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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 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM01993 Resource Report Resource Website |
Coriell Cat# GM01993, RRID:CVCL_F023 | Homo sapiens (Human) | 47,XYY syndrome | PMID:6661932 | Finite cell line | Male | GM-1993, GM 1993 | Coriell | GM01993 | CLO:CLO_0032354, BioSample:SAMN00807358, Coriell:GM01993, Wikidata:Q54837219 |
CVCL_F023 | Cellosaurus | 2026-09-26 06:48:51 | 0 | |||
|
GM01997 Resource Report Resource Website |
RRID:CVCL_CZ12 | Homo sapiens (Human) | Adenosine deaminase deficiency | Population: African American. | Finite cell line | Male | GM-1997 | CLO:CLO_0032285, BioSample:SAMN00807364, Coriell:GM01997, Wikidata:Q54837222 |
CVCL_CZ12 | Cellosaurus | 2026-09-26 06:48:51 | 0 | |||||
|
GM01954 Resource Report Resource Website Discontinued |
RRID:CVCL_7345 | Homo sapiens (Human) | Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. |
PMID:16260726 PMID:20889555 PMID:29959025 |
Transformed cell line | Female | GM-1954, GM1954, GM01954A, GM01080, GM-1080, GM1080, GM17217 | CLO:CLO_0013887, CLO:CLO_0032337, BioSample:SAMN00807334, Coriell:GM01080, Coriell:GM01954, Coriell:GM17217, GEO:GSM569531, GEO:GSM596281, GEO:GSM596641, GEO:GSM924819, Wikidata:Q54837201 |
CVCL_7345 | Cellosaurus | 2026-09-26 06:48:51 | 0 | |||||
|
GM01958 Resource Report Resource Website |
RRID:CVCL_0M13 | Homo sapiens (Human) | Cystic fibrosis | Population: Caucasian. | Finite cell line | Male | GM-1958 | CLO:CLO_0032334, BioSample:SAMN00807338, Coriell:GM01958, Wikidata:Q54837205 |
CVCL_0M13 | Cellosaurus | 2026-09-26 06:48:51 | 0 | |||||
|
GM01929 Resource Report Resource Website |
RRID:CVCL_W661 | Homo sapiens (Human) | Hunter syndrome | Population: Caucasian; Italian. | PMID:34990619 | Finite cell line | Male | GM-1929, GM01929A | CLO:CLO_0032397, BioSample:SAMN00807319, Coriell:GM01929, Wikidata:Q54837191 |
CVCL_W661 | Cellosaurus | 2026-09-26 06:48:50 | 0 | ||||
|
GM01954 Resource Report Resource Website Discontinued |
Coriell Cat# GM17217, RRID:CVCL_7345 | Homo sapiens (Human) | Population: Caucasian., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. |
PMID:16260726 PMID:20889555 PMID:29959025 |
Transformed cell line | Female | GM-1954, GM1954, GM01954A, GM01080, GM-1080, GM1080, GM17217 | Coriell | GM17217 | CLO:CLO_0013887, CLO:CLO_0032337, BioSample:SAMN00807334, Coriell:GM01080, Coriell:GM01954, Coriell:GM17217, GEO:GSM569531, GEO:GSM596281, GEO:GSM596641, GEO:GSM924819, Wikidata:Q54837201 |
CVCL_7345 | Cellosaurus | 2026-09-26 06:48:51 | 0 | |||
|
GM01955 Resource Report Resource Website |
RRID:CVCL_F020 | Homo sapiens (Human) | Hepatocyte nuclear factor 4-alpha associated monogenic diabetes | Population: Caucasian., Part of: R-W pedigree MODY cell line collection. | PMID:8945471 | Finite cell line | Male | GM-1955 | CLO:CLO_0032338, Coriell:GM01955, Wikidata:Q54837202 |
CVCL_F020 | Cellosaurus | 2026-09-26 06:48:51 | 0 | ||||
|
GM02006 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM02006, RRID:CVCL_JB89 | Homo sapiens (Human) | Ehlers-Danlos syndrome, type II | Population: Caucasian. | Finite cell line | Male | GM-2006 | Coriell | GM02006 | Coriell:GM02006, Wikidata:Q54837231 |
CVCL_JB89 | Cellosaurus | 2026-09-26 06:48:51 | 0 | |||
|
GM01960 Resource Report Resource Website |
RRID:CVCL_M989 | Homo sapiens (Human) | Ataxia with isolated vitamin E deficiency | Population: Mexican., Part of: Human variation panel. |
PMID:6458814 PMID:7299037 |
Finite cell line | Female | GM-1960, GM 1960, GM17063 | CLO:CLO_0014560, CLO:CLO_0032344, BioSample:SAMN00807342, Coriell:GM01960, Coriell:GM17063, Wikidata:Q54837207 |
CVCL_M989 | Cellosaurus | 2026-09-26 06:48:51 | 0 | ||||
|
GM01989 Resource Report Resource Website Discontinued |
Coriell Cat# GM01076, RRID:CVCL_7346 | Homo sapiens (Human) | Population: Caucasian., Part of: Human variation panel. | PMID:62390 | Transformed cell line | Male | GM-1989, GM 1989, GM1989, GM01989A, GM01076, GM-1076, GM1076, GM18005 | Coriell | GM01076 | CLO:CLO_0015997, CLO:CLO_0032356, BioSample:SAMN00807354, Coriell:GM01076, Coriell:GM01989, Coriell:GM18005, Wikidata:Q54837217 |
