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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 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM22979 Resource Report Resource Website |
Coriell Cat# GM22979, RRID:CVCL_5S47 | Homo sapiens (Human) | 1p36 deletion syndrome | PMID:23665875 | Transformed cell line | Female | Coriell | GM22979 | Coriell:GM22979, Wikidata:Q54852855 |
CVCL_5S47 | Cellosaurus | 2026-10-17 06:19:23 | 0 | ||||
|
GM22995 Resource Report Resource Website |
RRID:CVCL_5S52 | Homo sapiens (Human) | 1p36 deletion syndrome | PMID:23665875 | Transformed cell line | Male | Coriell:GM22995, Wikidata:Q54852860 |
CVCL_5S52 | Cellosaurus | 2026-10-17 06:19:23 | 0 | ||||||
|
GM22972 Resource Report Resource Website |
RRID:CVCL_5S44 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | Coriell:GM22972, Wikidata:Q54852846 |
CVCL_5S44 | Cellosaurus | 2026-10-17 06:19:23 | 0 | |||||||
|
GM23226 Resource Report Resource Website |
RRID:CVCL_F170 | Homo sapiens (Human) | Type 1 diabetes mellitus | Population: Native North American; Alaskan. | PMID:23665875 | Induced pluripotent stem cell | Female | GM23226*A | Coriell:GM23226, SKIP:SKIP000182, SKIP:SKIP004346, Wikidata:Q54852921 |
cvcl_8518 | CVCL_F170 | Cellosaurus | 2026-10-17 06:19:24 | 0 | |||
|
GM23262 Resource Report Resource Website |
RRID:CVCL_F177 | Homo sapiens (Human) | Becker's muscular dystrophy | Population: Caucasian. | PMID:23665875 | Induced pluripotent stem cell | Male | GM23262*A | Coriell:GM23262, SKIP:SKIP000187, SKIP:SKIP004351, Wikidata:Q54852945 |
cvcl_8521 | CVCL_F177 | Cellosaurus | 2026-10-17 06:19:25 | 0 | |||
|
GM23081 Resource Report Resource Website |
Coriell Cat# GM23081, RRID:CVCL_5S68 | Homo sapiens (Human) | Autism spectrum disorder |
PMID:23495136 PMID:23665875 |
Transformed cell line | Male | 801-010 LCL | Coriell | GM23081 | Coriell:GM23081, Wikidata:Q54852886 |
CVCL_5S68 | Cellosaurus | 2026-10-17 06:19:24 | 0 | |||
|
GM23225 Resource Report Resource Website 1+ mentions |
RRID:CVCL_F169 | Homo sapiens (Human) | Huntington's disease | PMID:23665875 | Induced pluripotent stem cell | Female | GM23225*B | Coriell:GM23225, SKIP:SKIP000181, SKIP:SKIP004345, Wikidata:Q54852920 |
cvcl_8519 | CVCL_F169 | Cellosaurus | 2026-10-17 06:19:24 | 1 | ||||
|
GM23235 Resource Report Resource Website |
Coriell Cat# GM23235, RRID:CVCL_5S79 | Homo sapiens (Human) | Autism spectrum disorder |
PMID:23495136 PMID:23665875 |
Transformed cell line | Male | 801-013 LCL | Coriell | GM23235 | Coriell:GM23235, Wikidata:Q54852926 |
CVCL_5S79 | Cellosaurus | 2026-10-17 06:19:24 | 0 | |||
|
GM23232 Resource Report Resource Website |
RRID:CVCL_F191 | Homo sapiens (Human) | Adenosine deaminase deficiency | Population: Caucasian. | PMID:23665875 | Induced pluripotent stem cell | Male | GM23232*A | BioSample:SAMN00806683, Coriell:GM23232, SKIP:SKIP000184, SKIP:SKIP004348, Wikidata:Q54852925 |
cvcl_8517 | CVCL_F191 | Cellosaurus | 2026-10-17 06:19:24 | 0 | |||
|
GM23125 Resource Report Resource Website |
Coriell Cat# GM23125, RRID:CVCL_5S75 | Homo sapiens (Human) | Autism spectrum disorder |
