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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM01835 Resource Report Resource Website 1+ mentions |
RRID:CVCL_D873 | Homo sapiens (Human) | Schizophrenia | Population: Jewish and Caucasian; Scandinavian. |
PMID:7847674 PMID:21490598 |
Finite cell line | Female | GM-1835 | CLO:CLO_0031421, BioSample:SAMN00807213, Coriell:GM01835, Wikidata:Q54837112 |
CVCL_D873 | 2026-09-19 05:27:10 | 1 | ||||
|
GM01981 Resource Report Resource Website 1+ mentions |
RRID:CVCL_F589 | Homo sapiens (Human) | Menkes disease | Population: Caucasian. |
PMID:7438975 PMID:7977350 |
Finite cell line | Male | GM-1981, GM1981 | CLO:CLO_0032339, BioSample:SAMN00807346, Coriell:GM01981, Wikidata:Q54837212 |
CVCL_F589 | 2026-09-19 05:27:13 | 1 | ||||
|
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 | 2026-09-19 05:27:14 | 1 | ||||
|
GM02075 Resource Report Resource Website 1+ mentions |
RRID:CVCL_CW70 | Homo sapiens (Human) | Chediak-Higashi syndrome | Population: Caucasian. |
PMID:8896560 PMID:36259166 |
Finite cell line | Female | GM-2075, GM02075A | CLO:CLO_0032513, BioSample:SAMN00807462, Coriell:GM02075, Wikidata:Q54837288 |
CVCL_CW70 | 2026-09-19 05:27:14 | 1 | ||||
|
GM02036 Resource Report Resource Website 1+ mentions |
Coriell Cat# GM02036, RRID:CVCL_7348 | Homo sapiens (Human) | Population: Caucasian. |
PMID:17668376 PMID:28284873 PMID:29125828 PMID:32291635 PMID:33038742 PMID:35850241 |
Finite cell line | Female | GM2036, GM 02036, GM-02036, GM-2036, GM02036A, GMO2036A, C2036 | Coriell | GM02036 | CLO:CLO_0032573, BioSample:SAMN00807414, BioSample:SAMN03253067, Coriell:GM02036, GEO:GSM2794402, Wikidata:Q54837255 |
CVCL_7348 | 2026-09-19 05:27:13 | 4 | |||
|
GM02036 Resource Report Resource Website 1+ mentions |
RRID:CVCL_7348 | Homo sapiens (Human) | Population: Caucasian. |
PMID:17668376 PMID:28284873 PMID:29125828 PMID:32291635 PMID:33038742 PMID:35850241 |
Finite cell line | Female | GM2036, GM 02036, GM-02036, GM-2036, GM02036A, GMO2036A, C2036 | CLO:CLO_0032573, BioSample:SAMN00807414, BioSample:SAMN03253067, Coriell:GM02036, GEO:GSM2794402, Wikidata:Q54837255 |
CVCL_7348 | 2026-09-19 05:27:13 | 4 | |||||
|
GM06097 Resource Report Resource Website 1+ mentions |
RRID:CVCL_5U20 | Homo sapiens (Human) | Miller-Dieker syndrome | Population: Caucasian. |
PMID:23665875 PMID:24413397 |
Finite cell line | Female | GM06097A, MDS2 Fib | CLO:CLO_0023619, Coriell:GM06097, Wikidata:Q54842162 |
CVCL_5U20 | 2026-09-19 05:28:04 | 1 | ||||
|
GM06144 Resource Report Resource Website 1+ mentions |
RRID:CVCL_X456 | Homo sapiens (Human) | Wolman disease | Population: Caucasian. | PMID:28659158 | Finite cell line | Male | CLO:CLO_0023564, Coriell:GM06144, Wikidata:Q54842194 |
CVCL_X456 | 2026-09-19 05:28:05 | 1 | |||||
|
GM06097 Resource Report Resource Website 1+ mentions |
Coriell Cat# GM06097, RRID:CVCL_5U20 | Homo sapiens (Human) | Miller-Dieker syndrome | Population: Caucasian. |
PMID:23665875 PMID:24413397 |
Finite cell line | Female | GM06097A, MDS2 Fib | Coriell | GM06097 | CLO:CLO_0023619, Coriell:GM06097, Wikidata:Q54842162 |
CVCL_5U20 | 2026-09-19 05:28:04 | 1 | ||
|
GM06902 Resource Report Resource Website 1+ mentions |
RRID:CVCL_Y703 | Homo sapiens (Human) | Ornithine carbamoyltransferase deficiency disease | Population: Caucasian. | Finite cell line | Male | GM6902 | CLO:CLO_0036484, Coriell:GM06902, Wikidata:Q54842378 |
CVCL_Y703 | 2026-09-19 05:28:13 | 1 | |||||
|
GM07357 Resource Report Resource Website 1+ mentions |
RRID:CVCL_9595 | Homo sapiens (Human) | Population: Caucasian; Utah residents with ancestry from Northern and Western Europe., Part of: International Genome Sample Resource (1000 genomes project) cell lines., Part of: CEPH/Utah pedigree cell line collection. |
