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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM13204 Resource Report Resource Website |
RRID:CVCL_U401 | Homo sapiens (Human) | Tay-Sachs disease | Finite cell line | Female | CLO:CLO_0013206, Coriell:GM13204, Wikidata:Q54846380 |
CVCL_U401 | 2026-08-01 05:07:00 | 0 | |||||||
|
GM13118 Resource Report Resource Website |
Coriell Cat# GM13118, RRID:CVCL_9Y21 | Homo sapiens (Human) | Population: Caucasian; Amish., Part of: CEPH/Amish pedigree cell line collection. | Transformed cell line | Female | Coriell | GM13118 | CLO:CLO_0013925, BioSample:SAMN00802111, Coriell:GM13118, GEO:GSM617128, Wikidata:Q54846325 |
CVCL_9Y21 | 2026-08-01 05:07:00 | 0 | |||||
|
GM13147 Resource Report Resource Website |
Coriell Cat# GM13147, RRID:CVCL_DB84 | Homo sapiens (Human) | Population: Caucasian; Amish. | Transformed cell line | Female | Coriell | GM13147 | CLO:CLO_0013671, BioSample:SAMN00802147, Coriell:GM13147, Wikidata:Q54846350 |
CVCL_DB84 | 2026-08-01 05:07:01 | 0 | |||||
|
GM13239 Resource Report Resource Website |
RRID:CVCL_9Y33 | Homo sapiens (Human) | Sly syndrome | Population: Mexican. | Finite cell line | Female | CLO:CLO_0013192, BioSample:SAMN00802198, Coriell:GM13239, Wikidata:Q54846385 |
CVCL_9Y33 | 2026-08-01 05:07:01 | 0 | ||||||
|
GM13287 Resource Report Resource Website |
Coriell Cat# GM13287, RRID:CVCL_4Z71 | Homo sapiens (Human) | Trichothiodystrophy | Population: Caucasian. | Finite cell line | Male | Coriell | GM13287 | CLO:CLO_0013352, BioSample:SAMN00802258, Coriell:GM13287, Wikidata:Q54846422 |
CVCL_4Z71 | 2026-08-01 05:07:02 | 0 | ||||
|
GM13284 Resource Report Resource Website |
RRID:CVCL_2U25 | Homo sapiens (Human) | Population: Caucasian. | PMID:23665875 | Finite cell line | Male | CLO:CLO_0013286, BioSample:SAMN00802254, Coriell:GM13284, Wikidata:Q54846420 |
CVCL_2U25 | 2026-08-01 05:07:07 | 0 | ||||||
|
GM13298 Resource Report Resource Website |
RRID:CVCL_9R32 | Homo sapiens (Human) | Neonatal adrenoleukodystrophy | Population: Caucasian. | Finite cell line | Male | CLO:CLO_0013327, BioSample:SAMN00802271, Coriell:GM13298, Wikidata:Q54846430 |
CVCL_9R32 | 2026-08-01 05:07:02 | 0 | ||||||
|
GM13247 Resource Report Resource Website |
RRID:CVCL_V395 | Homo sapiens (Human) | Glycogen storage disease type Ia | Transformed cell line | Male | CLO:CLO_0013186, BioSample:SAMN00802206, Coriell:GM13247, Wikidata:Q54846393 |
CVCL_V395 | 2026-08-01 05:07:02 | 0 | |||||||
|
GM13255 Resource Report Resource Website |
RRID:CVCL_V143 | Homo sapiens (Human) | Von Hippel-Lindau syndrome | Transformed cell line | Male | CLO:CLO_0013088, BioSample:SAMN00802216, Coriell:GM13255, Wikidata:Q54846400 |
CVCL_V143 | 2026-08-01 05:07:03 | 0 | |||||||
|
GM13302 Resource Report Resource Website |
RRID:CVCL_1S67 | Cricetulus griseus (Chinese hamster) | Group: Human/rodent somatic cell hybrid. | PMID:8404043 | Hybrid cell line | UMHG-17/1A | CLO:CLO_0013321, Coriell:GM13302, Wikidata:Q54846432 |
cvcl_k265 | CVCL_1S67 | 2026-08-01 05:07:04 | 0 | |||||
|
