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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 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM16586 Resource Report Resource Website |
RRID:CVCL_0G75 | Homo sapiens (Human) | Holoprosencephaly |
PMID:7485158 PMID:23665875 |
Transformed cell line | Male | JL218 | CLO:CLO_0017390, Coriell:GM16586, Wikidata:Q54848646 |
CVCL_0G75 | Cellosaurus | 2026-10-17 06:17:37 | 0 | |||||
|
GM16595 Resource Report Resource Website |
Coriell Cat# GM16595, RRID:CVCL_5Q73 | Homo sapiens (Human) | Cri du chat syndrome | Population: Cuban. | PMID:23665875 | Transformed cell line | Female | JL163 | Coriell | GM16595 | CLO:CLO_0017403, Coriell:GM16595, Wikidata:Q54848670 |
CVCL_5Q73 | Cellosaurus | 2026-10-17 06:17:37 | 0 | ||
|
GM16593 Resource Report Resource Website |
Coriell Cat# GM16593, RRID:CVCL_5Q71 | Homo sapiens (Human) | Cri du chat syndrome | PMID:23665875 | Transformed cell line | Female | JL444 | Coriell | GM16593 | CLO:CLO_0017398, Coriell:GM16593, Wikidata:Q54848668 |
CVCL_5Q71 | Cellosaurus | 2026-10-17 06:17:37 | 0 | |||
|
GM16582 Resource Report Resource Website |
Coriell Cat# GM16582, RRID:CVCL_0G73 | Homo sapiens (Human) | Holoprosencephaly | PMID:23665875 | Transformed cell line | Male | JL376 | Coriell | GM16582 | CLO:CLO_0017552, Coriell:GM16582, Wikidata:Q54848642 |
CVCL_0G73 | Cellosaurus | 2026-10-17 06:17:37 | 0 | |||
|
GM16810 Resource Report Resource Website |
RRID:CVCL_5Q81 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | Coriell:GM16810, Wikidata:Q54848757 |
CVCL_5Q81 | Cellosaurus | 2026-10-17 06:17:39 | 0 | |||||||
|
GM16736 Resource Report Resource Website |
RRID:CVCL_5Q77 | Homo sapiens (Human) | Deafness |
PMID:23661601 PMID:23665875 |
Transformed cell line | Male | Coriell:GM16736, Wikidata:Q54848720 |
CVCL_5Q77 | Cellosaurus | 2026-10-17 06:17:38 | 0 | ||||||
|
GM16808 Resource Report Resource Website |
Coriell Cat# GM16808, RRID:CVCL_5Q79 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | Coriell | GM16808 | Coriell:GM16808, Wikidata:Q54848755 |
CVCL_5Q79 | Cellosaurus | 2026-10-17 06:17:39 | 0 | |||||
|
GM16994 Resource Report Resource Website |
RRID:CVCL_2N34 | Homo sapiens (Human) | Autism spectrum disorder | PMID:23665875 | Transformed cell line | Male | Coriell:GM16994, Wikidata:Q54848827 |
CVCL_2N34 | Cellosaurus | 2026-10-17 06:17:40 | 0 | ||||||
|
GM12959 Resource Report Resource Website |
RRID:CVCL_5P71 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | CLO:CLO_0022918, Coriell:GM12959, Wikidata:Q54846240 |
CVCL_5P71 | Cellosaurus | 2026-10-17 06:16:43 | 0 | |||||||
|
GM13164 Resource Report Resource Website |
Coriell Cat# GM13164, RRID:CVCL_4W21 | Homo sapiens (Human) | Rubinstein-Taybi syndrome | Population: African American. | PMID:23665875 | Transformed cell line | Female | Coriell | GM13164 | CLO:CLO_0013645, BioSample:SAMN00802155, Coriell:GM13164, Wikidata:Q54846354 |
CVCL_4W21 | Cellosaurus | 2026-10-17 06:16:45 | 0 | |||
|
GM13166 Resource Report Resource Website |
Coriell Cat# GM13166, RRID:CVCL_2Q71 | Homo sapiens (Human) | Turner syndrome | PMID:23665875 | Transformed cell line | Female | Coriell | GM13166 | CLO:CLO_0013643, Coriell:GM13166, Wikidata:Q54846355 |
