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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM50275 Resource Report Resource Website |
RRID:CVCL_5T61 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | Coriell:GM50275, Wikidata:Q54854262 |
CVCL_5T61 | 2026-09-12 05:37:48 | 0 | |||||||
|
GM50178 Resource Report Resource Website |
Coriell Cat# GM50178, RRID:CVCL_0G67 | Homo sapiens (Human) | Cri du chat syndrome | PMID:23665875 | Transformed cell line | Female | JL378 | Coriell | GM50178 | CLO:CLO_0014986, Coriell:GM50178, Wikidata:Q54854249 |
CVCL_0G67 | 2026-09-12 05:37:48 | 0 | |||
|
GM50322 Resource Report Resource Website |
RRID:CVCL_1U17 | Homo sapiens (Human) | Deletion 18p syndrome |
PMID:1577474 PMID:23665875 |
Transformed cell line | Female | JL91 | CLO:CLO_0012521, Coriell:GM50322, Wikidata:Q54854268 |
CVCL_1U17 | 2026-09-12 05:37:48 | 0 | |||||
|
GM50323 Resource Report Resource Website |
Coriell Cat# GM50323, RRID:CVCL_1U18 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | JL92 | Coriell | GM50323 | CLO:CLO_0012520, Coriell:GM50323, Wikidata:Q54854269 |
CVCL_1U18 | 2026-09-12 05:37:49 | 0 | ||||
|
GM02003 Resource Report Resource Website |
RRID:CVCL_X085 | Homo sapiens (Human) | Population: Caucasian. |
PMID:6617268 PMID:6661932 PMID:23665875 |
Finite cell line | Female | GM-2003, GM 2003 | CLO:CLO_0032295, BioSample:SAMN00807372, Coriell:GM02003, Wikidata:Q54837229 |
CVCL_X085 | 2026-09-12 05:32:07 | 0 | |||||
|
GM02003 Resource Report Resource Website |
Coriell Cat# GM02003, RRID:CVCL_X085 | Homo sapiens (Human) | Population: Caucasian. |
PMID:6617268 PMID:6661932 PMID:23665875 |
Finite cell line | Female | GM-2003, GM 2003 | Coriell | GM02003 | CLO:CLO_0032295, BioSample:SAMN00807372, Coriell:GM02003, Wikidata:Q54837229 |
CVCL_X085 | 2026-09-12 05:32:07 | 0 | |||
|
GM01921 Resource Report Resource Website |
Coriell Cat# GM01921, RRID:CVCL_V465 | Homo sapiens (Human) | Down syndrome | Population: Caucasian. |
PMID:6617268 PMID:23665875 |
Transformed cell line | Male | GM-1921, GM 1921, GM01921A | Coriell | GM01921 | CLO:CLO_0032392, BioSample:SAMN00807314, Coriell:GM01921, Wikidata:Q54837187 |
CVCL_V465 | 2026-09-12 05:32:06 | 0 | ||
|
GM02008 Resource Report Resource Website |
RRID:CVCL_X086 | Homo sapiens (Human) | Population: African American. |
PMID:6617268 PMID:6661932 PMID:23665875 |
Finite cell line | Female | GM-2008, GM 2008 | CLO:CLO_0032298, BioSample:SAMN00807378, Coriell:GM02008, Wikidata:Q54837233 |
CVCL_X086 | 2026-09-12 05:32:07 | 0 | |||||
|
GM01921 Resource Report Resource Website |
RRID:CVCL_V465 | Homo sapiens (Human) | Down syndrome | Population: Caucasian. |
PMID:6617268 PMID:23665875 |
Transformed cell line | Male | GM-1921, GM 1921, GM01921A | CLO:CLO_0032392, BioSample:SAMN00807314, Coriell:GM01921, Wikidata:Q54837187 |
CVCL_V465 | 2026-09-12 05:32:06 | 0 | ||||
|
GM01941 Resource Report Resource Website |
RRID:CVCL_X084 | Homo sapiens (Human) | Turner syndrome | Population: Caucasian. |
PMID:6617268 PMID:6661932 PMID:23665875 |
Finite cell line | Female | GM-1941, GM 1941 | CLO:CLO_0032323, BioSample:SAMN00807328, Coriell:GM01941, Wikidata:Q54837198 |
CVCL_X084 | 2026-09-12 05:32:06 | 0 | ||||
|
GM02030 Resource Report Resource Website |
Coriell Cat# GM02030, RRID:CVCL_X259 | Homo sapiens (Human) | Trisomy 8 | Population: Caucasian. |
PMID:6661932 PMID:23665875 |
Finite cell line | Male | GM-2030, GM 2030 | Coriell | GM02030 | CLO:CLO_0032576, BioSample:SAMN00807404, Coriell:GM02030, Wikidata:Q54837249 |
CVCL_X259 | 2026-09-12 05:32:08 | 0 | ||
|
