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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
DD2309 Resource Report Resource Website |
ECACC Cat# 95061206, RRID:CVCL_9J55 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 95061206 | ECACC:95061206, Wikidata:Q54830205 |
CVCL_9J55 | 2026-07-25 04:29:58 | 0 | ||||
|
DD2248 Resource Report Resource Website |
ECACC Cat# 95040614, RRID:CVCL_9J36 | Homo sapiens (Human) | Ebstein anomaly | Karyotypic information: 46,XX.ish,22q11.2(cH748x2) (ECACC=95040614)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 95040614 | ECACC:95040614, Wikidata:Q54830183 |
CVCL_9J36 | 2026-07-25 04:29:57 | 0 | ||||
|
DD2218 Resource Report Resource Website |
ECACC Cat# 95022816, RRID:CVCL_AQ90 | Homo sapiens (Human) | Roberts syndrome | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 95022816 | ECACC:95022816, Wikidata:Q54830168 |
CVCL_AQ90 | 2026-07-25 04:29:57 | 0 | ||||
|
DD2243 Resource Report Resource Website |
ECACC Cat# 95033119, RRID:CVCL_AQ93 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 95033119 | ECACC:95033119, Wikidata:Q54830182 |
CVCL_AQ93 | 2026-07-25 04:29:57 | 0 | |||||
|
DD2320 Resource Report Resource Website |
ECACC Cat# 95061610, RRID:CVCL_9J63 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 95061610 | ECACC:95061610, Wikidata:Q54830213 |
CVCL_9J63 | 2026-07-25 04:29:58 | 0 | ||||
|
DD2312 Resource Report Resource Website |
ECACC Cat# 95061310, RRID:CVCL_9J58 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 95061310 | ECACC:95061310, Wikidata:Q54830208 |
CVCL_9J58 | 2026-07-25 04:29:58 | 0 | ||||
|
DD2282 Resource Report Resource Website |
ECACC Cat# 95053003, RRID:CVCL_9J46 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 95053003 | ECACC:95053003, Wikidata:Q54830195 |
CVCL_9J46 | 2026-07-25 04:29:57 | 0 | ||||
|
DD2278 Resource Report Resource Website |
ECACC Cat# 95052403, RRID:CVCL_9J44 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 95052403 | ECACC:95052403, Wikidata:Q54830193 |
CVCL_9J44 | 2026-07-25 04:29:57 | 0 | ||||
|
DD2308 Resource Report Resource Website |
ECACC Cat# 95060915, RRID:CVCL_9J54 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 95060915 | ECACC:95060915, Wikidata:Q54830204 |
CVCL_9J54 | 2026-07-25 04:29:58 | 0 | ||||
|
DD2259 Resource Report Resource Website |
ECACC Cat# 95042830, RRID:CVCL_9J39 | Homo sapiens (Human) | Trisomy 8 | Karyotypic information: 47,XY,+8 (ECACC=95042830)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 95042830 | ECACC:95042830, Wikidata:Q54830186 |
CVCL_9J39 | 2026-07-25 04:29:57 | 0 | ||||
|
DD2295 Resource Report Resource Website |
ECACC Cat# 95060304, RRID:CVCL_9J50 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 95060304 | ECACC:95060304, Wikidata:Q54830199 |
CVCL_9J50 | 2026-07-25 04:29:57 | 0 | ||||
|
DD2285 Resource Report Resource Website |
ECACC Cat# 95053109, RRID:CVCL_9J47 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 95053109 | ECACC:95053109, Wikidata:Q54830196 |
CVCL_9J47 | 2026-07-25 04:29:57 | 0 | ||||
|
DD2274 Resource Report Resource Website |
ECACC Cat# 95051228, RRID:CVCL_9J42 | Homo sapiens (Human) | Smith-Magenis syndrome | Karyotypic information: 46,XY,del(17)(p11.2;p11.2) (ECACC=95051228)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 95051228 | ECACC:95051228, Wikidata:Q54830191 |
CVCL_9J42 | 2026-07-25 04:29:57 | 0 | ||||
|
DD2235 Resource Report Resource Website |
ECACC Cat# 95032427, RRID:CVCL_9J34 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 95032427 | ECACC:95032427, Wikidata:Q54830176 |
CVCL_9J34 | 2026-07-25 04:29:57 | 0 | |||||
|
DD2208 Resource Report Resource Website |
ECACC Cat# 95021603, RRID:CVCL_9J26 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 95021603 | ECACC:95021603, Wikidata:Q54830166 |
CVCL_9J26 | 2026-07-25 04:29:57 | 0 | |||||
|
DD2319 Resource Report Resource Website |
ECACC Cat# 95061609, RRID:CVCL_9J62 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 95061609 | ECACC:95061609, Wikidata:Q54830212 |
CVCL_9J62 | 2026-07-25 04:29:58 | 0 | ||||
|
DD2255 Resource Report Resource Website |
ECACC Cat# 95042114, RRID:CVCL_9J38 | Homo sapiens (Human) | Karyotypic information: 46,XY,inv(2)(q31.3;q37.1)mat (ECACC=95042114)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 95042114 | ECACC:95042114, Wikidata:Q54830185 |
CVCL_9J38 | 2026-07-25 04:29:57 | 0 | |||||
|
DD2222 Resource Report Resource Website |
ECACC Cat# 95030627, RRID:CVCL_9J28 | Homo sapiens (Human) | Karyotypic information: 46,XX; 46,X,r(X) (ECACC=95030627)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 95030627 | ECACC:95030627, Wikidata:Q54830170 |
CVCL_9J28 | 2026-07-25 04:29:57 | 0 | |||||
|
DD2242 Resource Report Resource Website |
ECACC Cat# 95033118, RRID:CVCL_AQ92 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 95033118 | ECACC:95033118, Wikidata:Q54830181 |
CVCL_AQ92 | 2026-07-25 04:29:57 | 0 | |||||
|
DD2206 Resource Report Resource Website |
ECACC Cat# 95021601, RRID:CVCL_9J24 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 95021601 | ECACC:95021601, Wikidata:Q54830164 |
CVCL_9J24 | 2026-07-25 04:29:56 | 0 |
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