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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM05152 Resource Report Resource Website |
RRID:CVCL_AW59 | Homo sapiens (Human) | Dystrophia myotonica 1 | Population: Caucasian., Part of: Genetic Testing Reference Material (GeT-RM) samples. | PMID:23680132 | Transformed cell line | Male | CLO:CLO_0025246, Coriell:GM05152, Wikidata:Q54838890 |
CVCL_AW59 | 2026-08-08 05:00:24 | 0 | |||||
|
GM05091 Resource Report Resource Website |
Coriell Cat# GM05091, RRID:CVCL_DS13 | Homo sapiens (Human) | Ichthyosis | Population: Caucasian; Sardinian. | Finite cell line | Male | Coriell | GM05091 | CLO:CLO_0025320, Coriell:GM05091, Wikidata:Q54838850 |
CVCL_DS13 | 2026-08-08 05:00:23 | 0 | ||||
|
GM05123 Resource Report Resource Website |
RRID:CVCL_5N16 | Homo sapiens (Human) | Duchenne muscular dystrophy | Population: Caucasian. | Finite cell line | Male | CLO:CLO_0025369, Coriell:GM05123, Wikidata:Q54838870 |
CVCL_5N16 | 2026-08-08 05:00:23 | 0 | ||||||
|
GM05142 Resource Report Resource Website |
Coriell Cat# GM05142, RRID:CVCL_AW57 | Homo sapiens (Human) | Dystrophia myotonica 1 | Population: Caucasian. | Finite cell line | Male | Coriell | GM05142 | CLO:CLO_0025243, Coriell:GM05142, Wikidata:Q54838883 |
CVCL_AW57 | 2026-08-08 05:00:24 | 0 | ||||
|
GM05147 Resource Report Resource Website |
RRID:CVCL_1K23 | Homo sapiens (Human) | Charcot-Marie-Tooth disease type 1A | Population: Caucasian. | Transformed cell line | Female | CLO:CLO_0025240, Coriell:GM05147, Wikidata:Q54838886 |
CVCL_1K23 | 2026-08-08 05:00:23 | 0 | ||||||
|
GM05109 Resource Report Resource Website |
RRID:CVCL_AA56 | Homo sapiens (Human) | Population: Jewish; Ashkenazi. | Transformed cell line | Female | CLO:CLO_0025319, Coriell:GM05109, Wikidata:Q54838857 |
CVCL_AA56 | 2026-08-08 05:00:22 | 0 | |||||||
|
GM05112 Resource Report Resource Website |
RRID:CVCL_5N08 | Homo sapiens (Human) | Duchenne muscular dystrophy | Population: Caucasian. | PMID:23665875 | Finite cell line | Male | CLO:CLO_0025379, Coriell:GM05112, Wikidata:Q54838862 |
CVCL_5N08 | 2026-08-08 05:00:24 | 0 | |||||
|
GM05184 Resource Report Resource Website |
RRID:CVCL_1Q25 | Homo sapiens (Human) | Karyotypic information: 46,XY,t(6;7)(6pter->6q21::7q21.2->7qter;7pter->7q21.2::6q21->6qter) (Coriell=GM05184)., Population: Caucasian; Italian. | Transformed cell line | Male | CLO:CLO_0025284, Coriell:GM05184, Wikidata:Q54838915 |
CVCL_1Q25 | 2026-08-08 05:00:25 | 0 | |||||||
|
GM05185 Resource Report Resource Website |
RRID:CVCL_AX80 | Homo sapiens (Human) | Fragile X syndrome | Population: Caucasian. | Finite cell line | Male | CLO:CLO_0025297, Coriell:GM05185, Wikidata:Q54838917 |
CVCL_AX80 | 2026-08-08 05:00:24 | 0 | ||||||
|
GM05119 Resource Report Resource Website |
Coriell Cat# GM05119, RRID:CVCL_5N15 | Homo sapiens (Human) | Population: Caucasian. | Transformed cell line | Male | Coriell | GM05119 | CLO:CLO_0025371, Coriell:GM05119, Wikidata:Q54838869 |
CVCL_5N15 | 2026-08-08 05:00:24 | 0 | |||||
|
