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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM23502 Resource Report Resource Website |
Coriell Cat# GM23502, RRID:CVCL_Y728 | Homo sapiens (Human) | Ornithine carbamoyltransferase deficiency disease | Transformed cell line | Female | Coriell | GM23502 | Coriell:GM23502, Wikidata:Q54853123 |
CVCL_Y728 | 2026-09-03 06:37:17 | 0 | |||||
|
GM23634 Resource Report Resource Website |
RRID:CVCL_BV92 | Homo sapiens (Human) | Rett syndrome | Part of: Genetic Testing Reference Material (GeT-RM) samples. | PMID:24508304 | Transformed cell line | Female | Coriell:GM23634, Wikidata:Q54853171 |
CVCL_BV92 | 2026-09-03 06:37:19 | 0 | |||||
|
GM23620 Resource Report Resource Website |
RRID:CVCL_1N03 | Homo sapiens (Human) | Transformed cell line | Female | Coriell:GM23620, Wikidata:Q54853157 |
CVCL_1N03 | 2026-09-03 06:37:18 | 0 | ||||||||
|
GM23490 Resource Report Resource Website |
Coriell Cat# GM23490, RRID:CVCL_1K32 | Homo sapiens (Human) | Charcot-Marie-Tooth disease type 1A | Transformed cell line | Female | Coriell | GM23490 | Coriell:GM23490, Wikidata:Q54853110 |
CVCL_1K32 | 2026-09-03 06:37:18 | 0 | |||||
|
GM23613 Resource Report Resource Website |
Coriell Cat# GM23613, RRID:CVCL_M919 | Homo sapiens (Human) | Hardcastle's syndrome | Finite cell line | Female | Coriell | GM23613 | Coriell:GM23613, Wikidata:Q54853152 |
CVCL_M919 | 2026-09-03 06:37:19 | 0 | |||||
|
GM23501 Resource Report Resource Website |
RRID:CVCL_Y727 | Homo sapiens (Human) | Transformed cell line | Female | Coriell:GM23501, Wikidata:Q54853122 |
CVCL_Y727 | 2026-09-03 06:37:18 | 0 | ||||||||
|
GM23610 Resource Report Resource Website |
Coriell Cat# GM23610, RRID:CVCL_1N01 | Homo sapiens (Human) | Hardcastle's syndrome | Transformed cell line | Female | Coriell | GM23610 | Coriell:GM23610, Wikidata:Q54853149 |
CVCL_1N01 | 2026-09-03 06:37:19 | 0 | |||||
|
GM23629 Resource Report Resource Website |
Coriell Cat# GM23629, RRID:CVCL_GS99 | Homo sapiens (Human) | Oculopharyngeal muscular dystrophy | Transformed cell line | Female | Coriell | GM23629 | Coriell:GM23629, Wikidata:Q54853166 |
CVCL_GS99 | 2026-09-03 06:37:19 | 0 | |||||
|
GM23495 Resource Report Resource Website |
RRID:CVCL_4F83 | Homo sapiens (Human) | Medium-chain acyl-CoA dehydrogenase deficiency | Transformed cell line | Female | Coriell:GM23495, Wikidata:Q54853115 |
CVCL_4F83 | 2026-09-03 06:37:17 | 0 | |||||||
|
GM23605 Resource Report Resource Website |
RRID:CVCL_BV84 | Homo sapiens (Human) | Rett syndrome | Part of: Genetic Testing Reference Material (GeT-RM) samples. | PMID:24508304 | Transformed cell line | Female | Coriell:GM23605, Wikidata:Q54853144 |
CVCL_BV84 | 2026-09-03 06:37:18 | 0 | |||||
|
GM23611 Resource Report Resource Website |
Coriell Cat# GM23611, RRID:CVCL_1N02 | Homo sapiens (Human) | Hardcastle's syndrome | Finite cell line | Female | Coriell | GM23611 | Coriell:GM23611, Wikidata:Q54853150 |
CVCL_1N02 | 2026-09-03 06:37:18 | 0 | |||||
|
GM23497 Resource Report Resource Website |
Coriell Cat# GM23497, RRID:CVCL_BV77 | Homo sapiens (Human) | Rett syndrome | Transformed cell line | Female | Coriell | GM23497 | Coriell:GM23497, Wikidata:Q54853118 |
CVCL_BV77 | 2026-09-03 06:37:18 | 0 | |||||
|
GM23498 Resource Report Resource Website |
RRID:CVCL_5S94 | Homo sapiens (Human) | Argininosuccinic aciduria | PMID:23665875 | Transformed cell line | Female | Coriell:GM23498, Wikidata:Q54853119 |
CVCL_5S94 | 2026-09-03 06:37:18 | 0 | ||||||
|
GM23499 Resource Report Resource Website |
Coriell Cat# GM23499, RRID:CVCL_CX80 | Homo sapiens (Human) | Transformed cell line | Female | Coriell | GM23499 | Coriell:GM23499, Wikidata:Q54853120 |
CVCL_CX80 | 2026-09-03 06:37:17 | 0 | ||||||
|
GM23692 Resource Report Resource Website |
RRID:CVCL_1L25 | Homo sapiens (Human) | Glycogen storage disease type V | Transformed cell line | Female | Coriell:GM23692, Wikidata:Q54853233 |
CVCL_1L25 | 2026-09-03 06:37:20 | 0 | |||||||
|
GM23697 Resource Report Resource Website |
RRID:CVCL_5T03 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | Coriell:GM23697, Wikidata:Q54853242 |
CVCL_5T03 | 2026-09-03 06:37:19 | 0 | |||||||
|
GM23720 Resource Report Resource Website |
Coriell Cat# GM23720, RRID:CVCL_T818 | Homo sapiens (Human) | Population: Caucasian. | Induced pluripotent stem cell | Female | GM23720*B | Coriell | GM23720 | Coriell:GM23720, SKIP:SKIP000259, SKIP:SKIP004368, Wikidata:Q54853264 |
cvcl_7355 | CVCL_T818 | 2026-09-03 06:37:20 | 0 | |||
|
GM23657 Resource Report Resource Website |
RRID:CVCL_Y737 | Homo sapiens (Human) | Transformed cell line | Female | Coriell:GM23657, Wikidata:Q54853203 |
CVCL_Y737 | 2026-09-03 06:37:19 | 0 | ||||||||
|
GM23702 Resource Report Resource Website |
Coriell Cat# GM23702, RRID:CVCL_5T08 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | Coriell | GM23702 | Coriell:GM23702, Wikidata:Q54853247 |
CVCL_5T08 | 2026-09-03 06:37:19 | 0 | |||||
|
GM23708 Resource Report Resource Website |
Coriell Cat# GM23708, RRID:CVCL_5T11 | Homo sapiens (Human) | Chromosome 15q11-q13 duplication syndrome | PMID:23665875 | Transformed cell line | Female | Coriell | GM23708 | Coriell:GM23708, Wikidata:Q54853253 |
CVCL_5T11 | 2026-09-03 06:37:19 | 0 |
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