GM13275 Resource Report Resource Website |
RRID:CVCL_4F71 | Homo sapiens (Human) | Medium-chain acyl-CoA dehydrogenase deficiency | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0013288, BioSample:SAMN00802242, Coriell:GM13275, Wikidata:Q54846414 |
CVCL_4F71 | 2026-08-01 05:07:03 | 0 | ||||||
|
GM13286 Resource Report Resource Website |
RRID:CVCL_4Z70 | Homo sapiens (Human) | Trichothiodystrophy | Population: Caucasian. | Transformed cell line | Male | GM13286A | CLO:CLO_0013300, BioSample:SAMN00802256, Coriell:GM13286, Wikidata:Q54846421 |
CVCL_4Z70 | 2026-08-01 05:07:02 | 0 | |||||
|
GM13242 Resource Report Resource Website |
RRID:CVCL_GZ46 | Homo sapiens (Human) | Congenital bilateral aplasia of the vas deferens | Transformed cell line | Male | CLO:CLO_0013189, BioSample:SAMN00802202, Coriell:GM13242, Wikidata:Q54846387 |
CVCL_GZ46 | 2026-08-01 05:07:06 | 0 | |||||||
|
GM13311 Resource Report Resource Website |
RRID:CVCL_4F07 | Homo sapiens (Human) | Ellis-Van Creveld syndrome | Population: Caucasian; Amish. | Transformed cell line | Female | CLO:CLO_0013215, BioSample:SAMN00802287, Coriell:GM13311, Wikidata:Q54846451 |
CVCL_4F07 | 2026-08-01 05:07:02 | 0 | ||||||
|
GM13243 Resource Report Resource Website |
Coriell Cat# GM13243, RRID:CVCL_V394 | Homo sapiens (Human) | Glycogen storage disease type Ia | Transformed cell line | Female | Coriell | GM13243 | CLO:CLO_0013187, BioSample:SAMN00802204, Coriell:GM13243, Wikidata:Q54846392 |
CVCL_V394 | 2026-08-01 05:07:06 | 0 | |||||
|
GM13206 Resource Report Resource Website |
Coriell Cat# GM13206, RRID:CVCL_IJ39 | Homo sapiens (Human) | Galactosialidosis | Finite cell line | Male | Coriell | GM13206 | CLO:CLO_0013198, Coriell:GM13206, Wikidata:Q54846382 |
CVCL_IJ39 | 2026-08-01 05:07:00 | 0 | |||||
|
GM13272 Resource Report Resource Website |
Coriell Cat# GM13272, RRID:CVCL_4F69 | Homo sapiens (Human) | Zellweger syndrome | Population: Caucasian. | Finite cell line | Female | Coriell | GM13272 | CLO:CLO_0013313, BioSample:SAMN00802238, Coriell:GM13272, Wikidata:Q54846412 |
CVCL_4F69 | 2026-08-01 05:07:03 | 0 | ||||
|
GM13238 Resource Report Resource Website |
Coriell Cat# GM13238, RRID:CVCL_2U24 | Homo sapiens (Human) | Karyotypic information: 46,XX,t(1;13)(1pter->1q25::13q22->13qter;13pter->13q22::1q25->1qter) (Coriell=GM13238). | Finite cell line | Female | Coriell | GM13238 | CLO:CLO_0013196, Coriell:GM13238, Wikidata:Q54846383 |
CVCL_2U24 | 2026-08-01 05:07:02 | 0 | |||||
|
GM13206 Resource Report Resource Website |
RRID:CVCL_IJ39 | Homo sapiens (Human) | Galactosialidosis | Finite cell line | Male | CLO:CLO_0013198, Coriell:GM13206, Wikidata:Q54846382 |
CVCL_IJ39 | 2026-08-01 05:07:02 | 0 | |||||||
|
GM13256 Resource Report Resource Website |
Coriell Cat# GM13256, RRID:CVCL_V144 | Homo sapiens (Human) | Von Hippel-Lindau syndrome | Transformed cell line | Male | Coriell | GM13256 | CLO:CLO_0013063, BioSample:SAMN00802218, Coriell:GM13256, Wikidata:Q54846402 |
CVCL_V144 | 2026-08-01 05:07:03 | 0 |
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