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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM25434 Resource Report Resource Website |
RRID:CVCL_HQ33 | Homo sapiens (Human) | Chromosome 16p12.1 deletion syndrome | Population: Caucasian. | Transformed cell line | Female | Coriell:GM25434, Wikidata:Q54853960 |
CVCL_HQ33 | 2026-07-25 04:37:54 | 0 | ||||||
|
GM25448 Resource Report Resource Website |
RRID:CVCL_HQ37 | Homo sapiens (Human) | Chromosome 16p12.1 deletion syndrome | Population: Caucasian. | Transformed cell line | Female | Coriell:GM25448, Wikidata:Q54853972 |
CVCL_HQ37 | 2026-07-25 04:37:55 | 0 | ||||||
|
GM25420 Resource Report Resource Website |
RRID:CVCL_EH26 | Homo sapiens (Human) | Choroideremia | Transformed cell line | Male | Coriell:GM25420, Wikidata:Q54853949 |
CVCL_EH26 | 2026-07-25 04:37:54 | 0 | |||||||
|
GM25435 Resource Report Resource Website |
Coriell Cat# GM25435, RRID:CVCL_HQ34 | Homo sapiens (Human) | Population: Caucasian. | Transformed cell line | Male | Coriell | GM25435 | Coriell:GM25435, Wikidata:Q54853961 |
CVCL_HQ34 | 2026-07-25 04:37:54 | 0 | |||||
|
GM25451 Resource Report Resource Website |
RRID:CVCL_HQ40 | Homo sapiens (Human) | Chromosome 16p12.1 deletion syndrome | Population: Caucasian. | Transformed cell line | Male | Coriell:GM25451, Wikidata:Q54853975 |
CVCL_HQ40 | 2026-07-25 04:37:55 | 0 | ||||||
|
GM25444 Resource Report Resource Website |
Coriell Cat# GM25444, RRID:CVCL_CX90 | Homo sapiens (Human) | Population: Chinese. | Finite cell line | Male | Coriell | GM25444 | Coriell:GM25444, Wikidata:Q54853969 |
CVCL_CX90 | 2026-07-25 04:37:55 | 0 | |||||
|
GM25428 Resource Report Resource Website |
RRID:CVCL_LN95 | Homo sapiens (Human) | Intellectual developmental disorder, autosomal dominant 1 | Transformed cell line | Female | Coriell:GM25428, Wikidata:Q54853954 |
CVCL_LN95 | 2026-07-25 04:37:54 | 0 | |||||||
|
GM25450 Resource Report Resource Website |
Coriell Cat# GM25450, RRID:CVCL_HQ39 | Homo sapiens (Human) | Chromosome 16p12.1 deletion syndrome | Population: Caucasian. | Transformed cell line | Female | Coriell | GM25450 | Coriell:GM25450, Wikidata:Q54853974 |
CVCL_HQ39 | 2026-07-25 04:37:55 | 0 | ||||
|
GM25453 Resource Report Resource Website |
Coriell Cat# GM25453, RRID:CVCL_HQ42 | Homo sapiens (Human) | Population: Caucasian. | Transformed cell line | Female | Coriell | GM25453 | Coriell:GM25453, Wikidata:Q54853977 |
CVCL_HQ42 | 2026-07-25 04:37:55 | 0 | |||||
|
GM25411 Resource Report Resource Website |
RRID:CVCL_HQ25 | Homo sapiens (Human) | Transformed cell line | Female | Coriell:GM25411, Wikidata:Q54853938 |
CVCL_HQ25 | 2026-07-25 04:37:54 | 0 | ||||||||
|
GM25433 Resource Report Resource Website |
RRID:CVCL_HQ32 | Homo sapiens (Human) | Chromosome 16p12.1 deletion syndrome | Population: Caucasian. | Transformed cell line | Female | Coriell:GM25433, Wikidata:Q54853959 |
CVCL_HQ32 | 2026-07-25 04:37:54 | 0 | ||||||
|
GM25413 Resource Report Resource Website |
Coriell Cat# GM25413, RRID:CVCL_HQ26 | Homo sapiens (Human) | Chromosome 16p12.1 deletion syndrome | Transformed cell line | Female | Coriell | GM25413 | Coriell:GM25413, Wikidata:Q54853940 |
CVCL_HQ26 | 2026-07-25 04:37:54 | 0 | |||||
|
GM25437 Resource Report Resource Website |
RRID:CVCL_HQ36 | Homo sapiens (Human) | Population: Caucasian. | Transformed cell line | Male | Coriell:GM25437, Wikidata:Q54853963 |
CVCL_HQ36 | 2026-07-25 04:37:55 | 0 | |||||||
|
GM25422 Resource Report Resource Website |
RRID:CVCL_HK69 | Homo sapiens (Human) | Choroideremia | Transformed cell line | Male | Coriell:GM25422, Wikidata:Q54853952 |
CVCL_HK69 | 2026-07-25 04:37:54 | 0 | |||||||
|
GM25498 Resource Report Resource Website |
RRID:CVCL_HK65 | Homo sapiens (Human) | Transformed cell line | Female | Coriell:GM25498, Wikidata:Q54853995 |
CVCL_HK65 | 2026-07-25 04:37:55 | 0 | ||||||||
|
GM25455 Resource Report Resource Website |
RRID:CVCL_BA16 | Homo sapiens (Human) | Rett syndrome | Population: Jewish; Ashkenazi. | Transformed cell line | Female | Coriell:GM25455, Wikidata:Q54853979 |
CVCL_BA16 | 2026-07-25 04:37:55 | 0 | ||||||
|
GM25421 Resource Report Resource Website |
RRID:CVCL_EH27 | Homo sapiens (Human) | Choroideremia | Finite cell line | Male | Coriell:GM25421, Wikidata:Q54853951 |
CVCL_EH27 | 2026-07-25 04:37:54 | 0 | |||||||
|
GM25454 Resource Report Resource Website |
RRID:CVCL_HQ43 | Homo sapiens (Human) | Population: Caucasian. | Transformed cell line | Female | Coriell:GM25454, Wikidata:Q54853978 |
CVCL_HQ43 | 2026-07-25 04:37:55 | 0 | |||||||
|
GM25412 Resource Report Resource Website |
RRID:CVCL_HL86 | Homo sapiens (Human) | Transformed cell line | Female | Coriell:GM25412, Wikidata:Q54853939 |
CVCL_HL86 | 2026-07-25 04:37:54 | 0 | ||||||||
|
GM25433 Resource Report Resource Website |
Coriell Cat# GM25433, RRID:CVCL_HQ32 | Homo sapiens (Human) | Chromosome 16p12.1 deletion syndrome | Population: Caucasian. | Transformed cell line | Female | Coriell | GM25433 | Coriell:GM25433, Wikidata:Q54853959 |
CVCL_HQ32 | 2026-07-25 04:37:54 | 0 |
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