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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 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM02224 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM02224, RRID:CVCL_CX22 | Homo sapiens (Human) | Lactic acidosis | Finite cell line | Female | GM-2224 | Coriell | GM02224 | Coriell:GM02224, Wikidata:Q54837379 |
CVCL_CX22 | Cellosaurus | 2026-09-26 06:48:54 | 0 | ||||
|
GM02324 Resource Report Resource Website |
Coriell Cat# GM02324, RRID:CVCL_X261 | Homo sapiens (Human) | Karyotypic information: 46,XX,9qh+,t(16;22)(16qter->16p13.11::22q11.21->22qter;22pter->22q11.21::16p13.11->16pter) (Coriell=GM02324)., Population: Caucasian. | PMID:2714795 | Transformed cell line | Female | GM-2324, GM2324, GM02324A | Coriell | GM02324 | CLO:CLO_0032172, BioSample:SAMN00807693, Coriell:GM02324, Wikidata:Q54837426 |
CVCL_X261 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||
|
GM02293 Resource Report Resource Website |
Coriell Cat# GM17353, RRID:CVCL_M995 | Homo sapiens (Human) | Ehlers-Danlos syndrome | Population: Cuban., Part of: Human variation panel. | Finite cell line | Female | GM-2293, GM17353 | Coriell | GM17353 | CLO:CLO_0013723, CLO:CLO_0032132, BioSample:SAMN00807660, Coriell:GM02293, Coriell:GM17353, Wikidata:Q54837409 |
CVCL_M995 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||
|
GM02191 Resource Report Resource Website |
Coriell Cat# GM02191, RRID:CVCL_1H59 | Homo sapiens (Human) | Huntington's disease | Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease., Population: Caucasian. | Finite cell line | Female | GM-2191 | Coriell | GM02191 | CLO:CLO_0032264, BioSample:SAMN00807600, Coriell:GM02191, Wikidata:Q54837368 |
CVCL_1H59 | Cellosaurus | 2026-09-26 06:48:53 | 0 | |||
|
GM02214 Resource Report Resource Website |
RRID:CVCL_H179 | Homo sapiens (Human) | Metachromatic leukodystrophy | Donor information: At sampling donor was not affected with metachromatic leukodystrophy but at risk for disease., Population: Caucasian. | Finite cell line | Male | GM-2214 | CLO:CLO_0032259, BioSample:SAMN00807610, Coriell:GM02214, Wikidata:Q54837376 |
CVCL_H179 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||||
|
GM02295 Resource Report Resource Website |
RRID:CVCL_4T29 | Homo sapiens (Human) | Winchester syndrome | Population: Puerto Rican. | PMID:22922033 | Finite cell line | Female | GM-2295 | CLO:CLO_0032204, BioSample:SAMN00807665, Coriell:GM02295, Wikidata:Q54837411 |
CVCL_4T29 | Cellosaurus | 2026-09-26 06:48:54 | 0 | ||||
|
GM02317 Resource Report Resource Website |
Coriell Cat# GM02317, RRID:CVCL_8A67 | Homo sapiens (Human) | Population: Caucasian; Irish. |
PMID:21418647 PMID:24555846 PMID:25326100 |
Finite cell line | Female | GM-2317 | Coriell | GM02317 | CLO:CLO_0032170, BioSample:SAMN00807691, Coriell:GM02317, GEO:GSM651116, GEO:GSM651117, GEO:GSM1257698, GEO:GSM1266973, GEO:GSM1267052, GEO:GSM1288440, GEO:GSM1314048, Wikidata:Q54837425 |
CVCL_8A67 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||
|
GM02290 Resource Report Resource Website |
Coriell Cat# GM02290, RRID:CVCL_7356 | Homo sapiens (Human) | Lesch-Nyhan syndrome | Population: Caucasian. |
PMID:477417 PMID:6087472 |
Finite cell line | Male | GM-2290, GM 2290 GM02290A | Coriell | GM02290 | CLO:CLO_0003523, CLO:CLO_0032129, CLDB:cl1490, BioSample:SAMN00807654, Coriell:GM02290, Wikidata:Q54837406 |
CVCL_7356 | Cellosaurus | 2026-09-26 06:48:54 | 0 | ||
|
GM02299 Resource Report Resource Website |
Coriell Cat# GM02299, RRID:CVCL_IL08 | Homo sapiens (Human) | Androgen insensitivity syndrome | Population: African American. | Finite cell line | Sex ambiguous | GM-2299 | Coriell | GM02299 | CLO:CLO_0032202, BioSample:SAMN00807667, Coriell:GM02299, Wikidata:Q54837413 |
CVCL_IL08 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||
|
GM02302 Resource Report Resource Website |
