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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 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM50188 Resource Report Resource Website |
Coriell Cat# GM50188, RRID:CVCL_5T56 | Homo sapiens (Human) | Cri du chat syndrome | Population: Lebanese. | PMID:23665875 | Transformed cell line | Female | Coriell | GM50188 | Coriell:GM50188, Wikidata:Q54854253 |
CVCL_5T56 | Cellosaurus | 2026-10-17 06:20:08 | 0 | |||
|
GM50275 Resource Report Resource Website |
RRID:CVCL_5T61 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | Coriell:GM50275, Wikidata:Q54854262 |
CVCL_5T61 | Cellosaurus | 2026-10-17 06:20:08 | 0 | |||||||
|
GM50178 Resource Report Resource Website |
Coriell Cat# GM50178, RRID:CVCL_0G67 | Homo sapiens (Human) | Cri du chat syndrome | PMID:23665875 | Transformed cell line | Female | JL378 | Coriell | GM50178 | CLO:CLO_0014986, Coriell:GM50178, Wikidata:Q54854249 |
CVCL_0G67 | Cellosaurus | 2026-10-17 06:20:08 | 0 | |||
|
GM50322 Resource Report Resource Website |
RRID:CVCL_1U17 | Homo sapiens (Human) | Deletion 18p syndrome |
PMID:1577474 PMID:23665875 |
Transformed cell line | Female | JL91 | CLO:CLO_0012521, Coriell:GM50322, Wikidata:Q54854268 |
CVCL_1U17 | Cellosaurus | 2026-10-17 06:20:08 | 0 | |||||
|
GM50323 Resource Report Resource Website |
Coriell Cat# GM50323, RRID:CVCL_1U18 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | JL92 | Coriell | GM50323 | CLO:CLO_0012520, Coriell:GM50323, Wikidata:Q54854269 |
CVCL_1U18 | Cellosaurus | 2026-10-17 06:20:09 | 0 | ||||
|
GM15913 Resource Report Resource Website |
Coriell Cat# GM15913, RRID:CVCL_5Q61 | Homo sapiens (Human) | Waardenburg syndrome type 4 | Population: African American. | PMID:23665875 | Transformed cell line | Female | Coriell | GM15913 | Coriell:GM15913, Wikidata:Q54848276 |
CVCL_5Q61 | Cellosaurus | 2026-10-17 06:17:29 | 0 | |||
|
GM16098 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM16098, RRID:CVCL_5Q62 | Homo sapiens (Human) | Nijmegen breakage syndrome | PMID:23665875 | Finite cell line | Female | Coriell | GM16098 | Coriell:GM16098, Wikidata:Q54848320 |
CVCL_5Q62 | Cellosaurus | 2026-10-17 06:17:30 | 0 | ||||
|
GM16158 Resource Report Resource Website |
RRID:CVCL_5Q64 | Homo sapiens (Human) | Orofacial cleft 1 | PMID:23665875 | Transformed cell line | Male | Coriell:GM16158, Wikidata:Q54848342 |
CVCL_5Q64 | Cellosaurus | 2026-10-17 06:17:31 | 0 | ||||||
|
GM16158 Resource Report Resource Website |
Coriell Cat# GM16158, RRID:CVCL_5Q64 | Homo sapiens (Human) | Orofacial cleft 1 | PMID:23665875 | Transformed cell line | Male | Coriell | GM16158 | Coriell:GM16158, Wikidata:Q54848342 |
CVCL_5Q64 | Cellosaurus | 2026-10-17 06:17:31 | 0 | ||||
|
GM16362 Resource Report Resource Website |
Coriell Cat# GM16362, RRID:CVCL_5Q66 | Homo sapiens (Human) | Donor information: Established from monozygotic twin of GM16363 (Cellosaurus=CVCL_5Q67). | PMID:23665875 | Transformed cell line | Male | Coriell | GM16362 | Coriell:GM16362, Wikidata:Q54848471 |
CVCL_5Q66 | Cellosaurus | 2026-10-17 06:17:34 | 0 | ||||
|
GM16457 Resource Report Resource Website |
Coriell Cat# GM16457, RRID:CVCL_5L24 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Female | JL404 | Coriell | GM16457 | CLO:CLO_0017820, Coriell:GM16457, Wikidata:Q54848577 |
CVCL_5L24 | Cellosaurus | 2026-10-17 06:17:36 | 0 | |||
|
GM16451 Resource Report Resource Website |
Coriell Cat# GM16451, RRID:CVCL_0H49 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Male | JL359 | Coriell | GM16451 | CLO:CLO_0017806, Coriell:GM16451, Wikidata:Q54848571 |
CVCL_0H49 | Cellosaurus | 2026-10-17 06:17:36 | 0 | |||
|
GM16453 Resource Report Resource Website |
RRID:CVCL_0H50 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Male | JL360 | CLO:CLO_0017804, Coriell:GM16453, Wikidata:Q54848573 |
CVCL_0H50 | Cellosaurus | 2026-10-17 06:17:36 | 0 | |||||
|
GM16447 Resource Report Resource Website |
RRID:CVCL_5L23 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Male | JL288 | CLO:CLO_0017803, Coriell:GM16447, Wikidata:Q54848567 |
CVCL_5L23 | Cellosaurus | 2026-10-17 06:17:35 | 0 | |||||
|
GM16459 Resource Report Resource Website |
Coriell Cat# GM16459, RRID:CVCL_0H52 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Male | JL421 | Coriell | GM16459 | CLO:CLO_0017821, Coriell:GM16459, Wikidata:Q54848578 |
CVCL_0H52 | Cellosaurus | 2026-10-17 06:17:36 | 0 | |||
|
GM16455 Resource Report Resource Website |
Coriell Cat# GM16455, RRID:CVCL_0H51 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Female | JL401 | Coriell | GM16455 | CLO:CLO_0017811, Coriell:GM16455, Wikidata:Q54848575 |
CVCL_0H51 | Cellosaurus | 2026-10-17 06:17:36 | 0 | |||
|
GM16438 Resource Report Resource Website |
Coriell Cat# GM16438, RRID:CVCL_0H47 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | JL480 | Coriell | GM16438 | CLO:CLO_0017782, Coriell:GM16438, Wikidata:Q54848560 |
CVCL_0H47 | Cellosaurus | 2026-10-17 06:17:35 | 0 | ||||
|
GM16459 Resource Report Resource Website |
RRID:CVCL_0H52 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Male | JL421 | CLO:CLO_0017821, Coriell:GM16459, Wikidata:Q54848578 |
CVCL_0H52 | Cellosaurus | 2026-10-17 06:17:36 | 0 | |||||
|
GM16584 Resource Report Resource Website |
RRID:CVCL_0G74 | Homo sapiens (Human) | Holoprosencephaly | PMID:23665875 | Transformed cell line | Female | JL257 | CLO:CLO_0017548, Coriell:GM16584, Wikidata:Q54848644 |
CVCL_0G74 | Cellosaurus | 2026-10-17 06:17:37 | 0 | |||||
|
GM16595 Resource Report Resource Website |
RRID:CVCL_5Q73 | Homo sapiens (Human) | Cri du chat syndrome | Population: Cuban. | PMID:23665875 | Transformed cell line | Female | JL163 | CLO:CLO_0017403, Coriell:GM16595, Wikidata:Q54848670 |
CVCL_5Q73 | Cellosaurus | 2026-10-17 06:17:37 | 0 |
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