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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM20738 Resource Report Resource Website |
RRID:CVCL_5R32 | Homo sapiens (Human) | Spondyloepimetaphyseal dysplasia with joint laxity type 2 | PMID:23665875 | Transformed cell line | Male | CLO:CLO_0028988, Coriell:GM20738, Wikidata:Q54851243 |
CVCL_5R32 | 2026-02-14 08:19:44 | 0 | ||||||
|
GM20916 Resource Report Resource Website |
RRID:CVCL_5R33 | Homo sapiens (Human) | Isodicentric chromosome | PMID:23665875 | Transformed cell line | Female | Coriell:GM20916, Wikidata:Q54851450 |
CVCL_5R33 | 2026-02-14 08:19:49 | 0 | ||||||
|
GM06563 Resource Report Resource Website |
RRID:CVCL_2T23 | Homo sapiens (Human) | Supernumerary circular chromosome | Population: Caucasian. | PMID:23665875 | Finite cell line | Female | CLO:CLO_0023243, Coriell:GM06563, Wikidata:Q54842302 |
CVCL_2T23 | 2026-02-14 08:16:07 | 0 | |||||
|
GM06526 Resource Report Resource Website |
RRID:CVCL_2T22 | Homo sapiens (Human) | Population: African American. | PMID:23665875 | Finite cell line | Male | CLO:CLO_0023240, Coriell:GM06526, Wikidata:Q54842297 |
CVCL_2T22 | 2026-02-14 08:16:07 | 0 | ||||||
|
GM06473 Resource Report Resource Website |
Coriell Cat# GM06473, RRID:CVCL_5N43 | Homo sapiens (Human) | Population: Hispanic. | PMID:23665875 | Finite cell line | Female | Coriell | GM06473 | CLO:CLO_0023251, Coriell:GM06473, Wikidata:Q54842293 |
CVCL_5N43 | 2026-02-14 08:16:06 | 0 | ||||
|
GM06563 Resource Report Resource Website |
Coriell Cat# GM06563, RRID:CVCL_2T23 | Homo sapiens (Human) | Supernumerary circular chromosome | Population: Caucasian. | PMID:23665875 | Finite cell line | Female | Coriell | GM06563 | CLO:CLO_0023243, Coriell:GM06563, Wikidata:Q54842302 |
CVCL_2T23 | 2026-02-14 08:16:07 | 0 | |||
|
GM06526 Resource Report Resource Website |
Coriell Cat# GM06526, RRID:CVCL_2T22 | Homo sapiens (Human) | Population: African American. | PMID:23665875 | Finite cell line | Male | Coriell | GM06526 | CLO:CLO_0023240, Coriell:GM06526, Wikidata:Q54842297 |
CVCL_2T22 | 2026-02-14 08:16:07 | 0 | ||||
|
GM06801 Resource Report Resource Website |
Coriell Cat# GM06801, RRID:CVCL_5N44 | Homo sapiens (Human) | Intellectual developmental disorder | Population: Caucasian. | PMID:23665875 | Transformed cell line | Female | Coriell | GM06801 | Coriell:GM06801, Wikidata:Q54842332 |
CVCL_5N44 | 2026-02-14 08:16:09 | 0 | |||
|
GM06803 Resource Report Resource Website |
Coriell Cat# GM06803, RRID:CVCL_5N46 | Homo sapiens (Human) | WAGR syndrome | PMID:23665875 | Transformed cell line | Male | Coriell | GM06803 | CLO:CLO_0036543, Coriell:GM06803, Wikidata:Q54842334 |
CVCL_5N46 | 2026-02-14 08:16:09 | 0 | ||||
|
GM06870 Resource Report Resource Website |
Coriell Cat# GM06870, RRID:CVCL_5N47 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | Coriell | GM06870 | CLO:CLO_0036508, Coriell:GM06870, Wikidata:Q54842357 |
CVCL_5N47 | 2026-02-14 08:16:10 | 0 | |||||
|
