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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
DCH007 Resource Report Resource Website |
ECACC Cat# 94082283, RRID:CVCL_E551 | Homo sapiens (Human) | Population: Southeast Asian; Thai., Part of: 4th Asia-Oceania Histocompatibility Workshop (4AOHW) cell line panel. |
PMID:8307784 PMID:30844424 |
Transformed cell line | Male | DCH 007, DCH-007, Thai-DCH007 | ECACC | 94082283 | dbMHC:48747, ECACC:94082283, IHW:IHW09183, IPD-IMGT/HLA:11725, Wikidata:Q54828659 |
CVCL_E551 | 2026-07-25 04:29:21 | 0 | |||
|
DD0106 Resource Report Resource Website |
ECACC Cat# 88052403, RRID:CVCL_8U72 | Homo sapiens (Human) | Karyotypic information: 46,XY,19q+mat (ECACC=88052403)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 88052403 | ECACC:88052403, Wikidata:Q54828759 |
CVCL_8U72 | 2026-07-25 04:29:24 | 0 | |||||
|
DD0145 Resource Report Resource Website |
ECACC Cat# 91011609, RRID:CVCL_8U88 | Homo sapiens (Human) | Angelman syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91011609 | ECACC:91011609, Wikidata:Q54828777 |
CVCL_8U88 | 2026-07-25 04:29:24 | 0 | ||||
|
DD0141 Resource Report Resource Website |
ECACC Cat# 91011506, RRID:CVCL_8U84 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91011506 | ECACC:91011506, Wikidata:Q54828772 |
CVCL_8U84 | 2026-07-25 04:29:25 | 0 | |||||
|
DD0072 Resource Report Resource Website |
ECACC Cat# 90060402, RRID:CVCL_8U58 | Homo sapiens (Human) | Karyotypic information: 46,XX; 47,XX,+18 (ECACC=90060402)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 90060402 | ECACC:90060402, Wikidata:Q54828743 |
CVCL_8U58 | 2026-07-25 04:29:23 | 0 | |||||
|
DD0058 Resource Report Resource Website |
ECACC Cat# 90090604, RRID:CVCL_8U55 | Homo sapiens (Human) | Fragile X syndrome | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 90090604 | ECACC:90090604, Wikidata:Q54828740 |
CVCL_8U55 | 2026-07-25 04:29:23 | 0 | ||||
|
DD0051 Resource Report Resource Website |
ECACC Cat# 90110201, RRID:CVCL_8U51 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 90110201 | ECACC:90110201, Wikidata:Q54828732 |
CVCL_8U51 | 2026-07-25 04:29:24 | 0 | |||||
|
DD0073 Resource Report Resource Website |
ECACC Cat# 90042503, RRID:CVCL_8U59 | Homo sapiens (Human) | Karyotypic information: 46,XX; 47,XX,+mar mat (ECACC=90042503)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 90042503 | ECACC:90042503, Wikidata:Q54828744 |
CVCL_8U59 | 2026-07-25 04:29:23 | 0 | |||||
|
DD0098 Resource Report Resource Website |
ECACC Cat# 89070501, RRID:CVCL_8U66 | Homo sapiens (Human) | Fragile X syndrome | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 89070501 | ECACC:89070501, Wikidata:Q54828751 |
CVCL_8U66 | 2026-07-25 04:29:24 | 0 | ||||
|
DD0108 Resource Report Resource Website |
ECACC Cat# 870424011, RRID:CVCL_8U73 | Homo sapiens (Human) | Karyotypic information: 47,XX,+dic(15)(pter->q11::q11->pter) (ECACC=870424011)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 870424011 | ECACC:870424011, Wikidata:Q54828760 |
CVCL_8U73 | 2026-07-25 04:29:23 | 0 | |||||
|
DD0102 Resource Report Resource Website |
ECACC Cat# 89021601, RRID:CVCL_8U69 | Homo sapiens (Human) | Fragile X syndrome | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 89021601 | ECACC:89021601, Wikidata:Q54828755 |
CVCL_8U69 | 2026-07-25 04:29:24 | 0 | ||||
|
DD0100 Resource Report Resource Website |
ECACC Cat# 89031702, RRID:CVCL_8U68 | Homo sapiens (Human) | Methylmalonic acidemia | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 89031702 | ECACC:89031702, Wikidata:Q54828754 |
CVCL_8U68 | 2026-07-25 04:29:23 | 0 | ||||
|
DD0034 Resource Report Resource Website |
ECACC Cat# 90092605, RRID:CVCL_8U43 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 90092605 | ECACC:90092605, Wikidata:Q54828721 |
CVCL_8U43 | 2026-07-25 04:29:22 | 0 | |||||
|
DD0140 Resource Report Resource Website |
ECACC Cat# 91011103, RRID:CVCL_8U83 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91011103 | ECACC:91011103, Wikidata:Q54828771 |
CVCL_8U83 | 2026-07-25 04:29:23 | 0 | |||||
|
DD0086 Resource Report Resource Website |
ECACC Cat# 90010302, RRID:CVCL_8U63 | Homo sapiens (Human) | Karyotypic information: 46,XX; 46,XX,t(2;11) (ECACC=90010302)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 90010302 | ECACC:90010302, Wikidata:Q54828748 |
CVCL_8U63 | 2026-07-25 04:29:24 | 0 | |||||
|
DD0054 Resource Report Resource Website |
ECACC Cat# 90112722, RRID:CVCL_8U52 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 90112722 | ECACC:90112722, Wikidata:Q54828733 |
CVCL_8U52 | 2026-07-25 04:29:23 | 0 | |||||
|
DD0041 Resource Report Resource Website |
ECACC Cat# 90100701, RRID:CVCL_8U47 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 90100701 | ECACC:90100701, Wikidata:Q54828726 |
CVCL_8U47 | 2026-07-25 04:29:22 | 0 | |||||
|
DD0056 Resource Report Resource Website |
ECACC Cat# 90091701, RRID:CVCL_8U53 | Homo sapiens (Human) | Karyotypic information: 46,XY,t(4;9)(p16;q32)pat (ECACC=90091701)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 90091701 | ECACC:90091701, Wikidata:Q54828734 |
CVCL_8U53 | 2026-07-25 04:29:23 | 0 | |||||
|
DD0133 Resource Report Resource Website |
ECACC Cat# 91010902, RRID:CVCL_8U81 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91010902 | ECACC:91010902, Wikidata:Q54828769 |
CVCL_8U81 | 2026-07-25 04:29:25 | 0 | |||||
|
DD0105 Resource Report Resource Website |
ECACC Cat# 88101401, RRID:CVCL_8U71 | Homo sapiens (Human) | Methylmalonic acidemia | Karyotypic information: 46,XY,fra(X)(q28) 16/50 (ECACC=88101401)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 88101401 | ECACC:88101401, Wikidata:Q54828758 |
CVCL_8U71 | 2026-07-25 04:29:23 | 0 |
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