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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
DD3033 Resource Report Resource Website |
ECACC Cat# 98010201, RRID:CVCL_9L97 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98010201 | ECACC:98010201, Wikidata:Q54830530 |
CVCL_9L97 | 2026-08-29 04:25:22 | 0 | ||||
|
DD3066 Resource Report Resource Website |
ECACC Cat# 98030404, RRID:CVCL_9M04 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 98030404 | ECACC:98030404, Wikidata:Q54830539 |
CVCL_9M04 | 2026-08-29 04:25:22 | 0 | |||||
|
DD3048 Resource Report Resource Website |
ECACC Cat# 98012702, RRID:CVCL_9M02 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98012702 | ECACC:98012702, Wikidata:Q54830537 |
CVCL_9M02 | 2026-08-29 04:25:21 | 0 | ||||
|
DD3012 Resource Report Resource Website |
ECACC Cat# 97112203, RRID:CVCL_9L91 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97112203 | ECACC:97112203, Wikidata:Q54830515 |
CVCL_9L91 | 2026-08-29 04:25:22 | 0 | |||||
|
DD3030 Resource Report Resource Website |
ECACC Cat# 97122306, RRID:CVCL_9L95 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 97122306 | ECACC:97122306, Wikidata:Q54830527 |
CVCL_9L95 | 2026-08-29 04:25:22 | 0 | ||||
|
DD2997 Resource Report Resource Website |
ECACC Cat# 97102401, RRID:CVCL_9L85 | Homo sapiens (Human) | Karyotypic information: 46,XY,inv(7)(p12.2;p21.3)pat (ECACC=97102401)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 97102401 | ECACC:97102401, Wikidata:Q54830506 |
CVCL_9L85 | 2026-08-29 04:25:21 | 0 | |||||
|
DD2996 Resource Report Resource Website |
ECACC Cat# 97102306, RRID:CVCL_9L84 | Homo sapiens (Human) | Karyotypic information: 46,XY.ish 22q11.2(cH748X2) (ECACC=97102306)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 97102306 | ECACC:97102306, Wikidata:Q54830505 |
CVCL_9L84 | 2026-08-29 04:25:20 | 0 | |||||
|
DD3073 Resource Report Resource Website |
ECACC Cat# 98031003, RRID:CVCL_9M09 | Homo sapiens (Human) | Karyotypic information: 46,XY,t(1;8)(p32;q13); de novo (ECACC=98031003)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 98031003 | ECACC:98031003, Wikidata:Q54830544 |
CVCL_9M09 | 2026-08-29 04:25:21 | 0 | |||||
|
DD3127 Resource Report Resource Website |
ECACC Cat# 980427187, RRID:CVCL_9M38 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 980427187 | ECACC:980427187, Wikidata:Q54830580 |
CVCL_9M38 | 2026-08-29 04:25:23 | 0 | ||||
|
DD3088 Resource Report Resource Website |
ECACC Cat# 98032403, RRID:CVCL_9M21 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 98032403 | ECACC:98032403, Wikidata:Q54830556 |
CVCL_9M21 | 2026-08-29 04:25:22 | 0 | |||||
|
DD3076 Resource Report Resource Website |
ECACC Cat# 98031011, RRID:CVCL_9M11 | Homo sapiens (Human) | Goldenhar syndrome | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 98031011 | ECACC:98031011, Wikidata:Q54830546 |
CVCL_9M11 | 2026-08-29 04:25:22 | 0 | ||||
|
DD3090 Resource Report Resource Website |
ECACC Cat# 98032405, RRID:CVCL_9M23 | Homo sapiens (Human) | Karyotypic information: 47,XXY,t(3;4)(q26.32;q31.1)mat (ECACC=98032405)., Part of: ECACC chromosomal abnormality collection. | Finite cell line | Sex ambiguous | ECACC | 98032405 | ECACC:98032405, Wikidata:Q54830558 |
CVCL_9M23 | 2026-08-29 04:25:22 | 0 | |||||
|
DD3154 Resource Report Resource Website |
ECACC Cat# 98052032, RRID:CVCL_9N79 | Homo sapiens (Human) | Karyotypic information: 46,X,del(X)(p11.2) (ECACC=98052032)., Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98052032 | ECACC:98052032, Wikidata:Q54830592 |
CVCL_9N79 | 2026-08-29 04:25:23 | 0 | |||||
|
DD3117 Resource Report Resource Website |
ECACC Cat# 98042201, RRID:CVCL_9M36 | Homo sapiens (Human) | Type 1 diabetes mellitus | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98042201 | ECACC:98042201, Wikidata:Q54830576 |
CVCL_9M36 | 2026-08-29 04:25:22 | 0 | ||||
|
DD3130 Resource Report Resource Website |
ECACC Cat# 98050116, RRID:CVCL_9M41 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Male | ECACC | 98050116 | ECACC:98050116, Wikidata:Q54830583 |
CVCL_9M41 | 2026-08-29 04:25:23 | 0 | |||||
|
DD3156 Resource Report Resource Website |
ECACC Cat# 98052033, RRID:CVCL_9N80 | Homo sapiens (Human) | Fragile X syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98052033 | ECACC:98052033, Wikidata:Q54830593 |
CVCL_9N80 | 2026-08-29 04:25:24 | 0 | ||||
|
DD3168 Resource Report Resource Website |
ECACC Cat# 98061112, RRID:CVCL_9M50 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Female | ECACC | 98061112 | ECACC:98061112, Wikidata:Q54830594 |
CVCL_9M50 | 2026-08-29 04:25:23 | 0 | |||||
|
DD3145 Resource Report Resource Website |
ECACC Cat# 98050515, RRID:CVCL_9M48 | Homo sapiens (Human) | Part of: ECACC chromosomal abnormality collection. | Finite cell line | Male | ECACC | 98050515 | ECACC:98050515, Wikidata:Q54830590 |
CVCL_9M48 | 2026-08-29 04:25:24 | 0 | |||||
|
DD3128 Resource Report Resource Website |
ECACC Cat# 98042906, RRID:CVCL_9M39 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98042906 | ECACC:98042906, Wikidata:Q54830581 |
CVCL_9M39 | 2026-08-29 04:25:24 | 0 | ||||
|
DD3132 Resource Report Resource Website |
ECACC Cat# 98050123, RRID:CVCL_9M43 | Homo sapiens (Human) | Turner syndrome | Part of: ECACC chromosomal abnormality collection. | Transformed cell line | Female | ECACC | 98050123 | ECACC:98050123, Wikidata:Q54830585 |
CVCL_9M43 | 2026-08-29 04:25:23 | 0 |
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