GM06936 Resource Report Resource Website |
RRID:CVCL_5N50 | Homo sapiens (Human) | Population: Caucasian. | PMID:23665875 | Transformed cell line | Female | CLO:CLO_0036463, Coriell:GM06936, Wikidata:Q54842397 |
CVCL_5N50 | 2026-02-14 08:16:11 | 0 | ||||||
|
GM06870 Resource Report Resource Website |
RRID:CVCL_5N47 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | CLO:CLO_0036508, Coriell:GM06870, Wikidata:Q54842357 |
CVCL_5N47 | 2026-02-14 08:16:10 | 0 | |||||||
|
GM06938 Resource Report Resource Website |
Coriell Cat# GM06938, RRID:CVCL_5N52 | Homo sapiens (Human) | WAGR syndrome | Population: Caucasian. |
PMID:2559742 PMID:23665875 |
Finite cell line | Male | GM6938, GM06938B, 6938 | Coriell | GM06938 | CLO:CLO_0036455, Coriell:GM06938, Wikidata:Q54842399 |
CVCL_5N52 | 2026-02-14 08:16:11 | 0 | ||
|
GM06938 Resource Report Resource Website |
RRID:CVCL_5N52 | Homo sapiens (Human) | WAGR syndrome | Population: Caucasian. |
PMID:2559742 PMID:23665875 |
Finite cell line | Male | GM6938, GM06938B, 6938 | CLO:CLO_0036455, Coriell:GM06938, Wikidata:Q54842399 |
CVCL_5N52 | 2026-02-14 08:16:11 | 0 | ||||
|
GM06979 Resource Report Resource Website |
Coriell Cat# GM06979, RRID:CVCL_5N54 | Homo sapiens (Human) | Karyotypic information: 92,XXYY.arr(1-22)x2,(XY)x1 (Coriell=GM06979)., Population: Caucasian. | PMID:23665875 | Finite cell line | Male | Coriell | GM06979 | CLO:CLO_0036450, Coriell:GM06979, Wikidata:Q54842419 |
CVCL_5N54 | 2026-02-14 08:16:11 | 0 | ||||
|
GM06960 Resource Report Resource Website |
Coriell Cat# GM06960, RRID:CVCL_5N53 | Homo sapiens (Human) | Karyotypic information: 46,X,i(X)(q22) (PubMed=10377420)., Population: African American. |
PMID:10377420 PMID:23665875 |
Finite cell line | Female | GM6960 | Coriell | GM06960 | CLO:CLO_0036461, Coriell:GM06960, Wikidata:Q54842405 |
CVCL_5N53 | 2026-02-14 08:16:11 | 0 | |||
|
GM07151 Resource Report Resource Website |
RRID:CVCL_X048 | Homo sapiens (Human) | Tetralogy of Fallot | Karyotypic information: 46,X,t(X;17)(p11.2;p11.2).arr(1-22,X)x2 (Coriell=GM07151)., Population: Caucasian. |
PMID:2498246 PMID:23665875 |
Finite cell line | Female | GM7151 | CLO:CLO_0036891, Coriell:GM07151, Wikidata:Q54842547 |
CVCL_X048 | 2026-02-14 08:16:15 | 0 | ||||
|
GM07212 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_5N58 | Homo sapiens (Human) | PMID:23665875 | Finite cell line | Female | Coriell:GM07212, Wikidata:Q54842579 |
CVCL_5N58 | 2026-02-14 08:16:15 | 0 | |||||||
|
GM07212 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM07212, RRID:CVCL_5N58 | Homo sapiens (Human) | PMID:23665875 | Finite cell line | Female | Coriell | GM07212 | Coriell:GM07212, Wikidata:Q54842579 |
CVCL_5N58 | 2026-02-14 08:16:15 | 0 | |||||
|
GM07106 Resource Report Resource Website |
RRID:CVCL_5N55 | Homo sapiens (Human) | PMID:23665875 | Finite cell line | Male | CLO:CLO_0036812, Coriell:GM07106, Wikidata:Q54842537 |
CVCL_5N55 | 2026-02-14 08:16:14 | 0 |
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