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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
DD3310 Resource Report Resource Website |
ECACC Cat# 98111804, RRID:CVCL_9M88 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98111804 | ECACC:98111804, Wikidata:Q54830685 |
CVCL_9M88 | 2026-08-29 04:25:26 | 0 | |||||
|
DD3271 Resource Report Resource Website |
ECACC Cat# 98102905, RRID:CVCL_9P09 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 98102905 | ECACC:98102905, Wikidata:Q54830655 |
CVCL_9P09 | 2026-08-29 04:25:25 | 0 | |||||
|
DD3306 Resource Report Resource Website |
ECACC Cat# 98111707, RRID:CVCL_9M87 | Homo sapiens (Human) | Karyotypic information: 46,XX,inv(17)(p?11;q?12) (ECACC=98111707)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 98111707 | ECACC:98111707, Wikidata:Q54830683 |
CVCL_9M87 | 2026-08-29 04:25:26 | 0 | |||||
|
DD3276 Resource Report Resource Website |
ECACC Cat# 98102910, RRID:CVCL_9P14 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 98102910 | ECACC:98102910, Wikidata:Q54830660 |
CVCL_9P14 | 2026-08-29 04:25:27 | 0 | |||||
|
DD3266 Resource Report Resource Website |
ECACC Cat# 98102817, RRID:CVCL_9M78 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98102817 | ECACC:98102817, Wikidata:Q54830649 |
CVCL_9M78 | 2026-08-29 04:25:26 | 0 | ||||
|
DD3282 Resource Report Resource Website |
ECACC Cat# 98102916, RRID:CVCL_9P20 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98102916 | ECACC:98102916, Wikidata:Q54830666 |
CVCL_9P20 | 2026-08-29 04:25:27 | 0 | |||||
|
DD3279 Resource Report Resource Website |
ECACC Cat# 98102913, RRID:CVCL_9P17 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 98102913 | ECACC:98102913, Wikidata:Q54830663 |
CVCL_9P17 | 2026-08-29 04:25:27 | 0 | |||||
|
DD3291 Resource Report Resource Website |
ECACC Cat# 98103010, RRID:CVCL_9M82 | Homo sapiens (Human) | Type 1 diabetes mellitus | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98103010 | ECACC:98103010, Wikidata:Q54830675 |
CVCL_9M82 | 2026-08-29 04:25:27 | 0 | ||||
|
DD3333 Resource Report Resource Website |
ECACC Cat# 98121502, RRID:CVCL_9P37 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 98121502 | ECACC:98121502, Wikidata:Q54830702 |
CVCL_9P37 | 2026-08-29 04:25:27 | 0 | |||||
|
DD3287 Resource Report Resource Website |
ECACC Cat# 98102921, RRID:CVCL_9P25 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98102921 | ECACC:98102921, Wikidata:Q54830671 |
CVCL_9P25 | 2026-08-29 04:25:26 | 0 | |||||
|
DD3281 Resource Report Resource Website |
ECACC Cat# 98102915, RRID:CVCL_9P19 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98102915 | ECACC:98102915, Wikidata:Q54830665 |
CVCL_9P19 | 2026-08-29 04:25:25 | 0 | |||||
|
DD3303 Resource Report Resource Website |
ECACC Cat# 98111204, RRID:CVCL_9P28 | Homo sapiens (Human) | Fragile X syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98111204 | ECACC:98111204, Wikidata:Q54830682 |
CVCL_9P28 | 2026-08-29 04:25:26 | 0 | ||||
|
DD3293 Resource Report Resource Website |
ECACC Cat# 98103012, RRID:CVCL_9M84 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 98103012 | ECACC:98103012, Wikidata:Q54830677 |
CVCL_9M84 | 2026-08-29 04:25:26 | 0 | |||||
|
DD3459 Resource Report Resource Website |
ECACC Cat# 99090117, RRID:CVCL_9P70 | Homo sapiens (Human) | Karyotypic information: 46,XY,t(2;9)?(q34;p21.2); de novo (ECACC=99090117)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 99090117 | ECACC:99090117, Wikidata:Q54830753 |
CVCL_9P70 | 2026-08-29 04:25:30 | 0 | |||||
|
DD3417 Resource Report Resource Website |
ECACC Cat# 99060325, RRID:CVCL_9P60 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 99060325 | ECACC:99060325, Wikidata:Q54830735 |
CVCL_9P60 | 2026-08-29 04:25:28 | 0 | |||||
|
DD3344 Resource Report Resource Website |
ECACC Cat# 99010601, RRID:CVCL_9P38 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 99010601 | ECACC:99010601, Wikidata:Q54830706 |
CVCL_9P38 | 2026-08-29 04:25:28 | 0 | |||||
|
DD3422 Resource Report Resource Website |
ECACC Cat# 99060719, RRID:CVCL_9P64 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 99060719 | ECACC:99060719, Wikidata:Q54830742 |
CVCL_9P64 | 2026-08-29 04:25:28 | 0 | |||||
|
DD3373 Resource Report Resource Website |
ECACC Cat# 99031005, RRID:CVCL_9N02 | Homo sapiens (Human) | Prader-Willi syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 99031005 | ECACC:99031005, Wikidata:Q54830716 |
CVCL_9N02 | 2026-08-29 04:25:27 | 0 | ||||
|
DD3375 Resource Report Resource Website |
ECACC Cat# 99031814, RRID:CVCL_9P44 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 99031814 | ECACC:99031814, Wikidata:Q54830718 |
CVCL_9P44 | 2026-08-29 04:25:29 | 0 | |||||
|
DD3458 Resource Report Resource Website |
ECACC Cat# 99802743, RRID:CVCL_9N09 | Homo sapiens (Human) | Karyotypic information: 46,XY,inv(12)?(p11.21;q21.2); de novo (ECACC=99802743)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 99802743 | ECACC:99802743, Wikidata:Q54830752 |
CVCL_9N09 | 2026-08-29 04:25:28 | 0 |
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