PMID:23495136 PMID:23665875 |
Transformed cell line | Female | 801-011 LCL | Coriell | GM23125 | Coriell:GM23125, Wikidata:Q54852899 |
CVCL_5S75 | Cellosaurus | 2026-10-17 06:19:24 | 0 | |||
|
GM23270 Resource Report Resource Website |
RRID:CVCL_5S86 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | Coriell:GM23270, Wikidata:Q54852957 |
CVCL_5S86 | Cellosaurus | 2026-10-17 06:19:25 | 0 | |||||||
|
GM23264 Resource Report Resource Website |
Coriell Cat# GM23264, RRID:CVCL_5S85 | Homo sapiens (Human) | Chromosome 15q11-q13 duplication syndrome |
PMID:23495136 PMID:23665875 |
Transformed cell line | Female | 801-015 LCL | Coriell | GM23264 | Coriell:GM23264, Wikidata:Q54852947 |
CVCL_5S85 | Cellosaurus | 2026-10-17 06:19:25 | 0 | |||
|
GM23226 Resource Report Resource Website |
Coriell Cat# GM23226, RRID:CVCL_F170 | Homo sapiens (Human) | Type 1 diabetes mellitus | Population: Native North American; Alaskan. | PMID:23665875 | Induced pluripotent stem cell | Female | GM23226*A | Coriell | GM23226 | Coriell:GM23226, SKIP:SKIP000182, SKIP:SKIP004346, Wikidata:Q54852921 |
cvcl_8518 | CVCL_F170 | Cellosaurus | 2026-10-17 06:19:24 | 0 | |
|
GM23354 Resource Report Resource Website |
RRID:CVCL_HK74 | Homo sapiens (Human) | Prader-Willi syndrome | PMID:23665875 | Transformed cell line | Male | Coriell:GM23354, Wikidata:Q54853016 |
CVCL_HK74 | Cellosaurus | 2026-10-17 06:19:26 | 0 | ||||||
|
GM23302 Resource Report Resource Website |
Coriell Cat# GM23302, RRID:CVCL_5S87 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | Coriell | GM23302 | Coriell:GM23302, Wikidata:Q54852981 |
CVCL_5S87 | Cellosaurus | 2026-10-17 06:19:25 | 0 | |||||
|
GM23336 Resource Report Resource Website |
Coriell Cat# GM23336, RRID:CVCL_U546 | Homo sapiens (Human) | Prader-Willi syndrome | PMID:23665875 | Transformed cell line | Female | Coriell | GM23336 | Coriell:GM23336, Wikidata:Q54853009 |
CVCL_U546 | Cellosaurus | 2026-10-17 06:19:26 | 0 | ||||
|
GM23337 Resource Report Resource Website |
RRID:CVCL_BV43 | Homo sapiens (Human) | Prader-Willi syndrome | PMID:23665875 | Transformed cell line | Male | Coriell:GM23337, Wikidata:Q54853010 |
CVCL_BV43 | Cellosaurus | 2026-10-17 06:19:26 | 0 | ||||||
|
GM20410 Resource Report Resource Website |
Coriell Cat# GM20410, RRID:CVCL_5R12 | Homo sapiens (Human) | Angelman syndrome | PMID:23665875 | Transformed cell line | Female | Coriell | GM20410 | CLO:CLO_0029515, Coriell:GM20410, Wikidata:Q54851012 |
CVCL_5R12 | Cellosaurus | 2026-10-17 06:18:34 | 0 | ||||
|
GM20419 Resource Report Resource Website |
RRID:CVCL_5R15 | Homo sapiens (Human) | Attention deficit hyperactivity disorder | Population: Caucasian. | PMID:23665875 | Transformed cell line | Male | CLO:CLO_0029508, Coriell:GM20419, Wikidata:Q54851020 |
CVCL_5R15 | Cellosaurus | 2026-10-17 06:18:34 | 0 | |||||
|
GM20435 Resource Report Resource Website |
Coriell Cat# GM20435, RRID:CVCL_5R17 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | Coriell | GM20435 | Coriell:GM20435, Wikidata:Q54851025 |
CVCL_5R17 | Cellosaurus | 2026-10-17 06:18:35 | 0 |
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