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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM23694 Resource Report Resource Website |
RRID:CVCL_5T00 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | Coriell:GM23694, Wikidata:Q54853235 |
CVCL_5T00 | 2026-02-14 08:20:29 | 0 | |||||||
|
GM23676 Resource Report Resource Website |
RRID:CVCL_5S98 | Homo sapiens (Human) | Lubs X-linked intellectual disability syndrome | Part of: Genetic Testing Reference Material (GeT-RM) samples. |
PMID:23665875 PMID:24508304 |
Transformed cell line | Female | Coriell:GM23676, Wikidata:Q54853219 |
CVCL_5S98 | 2026-02-14 08:20:29 | 0 | |||||
|
GM23711 Resource Report Resource Website |
RRID:CVCL_5T12 | Homo sapiens (Human) | Intellectual developmental disorder, autosomal dominant 1 | PMID:23665875 | Transformed cell line | Female | Coriell:GM23711, Wikidata:Q54853256 |
CVCL_5T12 | 2026-02-14 08:20:30 | 0 | ||||||
|
GM23813 Resource Report Resource Website |
RRID:CVCL_5T18 | Homo sapiens (Human) | Chromosome 15q11-q13 duplication syndrome | PMID:23665875 | Transformed cell line | Male | Coriell:GM23813, Wikidata:Q54853325 |
CVCL_5T18 | 2026-02-14 08:20:32 | 0 | ||||||
|
GM23723 Resource Report Resource Website |
RRID:CVCL_5T17 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | Coriell:GM23723, Wikidata:Q54853267 |
CVCL_5T17 | 2026-02-14 08:20:30 | 0 | |||||||
|
GM23813 Resource Report Resource Website |
Coriell Cat# GM23813, RRID:CVCL_5T18 | Homo sapiens (Human) | Chromosome 15q11-q13 duplication syndrome | PMID:23665875 | Transformed cell line | Male | Coriell | GM23813 | Coriell:GM23813, Wikidata:Q54853325 |
CVCL_5T18 | 2026-02-14 08:20:32 | 0 | ||||
|
GM23881 Resource Report Resource Website |
Coriell Cat# GM23881, RRID:CVCL_5T29 | Homo sapiens (Human) |
PMID:23665875 PMID:26621101 |
Transformed cell line | Male | Coriell | GM23881 | Coriell:GM23881, Wikidata:Q54853415 |
CVCL_5T29 | 2026-02-14 08:20:33 | 0 | |||||
|
GM23863 Resource Report Resource Website |
RRID:CVCL_U554 | Homo sapiens (Human) | Prader-Willi syndrome | PMID:23665875 | Transformed cell line | Male | Coriell:GM23863, Wikidata:Q54853385 |
CVCL_U554 | 2026-02-14 08:20:33 | 0 | ||||||
|
GM23830 Resource Report Resource Website |
RRID:CVCL_5T21 | Homo sapiens (Human) | Isodicentric chromosome | PMID:23665875 | Transformed cell line | Female | Coriell:GM23830, Wikidata:Q54853358 |
CVCL_5T21 | 2026-02-14 08:20:32 | 0 | ||||||
|
GM23899 Resource Report Resource Website |
RRID:CVCL_U555 | Homo sapiens (Human) | Prader-Willi syndrome | PMID:23665875 | Transformed cell line | Male | Coriell:GM23899, Wikidata:Q54853428 |
CVCL_U555 | 2026-02-14 08:20:34 | 0 | ||||||
|
GM23854 Resource Report Resource Website |
Coriell Cat# GM23854, RRID:CVCL_5T23 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | Coriell | GM23854 | Coriell:GM23854, Wikidata:Q54853378 |
CVCL_5T23 | 2026-02-14 08:20:33 | 0 | |||||
|
GM23857 Resource Report Resource Website |
RRID:CVCL_U552 | Homo sapiens (Human) | Prader-Willi syndrome | PMID:23665875 | Transformed cell line | Male | Coriell:GM23857, Wikidata:Q54853380 |
CVCL_U552 | 2026-02-14 08:20:33 | 0 | ||||||
|
GM23854 Resource Report Resource Website |
RRID:CVCL_5T23 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | Coriell:GM23854, Wikidata:Q54853378 |
CVCL_5T23 | 2026-02-14 08:20:33 | 0 | |||||||
|
GM23832 Resource Report Resource Website |
Coriell Cat# GM23832, RRID:CVCL_U550 | Homo sapiens (Human) | Prader-Willi syndrome | PMID:23665875 | Transformed cell line | Female | Coriell | GM23832 | Coriell:GM23832, Wikidata:Q54853361 |
CVCL_U550 | 2026-02-14 08:20:32 | 0 | ||||
|
GM23873 Resource Report Resource Website |
Coriell Cat# GM23873, RRID:CVCL_5T25 | Homo sapiens (Human) |
PMID:23665875 PMID:26621101 PMID:29474986 |
Transformed cell line | Female | Coriell | GM23873 | Coriell:GM23873, Wikidata:Q54853409 |
CVCL_5T25 | 2026-02-14 08:20:33 | 0 | |||||
|
GM23862 Resource Report Resource Website |
RRID:CVCL_U553 | Homo sapiens (Human) | Prader-Willi syndrome | PMID:23665875 | Transformed cell line | Female | Coriell:GM23862, Wikidata:Q54853384 |
CVCL_U553 | 2026-02-14 08:20:33 | 0 | ||||||
|
GM23922 Resource Report Resource Website |
RRID:CVCL_5T38 | Homo sapiens (Human) | Hyperglycerolemia | PMID:23665875 | Transformed cell line | Male | Coriell:GM23922, Wikidata:Q54853442 |
CVCL_5T38 | 2026-02-14 08:20:34 | 0 | ||||||
|
GM23905 Resource Report Resource Website |
Coriell Cat# GM23905, RRID:CVCL_5T32 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | Coriell | GM23905 | Coriell:GM23905, Wikidata:Q54853431 |
CVCL_5T32 | 2026-02-14 08:20:34 | 0 | |||||
|
GM23906 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_5T33 | Homo sapiens (Human) | Hyperglycerolemia | PMID:23665875 | Transformed cell line | Male | Coriell:GM23906, Wikidata:Q54853432 |
CVCL_5T33 | 2026-02-14 08:20:34 | 0 | ||||||
|
GM23900 Resource Report Resource Website |
Coriell Cat# GM23900, RRID:CVCL_5T30 | Homo sapiens (Human) | Turner syndrome | PMID:23665875 | Transformed cell line | Female | Coriell | GM23900 | Coriell:GM23900, Wikidata:Q54853429 |
CVCL_5T30 | 2026-02-14 08:20:34 | 0 |
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