RRID:CVCL_W226 | Homo sapiens (Human) | Hereditary coproporphyria | Population: Caucasian. | Transformed cell line | Female | GM-2302 | CLO:CLO_0032201, BioSample:SAMN00807673, Coriell:GM02302, Wikidata:Q54837416 |
CVCL_W226 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||||
|
GM02306 Resource Report Resource Website |
Coriell Cat# GM02306, RRID:CVCL_4N23 | Homo sapiens (Human) | Autosomal recessive torsion dystonia 2 | Population: Caucasian. | Finite cell line | Male | GM-2306 | Coriell | GM02306 | CLO:CLO_0032175, BioSample:SAMN00807681, Coriell:GM02306, Wikidata:Q54837420 |
CVCL_4N23 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||
|
GM02213 Resource Report Resource Website |
RRID:CVCL_4J47 | Homo sapiens (Human) | Acute intermittent porphyria | Population: Caucasian. | Transformed cell line | Female | GM-2213 | CLO:CLO_0032260, BioSample:SAMN00807608, Coriell:GM02213, Wikidata:Q54837375 |
CVCL_4J47 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||||
|
GM02317 Resource Report Resource Website |
RRID:CVCL_8A67 | Homo sapiens (Human) | Population: Caucasian; Irish. |
PMID:21418647 PMID:24555846 PMID:25326100 |
Finite cell line | Female | GM-2317 | CLO:CLO_0032170, BioSample:SAMN00807691, Coriell:GM02317, GEO:GSM651116, GEO:GSM651117, GEO:GSM1257698, GEO:GSM1266973, GEO:GSM1267052, GEO:GSM1288440, GEO:GSM1314048, Wikidata:Q54837425 |
CVCL_8A67 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||||
|
GM02268 Resource Report Resource Website |
Coriell Cat# GM02268, RRID:CVCL_W662 | Homo sapiens (Human) | Hunter syndrome | Population: Caucasian. | Finite cell line | Female | GM-2268, GM02268A | Coriell | GM02268 | CLO:CLO_0032121, BioSample:SAMN00807646, Coriell:GM02268, Wikidata:Q54837400 |
CVCL_W662 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||
|
GM02301 Resource Report Resource Website |
RRID:CVCL_IL10 | Homo sapiens (Human) | Androgen insensitivity syndrome | Population: African American. | Finite cell line | Sex ambiguous | GM-2301 | CLO:CLO_0032199, BioSample:SAMN00807671, Coriell:GM02301, Wikidata:Q54837415 |
CVCL_IL10 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||||
|
GM02438 Resource Report Resource Website |
Coriell Cat# GM02438, RRID:CVCL_IJ35 | Homo sapiens (Human) | Galactosialidosis | PMID:8910459 | Finite cell line | Female | GM02438A, GM02438a | Coriell | GM02438 | CLO:CLO_0033286, Coriell:GM02438, Wikidata:Q54837490 |
CVCL_IJ35 | Cellosaurus | 2026-09-26 06:48:56 | 0 | |||
|
GM02364 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM02364, RRID:CVCL_JD75 | Homo sapiens (Human) | Fanconi anemia | Finite cell line | Male | GM-2364 | Coriell | GM02364 | Coriell:GM02364, Wikidata:Q54837461 |
CVCL_JD75 | Cellosaurus | 2026-09-26 06:48:55 | 0 | ||||
|
GM02433 Resource Report Resource Website |
RRID:CVCL_CZ14 | Homo sapiens (Human) | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0033284, BioSample:SAMN00807769, Coriell:GM02433, Wikidata:Q54837485 |
CVCL_CZ14 | Cellosaurus | 2026-09-26 06:48:56 | 0 | |||||||
|
GM02338 Resource Report Resource Website |
Coriell Cat# GM02338, RRID:CVCL_D869 | Homo sapiens (Human) | Lesch-Nyhan syndrome | Population: Caucasian. | PMID:477417 | Finite cell line | Male | GM-2338 | Coriell | GM02338 | CLO:CLO_0033127, BioSample:SAMN00807719, Coriell:GM02338, Wikidata:Q54837439 |
CVCL_D869 | Cellosaurus | 2026-09-26 06:48:55 | 0 | ||
|
GM02329 Resource Report Resource Website |
Coriell Cat# GM02329, RRID:CVCL_X263 | Homo sapiens (Human) | Trisomy 9 | Karyotypic information: 47,XX,+9 [5]; 46,XX [45] (Coriell=GM02329)., Population: Caucasian. | PMID:6661932 | Finite cell line | Female | GM-2329, GM 2329 | Coriell | GM02329 | CLO:CLO_0033128, BioSample:SAMN00807701, Coriell:GM02329, Wikidata:Q54837430 |
CVCL_X263 | Cellosaurus | 2026-09-26 06:48:55 | 0 |
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