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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM03871 Resource Report Resource Website |
RRID:CVCL_1H76 | Homo sapiens (Human) | Population: Caucasian. | Transformed cell line | Female | CLO:CLO_0016030, BioSample:SAMN00808583, Coriell:GM03871, Wikidata:Q54838290 |
CVCL_1H76 | 2026-09-12 05:32:34 | 0 | |||||||
|
GM03893 Resource Report Resource Website |
RRID:CVCL_AK90 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian. | Finite cell line | Male | CLO:CLO_0016023, BioSample:SAMN00808598, Coriell:GM03893, Wikidata:Q54838306 |
CVCL_AK90 | 2026-09-12 05:32:34 | 0 | ||||||
|
GM03906 Resource Report Resource Website |
Coriell Cat# GM03906, RRID:CVCL_AK92 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian. | Finite cell line | Male | Coriell | GM03906 | CLO:CLO_0015983, Coriell:GM03906, Wikidata:Q54838315 |
CVCL_AK92 | 2026-09-12 05:32:34 | 0 | ||||
|
GM03904 Resource Report Resource Website |
Coriell Cat# GM03904, RRID:CVCL_IN21 | Homo sapiens (Human) | Neuropathy, hereditary sensory and autonomic, type IV | Population: Ecuadorian. | Finite cell line | Male | Coriell | GM03904 | CLO:CLO_0015979, Coriell:GM03904, Wikidata:Q54838313 |
CVCL_IN21 | 2026-09-12 05:32:34 | 0 | ||||
|
GM03900 Resource Report Resource Website |
RRID:CVCL_X050 | Homo sapiens (Human) | Familial adenomatous polyposis | Population: African American. |
PMID:3374507 PMID:6617268 |
Finite cell line | Female | GM 3900, GM3900 | CLO:CLO_0015987, Coriell:GM03900, Wikidata:Q54838310 |
CVCL_X050 | 2026-09-12 05:32:34 | 0 | ||||
|
GM03896 Resource Report Resource Website |
RRID:CVCL_9Z41 | Homo sapiens (Human) | Refsum disease | Population: Caucasian. | Finite cell line | Male | GM3896, GM03896A | CLO:CLO_0015985, Coriell:GM03896, Wikidata:Q54838308 |
CVCL_9Z41 | 2026-09-12 05:32:34 | 0 | |||||
|
GM03852 Resource Report Resource Website |
RRID:CVCL_GY20 | Homo sapiens (Human) | Leber congenital amaurosis | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0015628, BioSample:SAMN00808566, Coriell:GM03852, Wikidata:Q54838270 |
CVCL_GY20 | 2026-09-12 05:32:33 | 0 | ||||||
|
GM03912 Resource Report Resource Website |
RRID:CVCL_X114 | Homo sapiens (Human) | Cri du chat syndrome |
PMID:6617268 PMID:6661932 PMID:23665875 |
Finite cell line | Male | GM 3912 | CLO:CLO_0016130, Coriell:GM03912, Wikidata:Q54838319 |
CVCL_X114 | 2026-09-12 05:32:35 | 0 | |||||
|
GM03983 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_UY63 | Canis lupus familiaris (Dog) | Finite cell line | Male | Coriell:GM03983, Wikidata:Q93586605 |
CVCL_UY63 | 2026-09-12 05:32:35 | 0 | ||||||||
|
GM03932 Resource Report Resource Website |
RRID:CVCL_9S53 | Homo sapiens (Human) | Limb-girdle muscular dystrophy type 2A | Population: Caucasian. | Finite cell line | Male | CLO:CLO_0016132, Coriell:GM03932, Wikidata:Q54838331 |
CVCL_9S53 | 2026-09-12 05:32:35 | 0 | ||||||
|
GM03950 Resource Report Resource Website |
