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 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM02215 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_JB88 | Homo sapiens (Human) | Autosomal dominant torsion dystonia 1 | Finite cell line | Male | GM-2215 | Coriell:GM02215, Wikidata:Q54837377 |
CVCL_JB88 | Cellosaurus | 2026-09-26 06:48:54 | 0 | ||||||
|
GM02328 Resource Report Resource Website |
Coriell Cat# GM02328, RRID:CVCL_DD69 | Homo sapiens (Human) | Osteogenesis imperfecta | Population: Caucasian. | PMID:6689020 | Finite cell line | Male | GM-2328, IMR-2328 | Coriell | GM02328 | CLO:CLO_0032180, BioSample:SAMN00807699, Coriell:GM02328, Wikidata:Q54837429 |
CVCL_DD69 | Cellosaurus | 2026-09-26 06:48:55 | 0 | ||
|
GM02307 Resource Report Resource Website |
Coriell Cat# GM02307, RRID:CVCL_4N24 | Homo sapiens (Human) | Autosomal recessive torsion dystonia 2 | Population: Caucasian. | Transformed cell line | Male | GM-2307 | Coriell | GM02307 | CLO:CLO_0032176, BioSample:SAMN00807683, Coriell:GM02307, Wikidata:Q54837421 |
CVCL_4N24 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||
|
GM02301 Resource Report Resource Website |
Coriell Cat# GM02301, RRID:CVCL_IL10 | Homo sapiens (Human) | Androgen insensitivity syndrome | Population: African American. | Finite cell line | Sex ambiguous | GM-2301 | Coriell | GM02301 | CLO:CLO_0032199, BioSample:SAMN00807671, Coriell:GM02301, Wikidata:Q54837415 |
CVCL_IL10 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||
|
GM02299 Resource Report Resource Website |
RRID:CVCL_IL08 | Homo sapiens (Human) | Androgen insensitivity syndrome | Population: African American. | Finite cell line | Sex ambiguous | GM-2299 | CLO:CLO_0032202, BioSample:SAMN00807667, Coriell:GM02299, Wikidata:Q54837413 |
CVCL_IL08 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||||
|
GM02305 Resource Report Resource Website |
RRID:CVCL_1U22 | Homo sapiens (Human) | Autosomal dominant torsion dystonia 1 | Population: Caucasian. | Transformed cell line | Female | GM-2305 | CLO:CLO_0032207, BioSample:SAMN00807679, Coriell:GM02305, Wikidata:Q54837419 |
CVCL_1U22 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||||
|
GM02229 Resource Report Resource Website |
Coriell Cat# GM02229, RRID:CVCL_4J48 | Homo sapiens (Human) | Transformed cell line | Female | GM-2229, GM02229A | Coriell | GM02229 | CLO:CLO_0032241, BioSample:SAMN00807616, Coriell:GM02229, Wikidata:Q54837383 |
CVCL_4J48 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||||
|
GM02230 Resource Report Resource Website |
RRID:CVCL_4J49 | Homo sapiens (Human) | Transformed cell line | Female | GM-2230 | CLO:CLO_0032244, BioSample:SAMN00807618, Coriell:GM02230, Wikidata:Q54837384 |
CVCL_4J49 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||||||
|
GM02205 Resource Report Resource Website Discontinued |
Coriell Cat# GM02205, RRID:CVCL_L968 | Homo sapiens (Human) | Population: Caucasian. |
PMID:6617268 PMID:23665875 PMID:24555846 PMID:25326100 |
Finite cell line | Male | GM-2205, GM 2205, GM01515 | Coriell | GM02205 | CLO:CLO_0032263, BioSample:SAMN00807602, Coriell:GM01515, Coriell:GM02205, GEO:GSM1266975, GEO:GSM1267054, GEO:GSM1288438, Wikidata:Q54837369 |
CVCL_L968 | Cellosaurus | 2026-09-26 06:48:53 | 0 | |||
|
GM02293 Resource Report Resource Website |
RRID:CVCL_M995 | Homo sapiens (Human) | Ehlers-Danlos syndrome | Population: Cuban., Part of: Human variation panel. | Finite cell line | Female | GM-2293, 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 | |||||
|
GM02304 Resource Report Resource Website 1+ mentions |
Coriell Cat# GM02304, RRID:CVCL_1U21 | Homo sapiens (Human) | Autosomal dominant torsion dystonia 1 | Population: Caucasian. | Finite cell line | Female | GM-2304 | Coriell | GM02304 | CLO:CLO_0032209, BioSample:SAMN00807677, Coriell:GM02304, Wikidata:Q54837418 |
CVCL_1U21 | Cellosaurus | 2026-09-26 06:48:54 | 1 | |||
|
GM02300 Resource Report Resource Website |
RRID:CVCL_IL09 | Homo sapiens (Human) | Androgen insensitivity syndrome | Population: African American. | Finite cell line | Sex ambiguous | GM-2300, GM02300A | CLO:CLO_0032203, BioSample:SAMN00807669, Coriell:GM02300, Wikidata:Q54837414 |
CVCL_IL09 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||||
|
GM02328 Resource Report Resource Website |
RRID:CVCL_DD69 | Homo sapiens (Human) | Osteogenesis imperfecta | Population: Caucasian. | PMID:6689020 | Finite cell line | Male | GM-2328, IMR-2328 | CLO:CLO_0032180, BioSample:SAMN00807699, Coriell:GM02328, Wikidata:Q54837429 |
CVCL_DD69 | Cellosaurus | 2026-09-26 06:48:55 | 0 | ||||
|
GM02211 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM02211, RRID:CVCL_JB67 | Homo sapiens (Human) | Wolman disease | PMID:6782865 | Finite cell line | Male | GM-2211, GM 2211, GM2211 | Coriell | GM02211 | Coriell:GM02211, Wikidata:Q54837374 |
CVCL_JB67 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||
|
GM02227 Resource Report Resource Website |
RRID:CVCL_L487 | Homo sapiens (Human) | Lesch-Nyhan syndrome |
PMID:3296189 PMID:6087154 |
Finite cell line | Male | GM-2227, GM 2227, GM2227 | CLO:CLO_0032249, Coriell:GM02227, Wikidata:Q54837381 |
CVCL_L487 | Cellosaurus | 2026-09-26 06:48:54 | 0 | |||||
|
GM02266 Resource Report Resource Website |
RRID:CVCL_BT13 | Homo sapiens (Human) | Beta thalassemia | Transformed cell line | Female | GM-2266, GM02266A | CLO:CLO_0032119, BioSample:SAMN00807642, Coriell:GM02266, Wikidata:Q54837398 |
CVCL_BT13 | Cellosaurus | 2026-09-26 06:48:54 | 0 | ||||||
|
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 |
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