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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM50152 Resource Report Resource Website |
RRID:CVCL_5L26 | Homo sapiens (Human) | Deletion 18p syndrome | PMID:23665875 | Transformed cell line | Female | JL280 | CLO:CLO_0014709, Coriell:GM50152, Wikidata:Q54854225 |
CVCL_5L26 | 2026-02-07 08:11:38 | 0 | |||||
|
GM50172 Resource Report Resource Website |
Coriell Cat# GM50172, RRID:CVCL_5L32 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Female | JL351 | Coriell | GM50172 | CLO:CLO_0015028, Coriell:GM50172, Wikidata:Q54854244 |
CVCL_5L32 | 2026-02-07 08:11:33 | 0 | |||
|
GM50148 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_5T51 | Homo sapiens (Human) | Deletion 18p syndrome | PMID:23665875 | Transformed cell line | Female | Coriell:GM50148, Wikidata:Q54854222 |
CVCL_5T51 | 2026-02-07 08:11:38 | 0 | ||||||
|
GM50114 Resource Report Resource Website |
Coriell Cat# GM50114, RRID:CVCL_5T46 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | Coriell | GM50114 | Coriell:GM50114, Wikidata:Q54854202 |
CVCL_5T46 | 2026-02-07 08:11:37 | 0 | |||||
|
GM50124 Resource Report Resource Website |
RRID:CVCL_1U16 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Male | JL208 | CLO:CLO_0014753, Coriell:GM50124, Wikidata:Q54854209 |
CVCL_1U16 | 2026-02-07 08:11:44 | 0 | |||||
|
GM50165 Resource Report Resource Website |
Coriell Cat# GM50165, RRID:CVCL_5L30 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Male | JL330 | Coriell | GM50165 | CLO:CLO_0015015, Coriell:GM50165, Wikidata:Q54854238 |
CVCL_5L30 | 2026-02-07 08:11:33 | 0 | |||
|
GM50160 Resource Report Resource Website |
Coriell Cat# GM50160, RRID:CVCL_5L28 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Female | JL305 | Coriell | GM50160 | CLO:CLO_0014717, Coriell:GM50160, Wikidata:Q54854234 |
CVCL_5L28 | 2026-02-07 08:11:33 | 0 | |||
|
GM50114 Resource Report Resource Website |
RRID:CVCL_5T46 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | Coriell:GM50114, Wikidata:Q54854202 |
CVCL_5T46 | 2026-02-07 08:11:32 | 0 | |||||||
|
GM50172 Resource Report Resource Website |
RRID:CVCL_5L32 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Female | JL351 | CLO:CLO_0015028, Coriell:GM50172, Wikidata:Q54854244 |
CVCL_5L32 | 2026-02-07 08:11:44 | 0 | |||||
|
GM50159 Resource Report Resource Website |
Coriell Cat# GM50159, RRID:CVCL_5T53 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | JL298 | Coriell | GM50159 | CLO:CLO_0014716, Coriell:GM50159, Wikidata:Q54854229 |
CVCL_5T53 | 2026-02-07 08:11:38 | 0 | ||||
|
GM50126 Resource Report Resource Website |
RRID:CVCL_0G80 | Homo sapiens (Human) | Holoprosencephaly |
PMID:7485158 PMID:23665875 |
Transformed cell line | Female | JL219 | CLO:CLO_0014670, Coriell:GM50126, Wikidata:Q54854211 |
CVCL_0G80 | 2026-02-07 08:11:32 | 0 | |||||
|
GM50163 Resource Report Resource Website |
RRID:CVCL_0H56 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Female | JL317 | CLO:CLO_0014722, Coriell:GM50163, Wikidata:Q54854235 |
CVCL_0H56 | 2026-02-07 08:11:38 | 0 | |||||
|
GM50164 Resource Report Resource Website |
RRID:CVCL_5L29 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Female | JL325 | CLO:CLO_0014721, Coriell:GM50164, Wikidata:Q54854236 |
CVCL_5L29 | 2026-02-07 08:11:33 | 0 | |||||
|
GM50142 Resource Report Resource Website |
Coriell Cat# GM50142, RRID:CVCL_5T49 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | JL263 | Coriell | GM50142 | CLO:CLO_0014676, Coriell:GM50142, Wikidata:Q54854217 |
CVCL_5T49 | 2026-02-07 08:11:38 | 0 | ||||
|
GM50125 Resource Report Resource Website |
RRID:CVCL_0F94 | Homo sapiens (Human) | Deletion 18q syndrome |
PMID:8488839 PMID:23665875 |
Transformed cell line | Female | JL209 | CLO:CLO_0014669, Coriell:GM50125, Wikidata:Q54854210 |
CVCL_0F94 | 2026-02-07 08:11:37 | 0 | |||||
|
GM50324 Resource Report Resource Website |
RRID:CVCL_5T64 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | Coriell:GM50324, Wikidata:Q54854270 |
CVCL_5T64 | 2026-02-07 08:11:34 | 0 | |||||||
|
GM50248 Resource Report Resource Website |
RRID:CVCL_5T60 | Homo sapiens (Human) | Cri du chat syndrome | PMID:23665875 | Transformed cell line | Male | Coriell:GM50248, Wikidata:Q54854261 |
CVCL_5T60 | 2026-02-07 08:11:34 | 0 | ||||||
|
GM50284 Resource Report Resource Website |
Coriell Cat# GM50284, RRID:CVCL_5T63 | Homo sapiens (Human) | Cri du chat syndrome | PMID:23665875 | Transformed cell line | Female | Coriell | GM50284 | Coriell:GM50284, Wikidata:Q54854264 |
CVCL_5T63 | 2026-02-07 08:11:40 | 0 | ||||
|
GM50193 Resource Report Resource Website |
RRID:CVCL_5L36 | Homo sapiens (Human) | Deletion 18p syndrome | PMID:23665875 | Transformed cell line | Female | JL451 | CLO:CLO_0014989, Coriell:GM50193, Wikidata:Q54854256 |
CVCL_5L36 | 2026-02-07 08:11:44 | 0 | |||||
|
GM50322 Resource Report Resource Website |
Coriell Cat# GM50322, RRID:CVCL_1U17 | Homo sapiens (Human) | Deletion 18p syndrome |
PMID:1577474 PMID:23665875 |
Transformed cell line | Female | JL91 | Coriell | GM50322 | CLO:CLO_0012521, Coriell:GM50322, Wikidata:Q54854268 |
CVCL_1U17 | 2026-02-07 08:11:34 | 0 |
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