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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM23941 Resource Report Resource Website |
RRID:CVCL_BW28 | Homo sapiens (Human) | Rett syndrome | Transformed cell line | Female | Coriell:GM23941, Wikidata:Q54853455 |
CVCL_BW28 | 2026-09-05 10:59:43 | 0 | |||||||
|
GM23945 Resource Report Resource Website |
RRID:CVCL_CX82 | Homo sapiens (Human) | Population: Caucasian. | Finite cell line | Female | Coriell:GM23945, Wikidata:Q54853459 |
CVCL_CX82 | 2026-09-05 10:59:43 | 0 | |||||||
|
GM24019 Resource Report Resource Website |
RRID:CVCL_Y779 | Homo sapiens (Human) | Ornithine carbamoyltransferase deficiency disease | Transformed cell line | Female | Coriell:GM24019, Wikidata:Q54853491 |
CVCL_Y779 | 2026-09-05 10:59:44 | 0 | |||||||
|
GM24010 Resource Report Resource Website |
RRID:CVCL_Y775 | Homo sapiens (Human) | Ornithine carbamoyltransferase deficiency disease | Population: Caucasian; Greek/Portuguese. | Transformed cell line | Female | Coriell:GM24010, Wikidata:Q54853487 |
CVCL_Y775 | 2026-09-05 10:59:44 | 0 | ||||||
|
GM24018 Resource Report Resource Website |
Coriell Cat# GM24018, RRID:CVCL_Y778 | Homo sapiens (Human) | Ornithine carbamoyltransferase deficiency disease | Transformed cell line | Female | Coriell | GM24018 | Coriell:GM24018, Wikidata:Q54853490 |
CVCL_Y778 | 2026-09-05 10:59:44 | 0 | |||||
|
GM23926 Resource Report Resource Website |
RRID:CVCL_BX15 | Homo sapiens (Human) | Central core disease | Transformed cell line | Female | Coriell:GM23926, Wikidata:Q54853452 |
CVCL_BX15 | 2026-09-05 10:59:43 | 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 | 2026-09-05 10:59:42 | 0 | |||||
|
GM24010 Resource Report Resource Website |
Coriell Cat# GM24010, RRID:CVCL_Y775 | Homo sapiens (Human) | Ornithine carbamoyltransferase deficiency disease | Population: Caucasian; Greek/Portuguese. | Transformed cell line | Female | Coriell | GM24010 | Coriell:GM24010, Wikidata:Q54853487 |
CVCL_Y775 | 2026-09-05 10:59:44 | 0 | ||||
|
GM23919 Resource Report Resource Website |
RRID:CVCL_4F85 | Homo sapiens (Human) | Medium-chain acyl-CoA dehydrogenase deficiency | Transformed cell line | Female | Coriell:GM23919, Wikidata:Q54853440 |
CVCL_4F85 | 2026-09-05 10:59:42 | 0 | |||||||
|
GM24011 Resource Report Resource Website |
RRID:CVCL_Y776 | Homo sapiens (Human) | Ornithine carbamoyltransferase deficiency disease | Population: Caucasian; Portuguese. | Transformed cell line | Female | Coriell:GM24011, Wikidata:Q54853488 |
CVCL_Y776 | 2026-09-05 10:59:44 | 0 | ||||||
|
GM23944 Resource Report Resource Website |
Coriell Cat# GM23944, RRID:CVCL_BW29 | Homo sapiens (Human) | Rett syndrome | Transformed cell line | Female | Coriell | GM23944 | Coriell:GM23944, Wikidata:Q54853458 |
CVCL_BW29 | 2026-09-05 10:59:43 | 0 | |||||
|
GM24011 Resource Report Resource Website |
Coriell Cat# GM24011, RRID:CVCL_Y776 | Homo sapiens (Human) | Ornithine carbamoyltransferase deficiency disease | Population: Caucasian; Portuguese. | Transformed cell line | Female | Coriell | GM24011 | Coriell:GM24011, Wikidata:Q54853488 |
CVCL_Y776 | 2026-09-05 10:59:44 | 0 | ||||
|
GM24019 Resource Report Resource Website |
Coriell Cat# GM24019, RRID:CVCL_Y779 | Homo sapiens (Human) | Ornithine carbamoyltransferase deficiency disease | Transformed cell line | Female | Coriell | GM24019 | Coriell:GM24019, Wikidata:Q54853491 |
CVCL_Y779 | 2026-09-05 10:59:44 | 0 | |||||
|
GM24017 Resource Report Resource Website |
Coriell Cat# GM24017, RRID:CVCL_Y777 | Homo sapiens (Human) | Ornithine carbamoyltransferase deficiency disease | Transformed cell line | Female | Coriell | GM24017 | Coriell:GM24017, Wikidata:Q54853489 |
CVCL_Y777 | 2026-09-05 10:59:44 | 0 | |||||
|
GM23941 Resource Report Resource Website |
Coriell Cat# GM23941, RRID:CVCL_BW28 | Homo sapiens (Human) | Rett syndrome | Transformed cell line | Female | Coriell | GM23941 | Coriell:GM23941, Wikidata:Q54853455 |
CVCL_BW28 | 2026-09-05 10:59:43 | 0 | |||||
|
GM24017 Resource Report Resource Website |
RRID:CVCL_Y777 | Homo sapiens (Human) | Ornithine carbamoyltransferase deficiency disease | Transformed cell line | Female | Coriell:GM24017, Wikidata:Q54853489 |
CVCL_Y777 | 2026-09-05 10:59:44 | 0 | |||||||
|
GM23943 Resource Report Resource Website |
RRID:CVCL_U556 | Homo sapiens (Human) | Prader-Willi syndrome | Transformed cell line | Female | Coriell:GM23943, Wikidata:Q54853457 |
CVCL_U556 | 2026-09-05 10:59:43 | 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 | 2026-09-05 10:59:42 | 0 | ||||
|
GM23905 Resource Report Resource Website |
RRID:CVCL_5T32 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | Coriell:GM23905, Wikidata:Q54853431 |
CVCL_5T32 | 2026-09-05 10:59:42 | 0 | |||||||
|
GM23944 Resource Report Resource Website |
RRID:CVCL_BW29 | Homo sapiens (Human) | Rett syndrome | Transformed cell line | Female | Coriell:GM23944, Wikidata:Q54853458 |
CVCL_BW29 | 2026-09-05 10:59:43 | 0 |
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