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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM19924 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_1A88 | Homo sapiens (Human) | Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines. | Transformed cell line | Female | Coriell:GM19924, IGSR:NA19924, Wikidata:Q54850757 |
CVCL_1A88 | 2026-07-25 04:36:47 | 0 | |||||||
|
GM20005 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_F637 | Homo sapiens (Human) | Glycogen storage disease type II | Population: African American. | Transformed cell line | Male | CLO:CLO_0028365, BioSample:SAMN00805638, Coriell:GM20005, Wikidata:Q54850777 |
cvcl_f601 | CVCL_F637 | 2026-07-25 04:36:47 | 0 | |||||
|
GM20312 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM20312, RRID:CVCL_1B05 | Homo sapiens (Human) | Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines. | Transformed cell line | Female | Coriell | GM20312 | Coriell:GM20312, IGSR:NA20312, Wikidata:Q54850925 |
CVCL_1B05 | 2026-07-25 04:36:50 | 0 | |||||
|
GM20285 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM20285, RRID:CVCL_1A96 | Homo sapiens (Human) | Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines. | Transformed cell line | Male | Coriell | GM20285 | Coriell:GM20285, IGSR:NA20285, Wikidata:Q54850891 |
CVCL_1A96 | 2026-07-25 04:36:50 | 0 | |||||
|
GM20466 Resource Report Resource Website Discontinued |
RRID:CVCL_7660 | Homo sapiens (Human) | Roberts-SC phocomelia syndrome | PMID:16380922 | Transformed cell line | Female | AG04344, AG4344 | CLO:CLO_0029512, BioSample:SAMN00805846, Coriell:AG04344, Coriell:GM20466, Wikidata:Q54851039 |
CVCL_7660 | 2026-07-25 04:36:53 | 0 | |||||
|
GM20413 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM20413, RRID:CVCL_1B26 | Homo sapiens (Human) | Population: African ancestry in Southwest USA (ASW)., Part of: International Genome Sample Resource (1000 genomes project) cell lines. | Transformed cell line | Male | Coriell | GM20413 | Coriell:GM20413, IGSR:NA20413, Wikidata:Q54851015 |
CVCL_1B26 | 2026-07-25 04:36:52 | 0 | |||||
|
GM22931 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_5S34 | Homo sapiens (Human) | 1p36 deletion syndrome | PMID:23665875 | Transformed cell line | Male | Coriell:GM22931, Wikidata:Q54852836 |
CVCL_5S34 | 2026-07-25 04:37:31 | 0 | ||||||
|
GM23340 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_F184 | Homo sapiens (Human) | Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection. | Induced pluripotent stem cell | Male | GM23340*A | Coriell:GM23340, SKIP:SKIP000179, SKIP:SKIP004356, Wikidata:Q54853012 |
cvcl_f185 | CVCL_F184 | 2026-07-25 04:37:34 | 0 | |||||
|
GM23280 Resource Report Resource Website 1+ mentions Possibly Discontinued |
Coriell Cat# GM23280, RRID:CVCL_F179 | Homo sapiens (Human) | Caution: May be identical to one of the many iPSC cell lines produced from HDF1388 by the Center for iPS Cell Research and Application (CiRA)., Population: Caucasian. | PMID:27264186 | Induced pluripotent stem cell | Female | GM23280A, GM23280*A | Coriell | GM23280 | Coriell:GM23280, SKIP:SKIP000387, SKIP:SKIP004353, Wikidata:Q54852964 |
cvcl_dp59 | CVCL_F179 | 2026-07-25 04:37:33 | 1 | ||
|
GM23394 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_F166 | Homo sapiens (Human) | Population: African American. | Induced pluripotent stem cell | Male | GM23394*B | Coriell:GM23394, SKIP:SKIP000180, SKIP:SKIP004359, Wikidata:Q54853048 |
cvcl_7477 | CVCL_F166 | 2026-07-25 04:37:35 | 0 | |||||
|
GM23394 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM23394, RRID:CVCL_F166 | Homo sapiens (Human) | Population: African American. | Induced pluripotent stem cell | Male | GM23394*B | Coriell | GM23394 | Coriell:GM23394, SKIP:SKIP000180, SKIP:SKIP004359, Wikidata:Q54853048 |
cvcl_7477 | CVCL_F166 | 2026-07-25 04:37:35 | 0 | |||
|
GM23778 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_4T52 | Homo sapiens (Human) | Ullrich congenital muscular dystrophy | Finite cell line | Male | Coriell:GM23778, Wikidata:Q54853303 |
CVCL_4T52 | 2026-07-25 04:37:40 | 0 | |||||||
|
GM23906 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_5T33 | Homo sapiens (Human) | Hyperglycerolemia | PMID:23665875 | Transformed cell line | Male | Coriell:GM23906, Wikidata:Q54853432 |
CVCL_5T33 | 2026-07-25 04:37:42 | 0 | ||||||
|
GM24224 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_4T59 | Homo sapiens (Human) | Ullrich congenital muscular dystrophy | Finite cell line | Male | Coriell:GM24224, Wikidata:Q54853641 |
CVCL_4T59 | 2026-07-25 04:37:47 | 0 | |||||||
|
GM15789 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_0Q31 | Homo sapiens (Human) | Nijmegen breakage syndrome | Population: Caucasian; Czechoslovakian. | Finite cell line | Male | Coriell:GM15789, Wikidata:Q54848201 |
CVCL_0Q31 | 2026-07-25 04:35:52 | 0 | ||||||
|
GM15776 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM15776, RRID:CVCL_1S97 | Cricetulus griseus (Chinese hamster) | Group: Human/rodent somatic cell hybrid. | Hybrid cell line | Coriell | GM15776 | Coriell:GM15776, Wikidata:Q54848196 |
cvcl_1q37 | CVCL_1S97 | 2026-07-25 04:35:52 | 0 | |||||
|
GM16098 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_5Q62 | Homo sapiens (Human) | Nijmegen breakage syndrome | PMID:23665875 | Finite cell line | Female | Coriell:GM16098, Wikidata:Q54848320 |
CVCL_5Q62 | 2026-07-25 04:35:54 | 0 | ||||||
|
GM16101 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A5WN | Homo sapiens (Human) | PMID:28161093 | Transformed cell line | Female | Coriell:GM16101, Wikidata:Q107115128 |
CVCL_A5WN | 2026-07-25 04:35:54 | 0 | |||||||
|
GM16292 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A5WI | Homo sapiens (Human) | PMID:28161093 | Transformed cell line | Female | Coriell:GM16292, Wikidata:Q107115152 |
CVCL_A5WI | 2026-07-25 04:35:56 | 0 | |||||||
|
GM16289 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A5WF | Homo sapiens (Human) | PMID:28161093 | Transformed cell line | Female | Coriell:GM16289, Wikidata:Q107115145 |
CVCL_A5WF | 2026-07-25 04:35:56 | 0 |
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Data set from Kravitz, Owen and Kretizer's 2012 paper "Optogenetic identification of striatal projection neuron subtypes during in vivo recordings."
