Searching the RRID Resource Information Network
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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 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM16808 Resource Report Resource Website |
Coriell Cat# GM16808, RRID:CVCL_5Q79 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | Coriell | GM16808 | Coriell:GM16808, Wikidata:Q54848755 |
CVCL_5Q79 | Cellosaurus | 2026-10-24 05:30:51 | 0 | |||||
|
GM16994 Resource Report Resource Website |
RRID:CVCL_2N34 | Homo sapiens (Human) | Autism spectrum disorder | PMID:23665875 | Transformed cell line | Male | Coriell:GM16994, Wikidata:Q54848827 |
CVCL_2N34 | Cellosaurus | 2026-10-24 05:30:51 | 0 | ||||||
|
GM17867 Resource Report Resource Website |
RRID:CVCL_W965 | Homo sapiens (Human) | Klinefelter syndrome | PMID:23665875 | Transformed cell line | Male | CLO:CLO_0016462, Coriell:GM17867, Wikidata:Q54849292 |
CVCL_W965 | Cellosaurus | 2026-10-24 05:30:58 | 0 | ||||||
|
GM22439 Resource Report Resource Website |
Coriell Cat# GM22439, RRID:CVCL_5M61 | Homo sapiens (Human) | Jacobsen syndrome | PMID:23665875 | Transformed cell line | Female | Coriell | GM22439 | Coriell:GM22439, Wikidata:Q54852567 |
CVCL_5M61 | Cellosaurus | 2026-10-24 05:32:07 | 0 | ||||
|
GM22421 Resource Report Resource Website |
RRID:CVCL_5M60 | Homo sapiens (Human) | Jacobsen syndrome | PMID:23665875 | Transformed cell line | Male | Coriell:GM22421, Wikidata:Q54852566 |
CVCL_5M60 | Cellosaurus | 2026-10-24 05:32:07 | 0 | ||||||
|
GM22364 Resource Report Resource Website |
RRID:CVCL_5R61 | Homo sapiens (Human) | Chromosome 15q11-q13 duplication syndrome |
PMID:23495136 PMID:23665875 |
Transformed cell line | Male | 801-005 LCL | Coriell:GM22364, Wikidata:Q54852542 |
CVCL_5R61 | Cellosaurus | 2026-10-24 05:32:06 | 0 | |||||
|
GM22569 Resource Report Resource Website |
Coriell Cat# GM22569, RRID:CVCL_5R82 | Homo sapiens (Human) | 1p36 deletion syndrome | PMID:23665875 | Transformed cell line | Female | Coriell | GM22569 | Coriell:GM22569, Wikidata:Q54852629 |
CVCL_5R82 | Cellosaurus | 2026-10-24 05:32:08 | 0 | ||||
|
GM22601 Resource Report Resource Website |
RRID:CVCL_V824 | Homo sapiens (Human) | Wolf-Hirschhorn syndrome | PMID:23665875 | Transformed cell line | Male | Coriell:GM22601, Wikidata:Q54852650 |
CVCL_V824 | Cellosaurus | 2026-10-24 05:32:09 | 0 | ||||||
|
GM22626 Resource Report Resource Website |
RRID:CVCL_1K39 | Homo sapiens (Human) | Potocki-Shaffer syndrome | PMID:23665875 | Transformed cell line | Male | Coriell:GM22626, Wikidata:Q54852667 |
CVCL_1K39 | Cellosaurus | 2026-10-24 05:32:09 | 0 | ||||||
|
GM22634 Resource Report Resource Website |
Coriell Cat# GM22634, RRID:CVCL_5R93 | Homo sapiens (Human) | Primary open angle glaucoma | Population: Caucasian. | PMID:23665875 | Transformed cell line | Female | Coriell | GM22634 | Coriell:GM22634, Wikidata:Q54852677 |
CVCL_5R93 | Cellosaurus | 2026-10-24 05:32:09 | 0 | |||