CVCL_2Q71 | Cellosaurus | 2026-10-17 06:16:45 | 0 | ||||
|
GM13164 Resource Report Resource Website |
RRID:CVCL_4W21 | Homo sapiens (Human) | Rubinstein-Taybi syndrome | Population: African American. | PMID:23665875 | Transformed cell line | Female | CLO:CLO_0013645, BioSample:SAMN00802155, Coriell:GM13164, Wikidata:Q54846354 |
CVCL_4W21 | Cellosaurus | 2026-10-17 06:16:45 | 0 | |||||
|
GM13277 Resource Report Resource Website |
RRID:CVCL_5P73 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | CLO:CLO_0013290, BioSample:SAMN00802246, Coriell:GM13277, Wikidata:Q54846416 |
CVCL_5P73 | Cellosaurus | 2026-10-17 06:16:47 | 0 | |||||||
|
GM13284 Resource Report Resource Website |
Coriell Cat# GM13284, RRID:CVCL_2U25 | Homo sapiens (Human) | Population: Caucasian. | PMID:23665875 | Finite cell line | Male | Coriell | GM13284 | CLO:CLO_0013286, BioSample:SAMN00802254, Coriell:GM13284, Wikidata:Q54846420 |
CVCL_2U25 | Cellosaurus | 2026-10-17 06:16:47 | 0 | ||||
|
GM13330 Resource Report Resource Website |
Coriell Cat# GM13330, RRID:CVCL_2U26 | Homo sapiens (Human) | Population: Caucasian. |
PMID:11687795 PMID:23665875 |
Finite cell line | Male | Coriell | GM13330 | CLO:CLO_0013247, BioSample:SAMN00802309, Coriell:GM13330, GEO:GSM809, Wikidata:Q54846466 |
CVCL_2U26 | Cellosaurus | 2026-10-17 06:16:48 | 0 | ||||
|
GM13451 Resource Report Resource Website |
RRID:CVCL_5P80 | Homo sapiens (Human) | Holoprosencephaly | PMID:23665875 | Finite cell line | Male | Coriell:GM13451, Wikidata:Q54846537 |
CVCL_5P80 | Cellosaurus | 2026-10-17 06:16:49 | 0 | ||||||
|
GM13321 Resource Report Resource Website |
Coriell Cat# GM13321, RRID:CVCL_N207 | Homo sapiens (Human) | Population: African American., Part of: Human variation panel. |
PMID:16260726 PMID:23665875 |
Transformed cell line | Male | GM17174 | Coriell | GM13321 | CLO:CLO_0013224, CLO:CLO_0014034, BioSample:SAMN00802297, Coriell:GM13321, Coriell:GM17174, GEO:GSM569746, GEO:GSM596238, GEO:GSM597033, GEO:GSM924684, Wikidata:Q54846458 |
CVCL_N207 | Cellosaurus | 2026-10-17 06:16:48 | 0 | |||
|
GM13451 Resource Report Resource Website |
Coriell Cat# GM13451, RRID:CVCL_5P80 | Homo sapiens (Human) | Holoprosencephaly | PMID:23665875 | Finite cell line | Male | Coriell | GM13451 | Coriell:GM13451, Wikidata:Q54846537 |
CVCL_5P80 | Cellosaurus | 2026-10-17 06:16:49 | 0 | ||||
|
GM13323 Resource Report Resource Website |
Coriell Cat# GM13323, RRID:CVCL_2N04 | Homo sapiens (Human) | Turner syndrome | Donor information: Established from monozygotic twin of GM13324 (Cellosaurus=CVCL_2N05). | PMID:23665875 | Transformed cell line | Female | Coriell | GM13323 | CLO:CLO_0013275, Coriell:GM13323, Wikidata:Q54846460 |
CVCL_2N04 | Cellosaurus | 2026-10-17 06:16:48 | 0 | |||
|
GM13324 Resource Report Resource Website |
RRID:CVCL_2N05 | Homo sapiens (Human) | Turner syndrome | Donor information: Established from monozygotic twin of GM13323 (Cellosaurus=CVCL_2N04). | PMID:23665875 | Transformed cell line | Female | CLO:CLO_0013274, Coriell:GM13324, Wikidata:Q54846461 |
CVCL_2N05 | Cellosaurus | 2026-10-17 06:16:48 | 0 |
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