PMID:15514893 PMID:17122850 PMID:19043577 PMID:19797678 PMID:20398888 PMID:20856902 PMID:21397061 PMID:23676674 PMID:24037378 PMID:24924344 PMID:26621101 PMID:27617755 PMID:29116076 PMID:31048460 |
Transformed cell line | Male | CLO:CLO_0016947, EFO:EFO_0001116, ArrayExpress:E-GEUV-1, ArrayExpress:E-GEUV-2, ArrayExpress:E-GEUV-3, ArrayExpress:E-MTAB-3656, ArrayExpress:E-MTAB-3657, ArrayExpress:E-MTAB-5835, Coriell:GM07357, GEO:GSM25426, GEO:GSM25427, GEO:GSM30031, GEO:GSM112493, GEO:GSM112773, GEO:GSM188743, GEO:GSM273289, GEO:GSM273290, GEO:GSM291601, GEO:GSM291602, GEO:GSM314858, GEO:GSM314859, GEO:GSM420582, GEO:GSM420583, GEO:GSM486753, GEO:GSM486754, GEO:GSM648836, GEO:GSM649850, GEO:GSM659955, GEO:GSM660158, GEO:GSM660365, GEO:GSM905829, GEO:GSM905924, GEO:GSM906019, GEO:GSM1719750, IGSR:NA07357, Wikidata:Q54842688 |
CVCL_9595 | 2026-09-19 05:28:22 | 1 | ||||||
|
GM07371 Resource Report Resource Website 1+ mentions |
RRID:CVCL_W727 | Homo sapiens (Human) | Peroxisome biogenesis disorder 7A | Population: Caucasian. | PMID:12851857 | Finite cell line | Female | CLO:CLO_0016943, Coriell:GM07371, Wikidata:Q54842698 |
CVCL_W727 | 2026-09-19 05:28:22 | 1 | |||||
|
GM07522 Resource Report Resource Website 1+ mentions |
RRID:CVCL_F162 | Homo sapiens (Human) | Population: Caucasian. |
PMID:29125828 PMID:32291635 PMID:35850241 |
Finite cell line | Female | C7522 | CLO:CLO_0016443, Coriell:GM07522, GEO:GSM2794413, Wikidata:Q54842822 |
CVCL_F162 | 2026-09-19 05:28:25 | 1 | |||||
|
GM07492 Resource Report Resource Website 1+ mentions Possibly Discontinued |
RRID:CVCL_7467 | Homo sapiens (Human) | Population: Caucasian. |
PMID:29125828 PMID:30567591 PMID:32291635 PMID:35850241 |
Finite cell line | Male | C7492 | CLO:CLO_0016480, Coriell:GM07492, GEO:GSM2794412, GEO:GSM3124644, Wikidata:Q54842796 |
CVCL_7467 | 2026-09-19 05:28:24 | 3 | |||||
|
GM07492 Resource Report Resource Website 1+ mentions Possibly Discontinued |
Coriell Cat# GM07492, RRID:CVCL_7467 | Homo sapiens (Human) | Population: Caucasian. |
PMID:29125828 PMID:30567591 PMID:32291635 PMID:35850241 |
Finite cell line | Male | C7492 | Coriell | GM07492 | CLO:CLO_0016480, Coriell:GM07492, GEO:GSM2794412, GEO:GSM3124644, Wikidata:Q54842796 |
CVCL_7467 | 2026-09-19 05:28:24 | 3 | |||
|
GM07545 Resource Report Resource Website 1+ mentions |
RRID:CVCL_F165 | Homo sapiens (Human) | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0016386, Coriell:GM07545, Wikidata:Q54842848 |
CVCL_F165 | 2026-09-19 05:28:25 | 2 | |||||||
|
GM03468 Resource Report Resource Website 1+ mentions |
RRID:CVCL_7389 | Homo sapiens (Human) | Population: Caucasian. |
PMID:6458814 PMID:6621576 PMID:6726265 |
Finite cell line | Male | GM3468, GM 3468, GM03468A, GM3468A | CLO:CLO_0017027, BioSample:SAMN00808416, Coriell:GM03468, Wikidata:Q54838083 |
CVCL_7389 | 2026-09-19 05:27:32 | 1 | |||||
|
GM03468 Resource Report Resource Website 1+ mentions |
Coriell Cat# GM03468, RRID:CVCL_7389 | Homo sapiens (Human) | Population: Caucasian. |
PMID:6458814 PMID:6621576 PMID:6726265 |
Finite cell line | Male | GM3468, GM 3468, GM03468A, GM3468A | Coriell | GM03468 | CLO:CLO_0017027, BioSample:SAMN00808416, Coriell:GM03468, Wikidata:Q54838083 |
CVCL_7389 | 2026-09-19 05:27:32 | 1 | |||
|
GM03538 Resource Report Resource Website 1+ mentions |
RRID:CVCL_X290 | Homo sapiens (Human) | Trisomy 18 | Karyotypic information: 47,XX,+18 (Coriell=GM03538)., Population: Caucasian. | PMID:6661932 | Finite cell line | Female | GM 3538 | CLO:CLO_0017309, BioSample:SAMN00808442, Coriell:GM03538, Wikidata:Q54838120 |
CVCL_X290 | 2026-09-19 05:27:32 | 1 | ||||
|
GM03543 Resource Report Resource Website 1+ mentions |
RRID:CVCL_X291 | Homo sapiens (Human) | Turner syndrome | PMID:6661932 | Transformed cell line | Female | GM 3543 | CLO:CLO_0017306, BioSample:SAMN00808444, Coriell:GM03543, Wikidata:Q54838122 |
CVCL_X291 | 2026-09-19 05:27:32 | 1 |
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