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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
DD0126 Resource Report Resource Website |
ECACC Cat# 90122403, RRID:CVCL_8U77 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 90122403 | ECACC:90122403, Wikidata:Q54828765 |
CVCL_8U77 | 2026-08-15 04:26:13 | 0 | |||||
|
DD0128 Resource Report Resource Website |
ECACC Cat# 90122405, RRID:CVCL_8U79 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 90122405 | ECACC:90122405, Wikidata:Q54828767 |
CVCL_8U79 | 2026-08-15 04:26:11 | 0 | |||||
|
DD0116 Resource Report Resource Website |
ECACC Cat# 89112412, RRID:CVCL_8U74 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 89112412 | ECACC:89112412, Wikidata:Q54828761 |
CVCL_8U74 | 2026-08-15 04:26:13 | 0 | |||||
|
DD0071 Resource Report Resource Website |
ECACC Cat# 90060403, RRID:CVCL_8U57 | Homo sapiens (Human) | Karyotypic information: 46,XX; 47,XX,+i(12p) (ECACC=90060403)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 90060403 | ECACC:90060403, Wikidata:Q54828742 |
CVCL_8U57 | 2026-08-15 04:26:11 | 0 | |||||
|
DD0175 Resource Report Resource Website |
ECACC Cat# 91020801, RRID:CVCL_8V00 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91020801 | ECACC:91020801, Wikidata:Q54828800 |
CVCL_8V00 | 2026-08-15 04:26:14 | 0 | |||||
|
DD0179 Resource Report Resource Website |
ECACC Cat# 91021504, RRID:CVCL_8V03 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91021504 | ECACC:91021504, Wikidata:Q54828803 |
CVCL_8V03 | 2026-08-15 04:26:14 | 0 | |||||
|
DD0171 Resource Report Resource Website |
ECACC Cat# 91020711, RRID:CVCL_8U97 | Homo sapiens (Human) | Fragile X syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91020711 | ECACC:91020711, Wikidata:Q54828797 |
CVCL_8U97 | 2026-08-15 04:26:13 | 0 | ||||
|
DD0147 Resource Report Resource Website |
ECACC Cat# 91011611, RRID:CVCL_8U90 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91011611 | ECACC:91011611, Wikidata:Q54828779 |
CVCL_8U90 | 2026-08-15 04:26:12 | 0 | |||||
|
DD0220 Resource Report Resource Website |
ECACC Cat# 91032116, RRID:CVCL_8V30 | Homo sapiens (Human) | Karyotypic information: 46,X,del(X)(pter->q22.3::q26.1->qter) (ECACC=91032116)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91032116 | ECACC:91032116, Wikidata:Q54828831 |
CVCL_8V30 | 2026-08-15 04:26:15 | 0 | |||||
|
DD0186 Resource Report Resource Website |
ECACC Cat# 91022220, RRID:CVCL_8V08 | Homo sapiens (Human) | Karyotypic information: 46,XY,?dup(1)(q32->q42.1) (ECACC=91022220)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 91022220 | ECACC:91022220, Wikidata:Q54828808 |
CVCL_8V08 | 2026-08-15 04:26:12 | 0 | |||||
|
DD0223 Resource Report Resource Website |
ECACC Cat# 91032713, RRID:CVCL_8V32 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91032713 | ECACC:91032713, Wikidata:Q54828833 |
CVCL_8V32 | 2026-08-15 04:26:13 | 0 | |||||
|
DD0184 Resource Report Resource Website |
ECACC Cat# 91022218, RRID:CVCL_8V06 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91022218 | ECACC:91022218, Wikidata:Q54828806 |
CVCL_8V06 | 2026-08-15 04:26:14 | 0 | |||||
|
DD0176 Resource Report Resource Website |
ECACC Cat# 91021302, RRID:CVCL_8V01 | Homo sapiens (Human) | Karyotypic information: 46,XY,t(3;18)(p21.31;q23)mat (ECACC=91021302)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 91021302 | ECACC:91021302, Wikidata:Q54828801 |
CVCL_8V01 | 2026-08-15 04:26:12 | 0 | |||||
|
DD0172 Resource Report Resource Website |
ECACC Cat# 91020712, RRID:CVCL_8U98 | Homo sapiens (Human) | Fragile X syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91020712 | ECACC:91020712, Wikidata:Q54828798 |
CVCL_8U98 | 2026-08-15 04:26:12 | 0 | ||||
|
DD0173 Resource Report Resource Website |
ECACC Cat# 880928011, RRID:CVCL_8U99 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 880928011 | ECACC:880928011, Wikidata:Q54828799 |
CVCL_8U99 | 2026-08-15 04:26:12 | 0 | |||||
|
DD0207 Resource Report Resource Website |
ECACC Cat# 91031817, RRID:CVCL_8V24 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91031817 | ECACC:91031817, Wikidata:Q54828825 |
CVCL_8V24 | 2026-08-15 04:26:14 | 0 | |||||
|
DD0228 Resource Report Resource Website |
ECACC Cat# 91032718, RRID:CVCL_8V36 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91032718 | ECACC:91032718, Wikidata:Q54828847 |
CVCL_8V36 | 2026-08-15 04:26:15 | 0 | |||||
|
DD0153 Resource Report Resource Website |
ECACC Cat# 91012606, RRID:CVCL_8U93 | Homo sapiens (Human) | Fragile X syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91012606 | ECACC:91012606, Wikidata:Q54828782 |
CVCL_8U93 | 2026-08-15 04:26:12 | 0 | ||||
|
DD0195 Resource Report Resource Website |
ECACC Cat# 91030608, RRID:CVCL_8V14 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 91030608 | ECACC:91030608, Wikidata:Q54828814 |
CVCL_8V14 | 2026-08-15 04:26:13 | 0 | |||||
|
DD0154 Resource Report Resource Website |
ECACC Cat# 91012607, RRID:CVCL_8U94 | Homo sapiens (Human) | Karyotypic information: 46,XX,var(13p) (ECACC=91012607)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 91012607 | ECACC:91012607, Wikidata:Q54828783 |
CVCL_8U94 | 2026-08-15 04:26:12 | 0 |
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