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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
DD0199 Resource Report Resource Website |
ECACC Cat# 91030612, RRID:CVCL_8V18 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91030612 | ECACC:91030612, Wikidata:Q54828819 |
CVCL_8V18 | 2026-07-25 04:29:25 | 0 | |||||
|
DD0155 Resource Report Resource Website |
ECACC Cat# 91012608, RRID:CVCL_8U95 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91012608 | ECACC:91012608, Wikidata:Q54828794 |
CVCL_8U95 | 2026-07-25 04:29:24 | 0 | |||||
|
DD0226 Resource Report Resource Website |
ECACC Cat# 91032716, RRID:CVCL_8V34 | Homo sapiens (Human) | Fragile X syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91032716 | ECACC:91032716, Wikidata:Q54828844 |
CVCL_8V34 | 2026-07-25 04:29:27 | 0 | ||||
|
DD0204 Resource Report Resource Website |
ECACC Cat# 91031307, RRID:CVCL_8V22 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91031307 | ECACC:91031307, Wikidata:Q54828823 |
CVCL_8V22 | 2026-07-25 04:29:26 | 0 | |||||
|
DD0222 Resource Report Resource Website |
ECACC Cat# 91032619, RRID:CVCL_8V31 | Homo sapiens (Human) | Karyotypic information: 46,XY,t(6;22)(p21.3;q13)pat (ECACC=91032619)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91032619 | ECACC:91032619, Wikidata:Q54828832 |
CVCL_8V31 | 2026-07-25 04:29:26 | 0 | |||||
|
DD0225 Resource Report Resource Website |
ECACC Cat# 91032715, RRID:CVCL_8V33 | Homo sapiens (Human) | Angelman syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91032715 | ECACC:91032715, Wikidata:Q54828834 |
CVCL_8V33 | 2026-07-25 04:29:25 | 0 | ||||
|
DD0185 Resource Report Resource Website |
ECACC Cat# 91022219, RRID:CVCL_8V07 | Homo sapiens (Human) | Karyotypic information: 46,XY,t(11;22)(q23;q11) (ECACC=91022219)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91022219 | ECACC:91022219, Wikidata:Q54828807 |
CVCL_8V07 | 2026-07-25 04:29:26 | 0 | |||||
|
DD0206 Resource Report Resource Website |
ECACC Cat# 91031816, RRID:CVCL_8V23 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(2;12)(q37;q24.1) (ECACC=91031816)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91031816 | ECACC:91031816, Wikidata:Q54828824 |
CVCL_8V23 | 2026-07-25 04:29:25 | 0 | |||||
|
DD0182 Resource Report Resource Website |
ECACC Cat# 91022216, RRID:CVCL_8V04 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(5;18)(p13;q11)pat (ECACC=91022216)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91022216 | ECACC:91022216, Wikidata:Q54828804 |
CVCL_8V04 | 2026-07-25 04:29:26 | 0 | |||||
|
DD0203 Resource Report Resource Website |
ECACC Cat# 91030815, RRID:CVCL_8V21 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(10;20)(q23;q13.3) (ECACC=91030815)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91030815 | ECACC:91030815, Wikidata:Q54828822 |
CVCL_8V21 | 2026-07-25 04:29:25 | 0 | |||||
|
DD0218 Resource Report Resource Website |
ECACC Cat# 91032114, RRID:CVCL_8V29 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91032114 | ECACC:91032114, Wikidata:Q54828830 |
CVCL_8V29 | 2026-07-25 04:29:25 | 0 | |||||
|
DD0178 Resource Report Resource Website |
ECACC Cat# 91021432, RRID:CVCL_8V02 | Homo sapiens (Human) | Karyotypic information: 46,X,der(X),t(X;5)(p22.33;p15.1)mat (ECACC=91021432)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91021432 | ECACC:91021432, Wikidata:Q54828802 |
CVCL_8V02 | 2026-07-25 04:29:24 | 0 | |||||
|
DD0193 Resource Report Resource Website |
ECACC Cat# 91030407, RRID:CVCL_8V13 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91030407 | ECACC:91030407, Wikidata:Q54828813 |
CVCL_8V13 | 2026-07-25 04:29:26 | 0 | |||||
|
DD0150 Resource Report Resource Website |
ECACC Cat# 91012213, RRID:CVCL_8U91 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91012213 | ECACC:91012213, Wikidata:Q54828780 |
CVCL_8U91 | 2026-07-25 04:29:24 | 0 | |||||
|
DD0187 Resource Report Resource Website |
ECACC Cat# 91022705, RRID:CVCL_8V09 | Homo sapiens (Human) | Fragile X syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91022705 | ECACC:91022705, Wikidata:Q54828809 |
CVCL_8V09 | 2026-07-25 04:29:24 | 0 | ||||
|
DD0152 Resource Report Resource Website |
ECACC Cat# 91012605, RRID:CVCL_8U92 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91012605 | ECACC:91012605, Wikidata:Q54828781 |
CVCL_8U92 | 2026-07-25 04:29:24 | 0 | |||||
|
DD0260 Resource Report Resource Website |
ECACC Cat# 91043007, RRID:CVCL_8V60 | Homo sapiens (Human) | Karyotypic information: 46,X,t(X;4)(p22;q27); de novo,var(13p+)mat (ECACC=91043007)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91043007 | ECACC:91043007, Wikidata:Q54828875 |
CVCL_8V60 | 2026-07-25 04:29:26 | 0 | |||||
|
DD0277 Resource Report Resource Website |
ECACC Cat# 91051503, RRID:CVCL_8V74 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91051503 | ECACC:91051503, Wikidata:Q54828894 |
CVCL_8V74 | 2026-07-25 04:29:26 | 0 | |||||
|
DD0264 Resource Report Resource Website |
ECACC Cat# 91050204, RRID:CVCL_8V64 | Homo sapiens (Human) | Trisomy 18 | Karyotypic information: 47,XX,+18 (ECACC=91050204)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 91050204 | ECACC:91050204, Wikidata:Q54828879 |
CVCL_8V64 | 2026-07-25 04:29:28 | 0 | ||||
|
DD0272 Resource Report Resource Website |
ECACC Cat# 91050812, RRID:CVCL_8V70 | Homo sapiens (Human) | Trisomy 18 | Karyotypic information: 47,XX,+18 (ECACC=91050812)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 91050812 | ECACC:91050812, Wikidata:Q54828885 |
CVCL_8V70 | 2026-07-25 04:29:28 | 0 |
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