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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM01801 Resource Report Resource Website |
RRID:CVCL_1D31 | Homo sapiens (Human) | Transformed cell line | Female | GM-1801 | CLO:CLO_0031034, BioSample:SAMN00807191, Coriell:GM01801, Wikidata:Q54837089 |
CVCL_1D31 | 2026-07-25 04:32:24 | 0 | |||||||
|
GM01791 Resource Report Resource Website |
RRID:CVCL_AN06 | Homo sapiens (Human) | Ehlers-Danlos syndrome, type VI | Population: Caucasian. | Finite cell line | Female | GM-1791 | CLO:CLO_0031024, BioSample:SAMN00807175, Coriell:GM01791, Wikidata:Q54837081 |
CVCL_AN06 | 2026-07-25 04:32:23 | 0 | |||||
|
GM01805 Resource Report Resource Website Discontinued |
Coriell Cat# GM17213, RRID:CVCL_7337 | Homo sapiens (Human) | Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. |
PMID:62390 PMID:16260726 PMID:20889555 PMID:29959025 |
Transformed cell line | Female | GM-1805, GM01805A, GM01073, GM-1073, GM17213 | Coriell | GM17213 | CLO:CLO_0013893, CLO:CLO_0031046, BioSample:SAMN00807195, Coriell:GM01073, Coriell:GM01805, Coriell:GM17213, GEO:GSM569542, GEO:GSM596277, GEO:GSM596638, GEO:GSM924815, Wikidata:Q54837091 |
CVCL_7337 | 2026-07-25 04:32:23 | 0 | |||
|
GM01803 Resource Report Resource Website |
Coriell Cat# GM01803, RRID:CVCL_1E87 | Homo sapiens (Human) | Transformed cell line | Female | GM-1803 | Coriell | GM01803 | CLO:CLO_0031032, BioSample:SAMN00807193, Coriell:GM01803, Wikidata:Q54837090 |
CVCL_1E87 | 2026-07-25 04:32:24 | 0 | |||||
|
GM01786 Resource Report Resource Website |
RRID:CVCL_0G94 | Homo sapiens (Human) | Finite cell line | Female | GM-1786 | CLO:CLO_0031011, BioSample:SAMN00807165, Coriell:GM01786, Wikidata:Q54837076 |
CVCL_0G94 | 2026-07-25 04:32:23 | 0 | |||||||
|
GM01777 Resource Report Resource Website |
RRID:CVCL_AA17 | Homo sapiens (Human) | Familial dysautonomia | Transformed cell line | Female | GM-1777, GM01777A | CLO:CLO_0031014, BioSample:SAMN00807157, Coriell:GM01777, Wikidata:Q54837069 |
CVCL_AA17 | 2026-07-25 04:32:25 | 0 | ||||||
|
GM01827 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM01827, RRID:CVCL_JE13 | Homo sapiens (Human) | Schizophrenia | Transformed cell line | Female | GM-1827 | Coriell | GM01827 | Coriell:GM01827, Wikidata:Q54837107 |
CVCL_JE13 | 2026-07-25 04:32:24 | 0 | ||||
|
GM01785 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_JE08 | Homo sapiens (Human) | Metachromatic leukodystrophy | Transformed cell line | Female | GM-1785 | Coriell:GM01785, Wikidata:Q54837075 |
CVCL_JE08 | 2026-07-25 04:32:25 | 0 | ||||||
|
GM01778 Resource Report Resource Website |
Coriell Cat# GM01778, RRID:CVCL_1K53 | Homo sapiens (Human) | Transformed cell line | Female | GM-1778 | Coriell | GM01778 | CLO:CLO_0031018, BioSample:SAMN00807159, Coriell:GM01778, Wikidata:Q54837070 |
CVCL_1K53 | 2026-07-25 04:32:25 | 0 | |||||
|
GM01812 Resource Report Resource Website |
Coriell Cat# GM01812, RRID:CVCL_AM82 | Homo sapiens (Human) | Ehlers-Danlos syndrome, type I | Finite cell line | Female | GM-1812 | Coriell | GM01812 | CLO:CLO_0031044, Coriell:GM01812, Wikidata:Q54837100 |
CVCL_AM82 | 2026-07-25 04:32:24 | 0 | ||||
|
GM01799 Resource Report Resource Website |