GM05181 Resource Report Resource Website |
Coriell Cat# GM05181, RRID:CVCL_DD78 | Homo sapiens (Human) | Osteogenesis imperfecta type I | Population: Caucasian. | Finite cell line | Male | Coriell | GM05181 | CLO:CLO_0025280, Coriell:GM05181, Wikidata:Q54838912 |
CVCL_DD78 | 2026-08-08 05:00:23 | 0 | ||||
|
GM05091 Resource Report Resource Website |
RRID:CVCL_DS13 | Homo sapiens (Human) | Ichthyosis | Population: Caucasian; Sardinian. | Finite cell line | Male | CLO:CLO_0025320, Coriell:GM05091, Wikidata:Q54838850 |
CVCL_DS13 | 2026-08-08 05:00:22 | 0 | ||||||
|
GM05133 Resource Report Resource Website |
Coriell Cat# GM05133, RRID:CVCL_X317 | Homo sapiens (Human) | Karyotypic information: 46,XY,der(14)(14qter->14p11.2::20p11.1->20pter)mat (Coriell=GM05133)., Population: African American. | PMID:6661932 | Finite cell line | Male | GM 5133 | Coriell | GM05133 | CLO:CLO_0025354, Coriell:GM05133, Wikidata:Q54838880 |
CVCL_X317 | 2026-08-08 05:00:24 | 0 | |||
|
GM05167 Resource Report Resource Website |
Coriell Cat# GM05167, RRID:CVCL_1K28 | Homo sapiens (Human) | Charcot-Marie-Tooth disease type 1A | Population: Caucasian. | Finite cell line | Female | Coriell | GM05167 | CLO:CLO_0025263, Coriell:GM05167, Wikidata:Q54838902 |
CVCL_1K28 | 2026-08-08 05:00:23 | 0 | ||||
|
GM05208 Resource Report Resource Website |
Coriell Cat# GM05208, RRID:CVCL_AW62 | Homo sapiens (Human) | Dystrophia myotonica 1 | Population: Caucasian. | Finite cell line | Male | Coriell | GM05208 | CLO:CLO_0025298, Coriell:GM05208, Wikidata:Q54838918 |
CVCL_AW62 | 2026-08-08 05:00:24 | 0 | ||||
|
GM05156 Resource Report Resource Website |
Coriell Cat# GM05156, RRID:CVCL_4F91 | Homo sapiens (Human) | Bipolar disorder | Population: Caucasian. | Transformed cell line | Female | GM5156, GM05156A | Coriell | GM05156 | CLO:CLO_0025247, Coriell:GM05156, Wikidata:Q54838891 |
CVCL_4F91 | 2026-08-08 05:00:23 | 0 | |||
|
GM05167 Resource Report Resource Website |
RRID:CVCL_1K28 | Homo sapiens (Human) | Charcot-Marie-Tooth disease type 1A | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0025263, Coriell:GM05167, Wikidata:Q54838902 |
CVCL_1K28 | 2026-08-08 05:00:23 | 0 | ||||||
|
GM05174 Resource Report Resource Website |
Coriell Cat# GM05174, RRID:CVCL_5N30 | Homo sapiens (Human) | Transformed cell line | Female | Coriell | GM05174 | CLO:CLO_0025279, Coriell:GM05174, Wikidata:Q54838911 |
CVCL_5N30 | 2026-08-08 05:00:23 | 0 | ||||||
|
GM05183 Resource Report Resource Website |
RRID:CVCL_1Q24 | Homo sapiens (Human) | Karyotypic information: 46,XY,t(6;7)(q21;q21.2) (Coriell=GM05183)., Population: Caucasian; Italian. | Finite cell line | Male | GM05183A | CLO:CLO_0025283, Coriell:GM05183, Wikidata:Q54838914 |
CVCL_1Q24 | 2026-08-08 05:00:23 | 0 | ||||||
|
GM05125 Resource Report Resource Website |
RRID:CVCL_5N18 | Homo sapiens (Human) | Duchenne muscular dystrophy | Population: Caucasian. | Finite cell line | Male | CLO:CLO_0025356, Coriell:GM05125, Wikidata:Q54838872 |
CVCL_5N18 | 2026-08-08 05:00:24 | 0 |
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