RRID:CVCL_CY39 | Homo sapiens (Human) | Familial adenomatous polyposis | Donor information: At sampling donor was not affected with familial adenomatous polyposis but at significant risk for disease., Population: Caucasian. | Finite cell line | Female | CLO:CLO_0016077, Coriell:GM03950, Wikidata:Q54838345 |
CVCL_CY39 | 2026-09-12 05:32:35 | 0 | ||||||
|
GM03989 Resource Report Resource Website |
RRID:CVCL_X127 | Homo sapiens (Human) | Dystrophia myotonica 1 | Population: Caucasian. | Finite cell line | Male | CLO:CLO_0016062, Coriell:GM03989, Wikidata:Q54838358 |
CVCL_X127 | 2026-09-12 05:32:35 | 0 | ||||||
|
GM04107 Resource Report Resource Website |
RRID:CVCL_9Q95 | Homo sapiens (Human) | LEOPARD syndrome | Population: Caucasian. | Finite cell line | Male | CLO:CLO_0016210, Coriell:GM04107, Wikidata:Q54838389 |
CVCL_9Q95 | 2026-09-12 05:32:36 | 0 | ||||||
|
GM04128 Resource Report Resource Website |
RRID:CVCL_0P44 | Homo sapiens (Human) | Hepatolenticular degeneration | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0016192, Coriell:GM04128, Wikidata:Q54838394 |
CVCL_0P44 | 2026-09-12 05:32:36 | 0 | ||||||
|
GM03978 Resource Report Resource Website |
RRID:CVCL_V241 | Canis lupus familiaris (Dog) | Finite cell line | Female | CLO:CLO_0016056, Coriell:GM03978, Wikidata:Q54838354 |
CVCL_V241 | 2026-09-12 05:32:35 | 0 | ||||||||
|
GM04045 Resource Report Resource Website |
Coriell Cat# GM04045, RRID:CVCL_X118 | Homo sapiens (Human) | Karyotypic information: 46,XY,t(2;4)(2pter->2q14::4q31.3->4qter;4pter->4q31.1::2q14->2qter) (Coriell=GM04045)., Population: Caucasian; Greek. |
PMID:6617268 PMID:6661932 |
Finite cell line | Male | GM-4045, GM 4045, GM04045B, GM 4045 B | Coriell | GM04045 | CLO:CLO_0016233, Coriell:GM04045, Wikidata:Q54838379 |
CVCL_X118 | 2026-09-12 05:32:36 | 0 | |||
|
GM04026 Resource Report Resource Website 1+ mentions |
Coriell Cat# GM04026, RRID:CVCL_AX77 | Homo sapiens (Human) | Fragile X syndrome | Population: Caucasian. | Finite cell line | Male | Coriell | GM04026 | CLO:CLO_0016230, Coriell:GM04026, Wikidata:Q54838375 |
CVCL_AX77 | 2026-09-12 05:32:36 | 1 | ||||
|
GM03954 Resource Report Resource Website |
RRID:CVCL_CY43 | Homo sapiens (Human) | Familial adenomatous polyposis | Population: Caucasian. | PMID:30024920 | Finite cell line | Male | CLO:CLO_0016094, Coriell:GM03954, Wikidata:Q54838349 |
CVCL_CY43 | 2026-09-12 05:32:35 | 0 | |||||
|
GM03945 Resource Report Resource Website |
RRID:CVCL_CY36 | Homo sapiens (Human) | Familial adenomatous polyposis | Population: Caucasian. | Transformed cell line | Female | CLO:CLO_0016113, Coriell:GM03945, Wikidata:Q54838340 |
CVCL_CY36 | 2026-09-12 05:32:35 | 0 | ||||||
|
GM03957 Resource Report Resource Website |
Coriell Cat# GM03957, RRID:CVCL_M947 | Homo sapiens (Human) | Population: Caucasian., Part of: Human variation panel. | Transformed cell line | Female | GM18014 | Coriell | GM03957 | CLO:CLO_0016015, CLO:CLO_0016091, Coriell:GM03957, Coriell:GM18014, Wikidata:Q54838352 |
CVCL_M947 | 2026-09-12 05:32:35 | 0 |
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