CVCL_7346 | Cellosaurus | 2026-09-26 06:48:51 | 0 | |||
|
GM01930 Resource Report Resource Website Discontinued |
Coriell Cat# GM01930, RRID:CVCL_L967 | Homo sapiens (Human) | Transformed cell line | Female | GM-1930, GM01802, GM-1802 | Coriell | GM01930 | CLO:CLO_0032396, BioSample:SAMN00807320, Coriell:GM01802, Coriell:GM01930, Wikidata:Q54837192 |
CVCL_L967 | Cellosaurus | 2026-09-26 06:48:50 | 0 | |||||
|
GM01912 Resource Report Resource Website |
Coriell Cat# GM01912, RRID:CVCL_4E25 | Homo sapiens (Human) | Sea-blue histiocyte syndrome | Population: Caucasian. | Finite cell line | Female | GM-1912 | Coriell | GM01912 | CLO:CLO_0032386, BioSample:SAMN00807306, Coriell:GM01912, Wikidata:Q54837179 |
CVCL_4E25 | Cellosaurus | 2026-09-26 06:48:50 | 0 | |||
|
GM01986 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_JD67 | Homo sapiens (Human) | Finite cell line | Female | GM-1986 | Coriell:GM01986, Wikidata:Q54837216 |
CVCL_JD67 | Cellosaurus | 2026-09-26 06:48:51 | 0 | |||||||
|
GM02030 Resource Report Resource Website |
RRID:CVCL_X259 | Homo sapiens (Human) | Trisomy 8 | Population: Caucasian. |
PMID:6661932 PMID:23665875 |
Finite cell line | Male | GM-2030, GM 2030 | CLO:CLO_0032576, BioSample:SAMN00807404, Coriell:GM02030, Wikidata:Q54837249 |
CVCL_X259 | Cellosaurus | 2026-09-26 06:48:51 | 0 | ||||
|
GM02058 Resource Report Resource Website |
Coriell Cat# GM02058, RRID:CVCL_V466 | Homo sapiens (Human) | Down syndrome | Karyotypic information: 46,XX,i(21)(qter->q10::q10->qter) [13]; 46,XX [87] (Coriell=GM02058)., Population: Jewish; Ashkenazi. | Finite cell line | Female | GM-2058 | Coriell | GM02058 | CLO:CLO_0032534, BioSample:SAMN00807444, Coriell:GM02058, Wikidata:Q54837277 |
CVCL_V466 | Cellosaurus | 2026-09-26 06:48:52 | 0 | |||
|
GM02123 Resource Report Resource Website |
Coriell Cat# GM02123, RRID:CVCL_1H43 | Homo sapiens (Human) | Huntington's disease | Donor information: At sampling donor was not affected with Huntington disease but at 25% risk for disease., Population: Caucasian. | Finite cell line | Male | GM-2123 | Coriell | GM02123 | CLO:CLO_0031848, BioSample:SAMN00807496, Coriell:GM02123, Wikidata:Q54837307 |
CVCL_1H43 | Cellosaurus | 2026-09-26 06:48:52 | 0 | |||
|
GM02039 Resource Report Resource Website |
RRID:CVCL_CW69 | Homo sapiens (Human) | Schizophrenia | Population: Caucasian. | Finite cell line | Male | GM-2039 | CLO:CLO_0032555, BioSample:SAMN00807420, Coriell:GM02039, Wikidata:Q54837258 |
CVCL_CW69 | Cellosaurus | 2026-09-26 06:48:51 | 0 | |||||
|
GM02085 Resource Report Resource Website |
RRID:CVCL_U703 | Homo sapiens (Human) | Bloom syndrome | Donor information: From Bloom Syndrome Registry patient 53(StAs) (BSR53)., Population: Jewish; Ashkenazi. |
PMID:436333 PMID:908169 |
Finite cell line | Female | GM-2085 | CLO:CLO_0032511, BioSample:SAMN00807472, Coriell:GM02085, GEO:GSM1316975, GEO:GSM1317012, Wikidata:Q54837293 |
CVCL_U703 | Cellosaurus | 2026-09-26 06:48:52 | 0 | ||||
|
GM02079 Resource Report Resource Website 1+ mentions |
RRID:CVCL_1H41 | Homo sapiens (Human) | Huntington's disease | Population: Caucasian. | PMID:6220707 | Finite cell line | Female | GM-2079, GM 2079, GM02079A | CLO:CLO_0032509, BioSample:SAMN00807468, Coriell:GM02079, Wikidata:Q54837291 |
CVCL_1H41 | Cellosaurus | 2026-09-26 06:48:52 | 1 | ||||
|
GM02064 Resource Report Resource Website |
RRID:CVCL_M994 | Homo sapiens (Human) | Hereditary persistence of fetal hemoglobin | Population: Africans south of the Sahara., Part of: Human variation panel. |
PMID:6196781 PMID:7313555 |
Transformed cell line | Male | GM-2064, GM 2064, GM2064, GM02064A, GM17342 | CLO:CLO_0013747, CLO:CLO_0032529, BioSample:SAMN00807450, Coriell:GM02064, Coriell:GM17342, Wikidata:Q54837281 |
CVCL_M994 | Cellosaurus | 2026-09-26 06:48:52 | 0 |
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