report Resource Website Discontinued |
ECACC Cat# 94080540, RRID:CVCL_8B73 | Homo sapiens (Human) | Coffin-Lowry syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 94080540 | ECACC:94080540, Wikidata:Q54742343 |
CVCL_8B73 | 2026-09-05 11:45:13 | 0 | ||||
|
AG0861 Resource Report Resource Website Discontinued |
ECACC Cat# 94080539, RRID:CVCL_8B72 | Homo sapiens (Human) | Coffin-Lowry syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 94080539 | ECACC:94080539, Wikidata:Q54742330 |
CVCL_8B72 | 2026-09-05 11:45:13 | 0 | ||||
|
AG0881 Resource Report Resource Website Discontinued |
RRID:CVCL_8B75 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:94101408, Wikidata:Q54742542 |
CVCL_8B75 | 2026-09-05 11:45:14 | 0 | |||||||
|
AG0882 Resource Report Resource Website Discontinued |
ECACC Cat# 94101409, RRID:CVCL_8B76 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 94101409 | ECACC:94101409, Wikidata:Q54742550 |
CVCL_8B76 | 2026-09-05 11:45:14 | 0 | |||||
|
AG0883 Resource Report Resource Website Discontinued |
RRID:CVCL_8B77 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC:94101410, Wikidata:Q54742552 |
CVCL_8B77 | 2026-09-05 11:45:14 | 0 | |||||||
|
AG09128 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_2Q58 | Homo sapiens (Human) | Alzheimer's disease 3 | Donor information: At sampling donor was not affected with Alzheimer disease but has a 50% risk., Population: Caucasian; Italian. | Transformed cell line | Female | CLO:CLO_0021850, Coriell:AG09128, Wikidata:Q54742712 |
CVCL_2Q58 | 2026-09-05 11:45:16 | 0 | ||||||
|
AG09128 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG09128, RRID:CVCL_2Q58 | Homo sapiens (Human) | Alzheimer's disease 3 | Donor information: At sampling donor was not affected with Alzheimer disease but has a 50% risk., Population: Caucasian; Italian. | Transformed cell line | Female | Coriell | AG09128 | CLO:CLO_0021850, Coriell:AG09128, Wikidata:Q54742712 |
CVCL_2Q58 | 2026-09-05 11:45:16 | 0 | ||||
|
AG0920 Resource Report Resource Website Discontinued |
ECACC Cat# 95030321, RRID:CVCL_8B78 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 95030321 | ECACC:95030321, Wikidata:Q54742825 |
CVCL_8B78 | 2026-09-05 11:45:17 | 0 | |||||
|
AG09179 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG09179, RRID:CVCL_4L72 | Homo sapiens (Human) | Population: Caucasian; German., Part of: German Alzheimer disease kindred subcollection. | Finite cell line | Male | Coriell | AG09179 | Coriell:AG09179, Wikidata:Q54742803 |
CVCL_4L72 | 2026-09-05 11:45:17 | 0 | |||||
|
AG03307 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG03307, RRID:CVCL_A2KV | Homo sapiens (Human) | Junctional nevus | PMID:7253718 | Finite cell line | Female | AG3307 | Coriell | AG03307 | Coriell:AG03307, Wikidata:Q105506165 |
CVCL_A2KV | 2026-09-05 11:44:45 | 0 | |||
|
AG02653 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG02653, RRID:CVCL_A2LU | Homo sapiens (Human) | PMID:7253718 | Finite cell line | Female | AG2653 | Coriell | AG02653 | Coriell:AG02653, Wikidata:Q105506142 |
CVCL_A2LU | 2026-09-05 11:44:44 | 0 | ||||
|
AG03302 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG03302, RRID:CVCL_A2KU | Homo sapiens (Human) | PMID:7253718 | Finite cell line | Male | AG3302 | Coriell | AG03302 | Coriell:AG03302, Wikidata:Q105506162 |
CVCL_A2KU | 2026-09-05 11:44:45 | 0 | ||||
|
AG03309 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# AG03309, RRID:CVCL_A2KX | Homo sapiens (Human) | PMID:7253718 | Finite cell line | Female | AG3309 | Coriell | AG03309 | Coriell:AG03309, Wikidata:Q105506173 |
CVCL_A2KX | 2026-09-05 11:44:45 | 0 | ||||
|
AG03354 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A2EF | Homo sapiens (Human) | Cystic fibrosis | PMID:7253718 | Finite cell line | Sex unspecified | AG3354 | Coriell:AG03354, Wikidata:Q105506182 |
CVCL_A2EF | 2026-09-05 11:44:46 | 0 | |||||
|
AG03848 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A2MM | Homo sapiens (Human) | Werdnig-Hoffmann disease |
PMID:3941662 PMID:7253718 |
Finite cell line | Male | AG 3848, AG3848, SMA2FABE | Coriell:AG03848, Wikidata:Q105506266 |
CVCL_A2MM | 2026-09-05 11:44:47 | 0 | |||||
|
AG03607 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A2ME | Homo sapiens (Human) | PMID:7253718 | Finite cell line | Female | AG3607 | Coriell:AG03607, Wikidata:Q105506215 |
CVCL_A2ME | 2026-09-05 11:44:46 | 0 | ||||||
|
AG03730 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A2MI | Homo sapiens (Human) | Spinal muscular atrophy | PMID:7253718 | Finite cell line | Male | AG3730 | Coriell:AG03730, Wikidata:Q105506245 |
CVCL_A2MI | 2026-09-05 11:44:47 | 0 | |||||
|
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 | 2026-09-05 11:44:47 | 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 | 2026-09-05 11:44:47 | 0 |
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