|
GM22569 Resource Report Resource Website |
RRID:CVCL_5R82 | Homo sapiens (Human) | 1p36 deletion syndrome | PMID:23665875 | Transformed cell line | Female | Coriell:GM22569, Wikidata:Q54852629 |
CVCL_5R82 | Cellosaurus | 2026-10-24 05:32:08 | 0 | ||||||
|
GM22623 Resource Report Resource Website |
RRID:CVCL_1K36 | Homo sapiens (Human) | Karyotypic information: 46,XX,ins(13;11)(q14.1;p11.2p12).ish ins(13;11)(q14.1;p11.2p12)(wcp11+).arr(1-22,X)x2 (Coriell=GM22623). | PMID:23665875 | Transformed cell line | Female | Coriell:GM22623, Wikidata:Q54852664 |
CVCL_1K36 | Cellosaurus | 2026-10-24 05:32:09 | 0 | ||||||
|
GM22634 Resource Report Resource Website |
RRID:CVCL_5R93 | Homo sapiens (Human) | Primary open angle glaucoma | Population: Caucasian. | PMID:23665875 | Transformed cell line | Female | Coriell:GM22634, Wikidata:Q54852677 |
CVCL_5R93 | Cellosaurus | 2026-10-24 05:32:09 | 0 | |||||
|
GM22593 Resource Report Resource Website |
RRID:CVCL_5R86 | Homo sapiens (Human) | Autism spectrum disorder |
PMID:23495136 PMID:23665875 |
Transformed cell line | Female | 801-009 LCL | Coriell:GM22593, Wikidata:Q54852642 |
CVCL_5R86 | Cellosaurus | 2026-10-24 05:32:09 | 0 | |||||
|
GM22630 Resource Report Resource Website |
RRID:CVCL_1K43 | Homo sapiens (Human) | Potocki-Shaffer syndrome | PMID:23665875 | Transformed cell line | Female | Coriell:GM22630, Wikidata:Q54852671 |
CVCL_1K43 | Cellosaurus | 2026-10-24 05:32:09 | 0 | ||||||
|
GM22629 Resource Report Resource Website |
Coriell Cat# GM22629, RRID:CVCL_1K42 | Homo sapiens (Human) | Potocki-Shaffer syndrome | PMID:23665875 | Transformed cell line | Female | Coriell | GM22629 | Coriell:GM22629, Wikidata:Q54852670 |
CVCL_1K42 | Cellosaurus | 2026-10-24 05:32:09 | 0 | ||||
|
GM22627 Resource Report Resource Website |
RRID:CVCL_1K40 | Homo sapiens (Human) | Potocki-Shaffer syndrome | PMID:23665875 | Transformed cell line | Male | Coriell:GM22627, Wikidata:Q54852668 |
CVCL_1K40 | Cellosaurus | 2026-10-24 05:32:09 | 0 | ||||||
|
GM22622 Resource Report Resource Website |
RRID:CVCL_N354 | Homo sapiens (Human) | Potocki-Shaffer syndrome | Population: Mexican. | PMID:23665875 | Transformed cell line | Female | Coriell:GM22622, Wikidata:Q54852663 |
CVCL_N354 | Cellosaurus | 2026-10-24 05:32:09 | 0 | |||||
|
GM22571 Resource Report Resource Website |
Coriell Cat# GM22571, RRID:CVCL_5R84 | Homo sapiens (Human) | Autism spectrum disorder |
PMID:23495136 PMID:23665875 |
Transformed cell line | Male | 801-007 LCL | Coriell | GM22571 | Coriell:GM22571, Wikidata:Q54852631 |
CVCL_5R84 | Cellosaurus | 2026-10-24 05:32:08 | 0 | |||
|
GM22627 Resource Report Resource Website |
Coriell Cat# GM22627, RRID:CVCL_1K40 | Homo sapiens (Human) | Potocki-Shaffer syndrome | PMID:23665875 | Transformed cell line | Male | Coriell | GM22627 | Coriell:GM22627, Wikidata:Q54852668 |
CVCL_1K40 | Cellosaurus | 2026-10-24 05:32:09 | 0 |
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