GM02025 Resource Report Resource Website |
Coriell Cat# GM02025, RRID:CVCL_V825 | Homo sapiens (Human) | Population: Caucasian. |
PMID:6617268 PMID:6661932 PMID:23665875 |
Finite cell line | Male | GM-2025, GM 2025, GM2025 | Coriell | GM02025 | CLO:CLO_0032577, BioSample:SAMN00807400, Coriell:GM02025, Wikidata:Q54837244 |
CVCL_V825 | 2026-09-12 05:32:08 | 0 | |||
|
GM02325 Resource Report Resource Website |
RRID:CVCL_X262 | Homo sapiens (Human) | Karyotypic information: 47,XX,+der(22)(22pter->22q11.21::16p13.11->16pter)mat (Coriell=GM02325)., Population: Caucasian. |
PMID:6661932 PMID:23665875 |
Finite cell line | Female | GM-2325, GM 2325 | CLO:CLO_0032174, BioSample:SAMN00807695, Coriell:GM02325, Wikidata:Q54837427 |
CVCL_X262 | 2026-09-12 05:32:12 | 0 | |||||
|
GM02205 Resource Report Resource Website Discontinued |
RRID:CVCL_L968 | Homo sapiens (Human) | Population: Caucasian. |
PMID:6617268 PMID:23665875 PMID:24555846 PMID:25326100 |
Finite cell line | Male | GM-2205, GM 2205, GM01515 | CLO:CLO_0032263, BioSample:SAMN00807602, Coriell:GM01515, Coriell:GM02205, GEO:GSM1266975, GEO:GSM1267054, GEO:GSM1288438, Wikidata:Q54837369 |
CVCL_L968 | 2026-09-12 05:32:10 | 0 | |||||
|
GM02205 Resource Report Resource Website Discontinued |
Coriell Cat# GM01515, RRID:CVCL_L968 | Homo sapiens (Human) | Population: Caucasian. |
PMID:6617268 PMID:23665875 PMID:24555846 PMID:25326100 |
Finite cell line | Male | GM-2205, GM 2205, GM01515 | Coriell | GM01515 | CLO:CLO_0032263, BioSample:SAMN00807602, Coriell:GM01515, Coriell:GM02205, GEO:GSM1266975, GEO:GSM1267054, GEO:GSM1288438, Wikidata:Q54837369 |
CVCL_L968 | 2026-09-12 05:32:10 | 0 | |||
|
GM02325 Resource Report Resource Website |
Coriell Cat# GM02325, RRID:CVCL_X262 | Homo sapiens (Human) | Karyotypic information: 47,XX,+der(22)(22pter->22q11.21::16p13.11->16pter)mat (Coriell=GM02325)., Population: Caucasian. |
PMID:6661932 PMID:23665875 |
Finite cell line | Female | GM-2325, GM 2325 | Coriell | GM02325 | CLO:CLO_0032174, BioSample:SAMN00807695, Coriell:GM02325, Wikidata:Q54837427 |
CVCL_X262 | 2026-09-12 05:32:12 | 0 | |||
|
GM02298 Resource Report Resource Website |
RRID:CVCL_5M71 | Homo sapiens (Human) | Becker's muscular dystrophy | Part of: Genetic Testing Reference Material (GeT-RM) samples. |
PMID:6093571 PMID:21354051 PMID:23665875 |
Finite cell line | Male | GM-2298, GM2298, GM02298A, HF-B | CLO:CLO_0032205, Coriell:GM02298, Wikidata:Q54837412 |
CVCL_5M71 | 2026-09-12 05:32:11 | 0 | ||||
|
GM02206 Resource Report Resource Website Discontinued |
RRID:CVCL_L969 | Homo sapiens (Human) | Ehlers-Danlos syndrome | Population: Caucasian. |
PMID:6617268 PMID:23665875 PMID:25326100 |
Finite cell line | Female | GM-2206 GM 2206, GM01514 | CLO:CLO_0032262, BioSample:SAMN00807604, Coriell:GM01514, Coriell:GM02206, GEO:GSM1266977, Wikidata:Q54837370 |
CVCL_L969 | 2026-09-12 05:32:10 | 0 | ||||
|
GM02365 Resource Report Resource Website |
RRID:CVCL_1R62 | Homo sapiens (Human) | Coffin-Lowry syndrome | Population: Caucasian. | PMID:23665875 | Finite cell line | Male | GM02365A | CLO:CLO_0033101, BioSample:SAMN00807737, Coriell:GM02365, Wikidata:Q54837463 |
CVCL_1R62 | 2026-09-12 05:32:13 | 0 | ||||
|
GM02365 Resource Report Resource Website |
Coriell Cat# GM02365, RRID:CVCL_1R62 | Homo sapiens (Human) | Coffin-Lowry syndrome | Population: Caucasian. | PMID:23665875 | Finite cell line | Male | GM02365A | Coriell | GM02365 | CLO:CLO_0033101, BioSample:SAMN00807737, Coriell:GM02365, Wikidata:Q54837463 |
CVCL_1R62 | 2026-09-12 05:32:13 | 0 |
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