Searching the RRID Resource Information Network
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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GMS-10 Resource Report Resource Website |
RRID:CVCL_1233 | Homo sapiens (Human) | Glioblastoma | Population: Caucasian., Part of: COSMIC cell lines project., Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE). |
PMID:20164919 PMID:22460905 PMID:25984343 PMID:26589293 PMID:27397505 PMID:30894373 PMID:31068700 |
Cancer cell line | Male | GMS10 | CLO:CLO_0003547, ArrayExpress:E-MTAB-783, ArrayExpress:E-MTAB-2770, ArrayExpress:E-MTAB-3610, BioSample:SAMN03473583, BioSample:SAMN10988272, cancercelllines:CVCL_1233, Cell_Model_Passport:SIDM01074, ChEMBL-Cells:CHEMBL3308105, ChEMBL-Targets:CHEMBL1075449, Cosmic:687570, Cosmic:906873, Cosmic:1746948, Cosmic:2302331, Cosmic:2367528, Cosmic:2516018, Cosmic-CLP:906873, DepMap:ACH-000102, DSMZ:ACC-405, DSMZCellDive:ACC-405, EGA:EGAS00001000978, GDSC:906873, GEO:GSM326239, GEO:GSM887025, GEO:GSM888095, GEO:GSM1669812, IARC_TP53:21346, LiGeA:CCLE_764, LINCS_LDP:LCL-1352, PharmacoDB:GMS10_407_2019, Progenetix:CVCL_1233, PubChem_Cell_line:CVCL_1233, Wikidata:Q54854309 |
CVCL_1233 | 2026-07-25 04:38:17 | 0 | ||||
|
GM50334 Resource Report Resource Website |
RRID:CVCL_H996 | Homo sapiens (Human) | Cockayne syndrome | Finite cell line | Male | CLO:CLO_0012526, BioSample:SAMN00806855, Coriell:GM50334, Wikidata:Q54854273 |
CVCL_H996 | 2026-07-25 04:38:16 | 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 | 2026-07-25 04:38:16 | 0 | |||
|
GM50334 Resource Report Resource Website |
Coriell Cat# GM50334, RRID:CVCL_H996 | Homo sapiens (Human) | Cockayne syndrome | Finite cell line | Male | Coriell | GM50334 | CLO:CLO_0012526, BioSample:SAMN00806855, Coriell:GM50334, Wikidata:Q54854273 |
CVCL_H996 | 2026-07-25 04:38:16 | 0 | |||||
|
GM50284 Resource Report Resource Website |
RRID:CVCL_5T63 | Homo sapiens (Human) | Cri du chat syndrome | PMID:23665875 | Transformed cell line | Female | Coriell:GM50284, Wikidata:Q54854264 |
CVCL_5T63 | 2026-07-25 04:38:16 | 0 | ||||||
|
GM50186 Resource Report Resource Website |
Coriell Cat# GM50186, RRID:CVCL_0H55 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Female | JL430 | Coriell | GM50186 | CLO:CLO_0014983, Coriell:GM50186, Wikidata:Q54854252 |
CVCL_0H55 | 2026-07-25 04:38:16 | 0 | |||
|
GM50182 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM50182, RRID:CVCL_5T55 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | Coriell | GM50182 | Coriell:GM50182, Wikidata:Q54854251 |
CVCL_5T55 | 2026-07-25 04:38:16 | 0 | |||||
|
GM50188 Resource Report Resource Website |
RRID:CVCL_5T56 | Homo sapiens (Human) | Cri du chat syndrome | Population: Lebanese. | PMID:23665875 | Transformed cell line | Female | Coriell:GM50188, Wikidata:Q54854253 |
CVCL_5T56 | 2026-07-25 04:38:16 | 0 | |||||
|
GM50192 Resource Report Resource Website |
Coriell Cat# GM50192, RRID:CVCL_AB27 | Homo sapiens (Human) | Cri du chat syndrome | Transformed cell line | Female | JL446 | Coriell | GM50192 | CLO:CLO_0014998, Coriell:GM50192, Wikidata:Q54854255 |