RRID:CVCL_1D29 | Homo sapiens (Human) | Wolfram syndrome | Transformed cell line | Female | GM-1799 | CLO:CLO_0031039, BioSample:SAMN00807187, Coriell:GM01799, Wikidata:Q54837087 |
CVCL_1D29 | 2026-07-25 04:32:25 | 0 | ||||||
|
GM01789 Resource Report Resource Website |
RRID:CVCL_DD68 | Homo sapiens (Human) | Osteogenesis imperfecta | Population: Caucasian. | Finite cell line | Female | GM-1789 | CLO:CLO_0031010, BioSample:SAMN00807171, Coriell:GM01789, Wikidata:Q54837079 |
CVCL_DD68 | 2026-07-25 04:32:25 | 0 | |||||
|
GM01812 Resource Report Resource Website |
RRID:CVCL_AM82 | Homo sapiens (Human) | Ehlers-Danlos syndrome, type I | Finite cell line | Female | GM-1812 | CLO:CLO_0031044, Coriell:GM01812, Wikidata:Q54837100 |
CVCL_AM82 | 2026-07-25 04:32:24 | 0 | ||||||
|
GM01767 Resource Report Resource Website Discontinued |
Coriell Cat# GM01452, RRID:CVCL_L963 | Homo sapiens (Human) | Hyperlipoproteinemia, type IIa | Transformed cell line | Female | GM-1767, GM01452, GM-1452 | Coriell | GM01452 | CLO:CLO_0031000, Coriell:GM01452, Coriell:GM01767, Wikidata:Q54837064 |
CVCL_L963 | 2026-07-25 04:32:22 | 0 | ||||
|
GM01751 Resource Report Resource Website |
Coriell Cat# GM01751, RRID:CVCL_0Q58 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(9;14)(9qter->9p24::14q21->14qter;14pter->14q21::9p24->9pter) (Coriell=GM01751)., Population: Caucasian. | Finite cell line | Female | GM-1751 | Coriell | GM01751 | CLO:CLO_0031005, BioSample:SAMN00807141, Coriell:GM01751, Wikidata:Q54837060 |
CVCL_0Q58 | 2026-07-25 04:32:23 | 0 | ||||
|
GM01790 Resource Report Resource Website |
Coriell Cat# GM01790, RRID:CVCL_AN05 | Homo sapiens (Human) | Ehlers-Danlos syndrome, type VI | Population: Caucasian. | Finite cell line | Female | GM-1790 | Coriell | GM01790 | CLO:CLO_0031013, BioSample:SAMN00807173, Coriell:GM01790, Wikidata:Q54837080 |
CVCL_AN05 | 2026-07-25 04:32:25 | 0 | |||
|
GM01879 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM01879, RRID:CVCL_DF18 | Homo sapiens (Human) | Retinoblastoma |
PMID:7253718 PMID:7471105 |
Finite cell line | Female | GM-1879, GM01879A, AG01879, AG-1879, AG 1879, AG1879 | Coriell | GM01879 | CLO:CLO_0032408, BioSample:SAMN00807268, Coriell:AG01879, Coriell:GM01879, Wikidata:Q54837154 |
CVCL_DF18 | 2026-07-25 04:32:26 | 0 | |||
|
GM01905 Resource Report Resource Website |
RRID:CVCL_GR94 | Homo sapiens (Human) | Type 1 diabetes mellitus | Transformed cell line | Female | GM-1905 | CLO:CLO_0032372, Coriell:GM01905, Wikidata:Q54837172 |
CVCL_GR94 | 2026-07-25 04:32:26 | 0 | ||||||
|
GM01838 Resource Report Resource Website |
RRID:CVCL_AI31 | Homo sapiens (Human) | Hepatocyte nuclear factor 4-alpha associated monogenic diabetes | Population: Caucasian., Part of: R-W pedigree MODY cell line collection. | PMID:8945471 | Transformed cell line | Female | GM-1838 | CLO:CLO_0031413, Coriell:GM01838, Wikidata:Q54837115 |
CVCL_AI31 | 2026-07-25 04:32:25 | 0 | ||||
|
GM01878 Resource Report Resource Website |
RRID:CVCL_CY05 | Homo sapiens (Human) | Population: Caucasian. |
PMID:7438795 PMID:24555846 |
Finite cell line | Female | GM-1878, GM1878 | CLO:CLO_0032406, BioSample:SAMN00807266, Coriell:GM01878, GEO:GSM1288435, Wikidata:Q54837153 |
CVCL_CY05 | 2026-07-25 04:32:26 | 0 |
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