CVCL_AB27 | 2026-07-25 04:38:16 | 0 | ||||
|
GM50291 Resource Report Resource Website |
Coriell Cat# GM50291, RRID:CVCL_2U68 | Homo sapiens (Human) | Transformed cell line | Male | JL612 | Coriell | GM50291 | CLO:CLO_0014977, Coriell:GM50291, Wikidata:Q54854265 |
CVCL_2U68 | 2026-07-25 04:38:16 | 0 | |||||
|
GMK-2 Resource Report Resource Website |
RRID:CVCL_L499 | Homo sapiens (Human) | Gastric adenocarcinoma | Population: Japanese., Part of: JFCR45 cancer cell line panel. |
PMID:14662023 PMID:15767549 |
Cancer cell line | Male | OKIBA | Wikidata:Q54854292 | CVCL_L499 | 2026-07-25 04:38:17 | 0 | ||||
|
GM50192 Resource Report Resource Website |
RRID:CVCL_AB27 | Homo sapiens (Human) | Cri du chat syndrome | Transformed cell line | Female | JL446 | CLO:CLO_0014998, Coriell:GM50192, Wikidata:Q54854255 |
CVCL_AB27 | 2026-07-25 04:38:16 | 0 | ||||||
|
GM50180 Resource Report Resource Website |
RRID:CVCL_5L35 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Male | JL393 | CLO:CLO_0014980, Coriell:GM50180, Wikidata:Q54854250 |
CVCL_5L35 | 2026-07-25 04:38:15 | 0 | |||||
|
GM50333 Resource Report Resource Website |
Coriell Cat# GM50333, RRID:CVCL_EG54 | Homo sapiens (Human) | Cockayne syndrome | Finite cell line | Male | Coriell | GM50333 | CLO:CLO_0012518, BioSample:SAMN00806853, Coriell:GM50333, Wikidata:Q54854272 |
CVCL_EG54 | 2026-07-25 04:38:16 | 0 | |||||
|
GM50248 Resource Report Resource Website |
Coriell Cat# GM50248, RRID:CVCL_5T60 | Homo sapiens (Human) | Cri du chat syndrome | PMID:23665875 | Transformed cell line | Male | Coriell | GM50248 | Coriell:GM50248, Wikidata:Q54854261 |
CVCL_5T60 | 2026-07-25 04:38:16 | 0 | ||||
|
GM50345 Resource Report Resource Website |
RRID:CVCL_H993 | Homo sapiens (Human) | Cerebrooculofacioskeletal syndrome | Finite cell line | Female | CLO:CLO_0012523, Coriell:GM50345, Wikidata:Q54854279 |
CVCL_H993 | 2026-07-25 04:38:16 | 0 | |||||||
|
GM50276 Resource Report Resource Website |
Coriell Cat# GM50276, RRID:CVCL_5T62 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Male | Coriell | GM50276 | Coriell:GM50276, Wikidata:Q54854263 |
CVCL_5T62 | 2026-07-25 04:38:16 | 0 | |||||
|
GM50180 Resource Report Resource Website |
Coriell Cat# GM50180, RRID:CVCL_5L35 | Homo sapiens (Human) | Deletion 18q syndrome | PMID:23665875 | Transformed cell line | Male | JL393 | Coriell | GM50180 | CLO:CLO_0014980, Coriell:GM50180, Wikidata:Q54854250 |
CVCL_5L35 | 2026-07-25 04:38:15 | 0 | |||
|
GM50215 Resource Report Resource Website |
Coriell Cat# GM50215, RRID:CVCL_5T59 | Homo sapiens (Human) | Cri du chat syndrome | PMID:23665875 | Transformed cell line | Female | Coriell | GM50215 | BioSample:SAMN00806849, Coriell:GM50215, Wikidata:Q54854260 |
CVCL_5T59 | 2026-07-25 04:38:16 | 0 | ||||
|
GM50189 Resource Report Resource Website |
Coriell Cat# GM50189, RRID:CVCL_4E22 | Homo sapiens (Human) | Transformed cell line | Female | JL438 | Coriell | GM50189 | CLO:CLO_0014994, Coriell:GM50189, Wikidata:Q54854254 |
CVCL_4E22 | 2026-07-25 04:38:16 | 0 |
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