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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM09772 Resource Report Resource Website |
RRID:CVCL_AL97 | Homo sapiens (Human) | Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. | Transformed cell line | Female | GM09772A | CLO:CLO_0030523, Coriell:GM09772, Wikidata:Q54844039 |
CVCL_AL97 | 2026-09-05 10:56:13 | 0 | ||||||
|
GM09816 Resource Report Resource Website |
RRID:CVCL_X474 | Homo sapiens (Human) | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0030665, Coriell:GM09816, Wikidata:Q54844074 |
CVCL_X474 | 2026-09-05 10:56:14 | 0 | |||||||
|
GM09824 Resource Report Resource Website |
RRID:CVCL_2N13 | Homo sapiens (Human) | PMID:23665875 | Finite cell line | Female | CLO:CLO_0030660, Coriell:GM09824, Wikidata:Q54844078 |
CVCL_2N13 | 2026-09-05 10:56:14 | 0 | |||||||
|
GM09850 Resource Report Resource Website |
RRID:CVCL_GT56 | Homo sapiens (Human) | Hereditary hemorrhagic telangiectasia | Transformed cell line | Female | CLO:CLO_0030629, Coriell:GM09850, Wikidata:Q54844090 |
CVCL_GT56 | 2026-09-05 10:56:14 | 0 | |||||||
|
GM09811 Resource Report Resource Website |
RRID:CVCL_IN25 | Homo sapiens (Human) | Neonatal hemochromatosis | Population: Caucasian; Portuguese. | PMID:2916654 | Finite cell line | Female | GM 09811 | CLO:CLO_0030458, Coriell:GM09811, Wikidata:Q54844066 |
CVCL_IN25 | 2026-09-05 10:56:14 | 0 | ||||
|
GM09773 Resource Report Resource Website |
RRID:CVCL_AL98 | Homo sapiens (Human) | Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. | Transformed cell line | Female | CLO:CLO_0030526, Coriell:GM09773, Wikidata:Q54844040 |
CVCL_AL98 | 2026-09-05 10:56:13 | 0 | |||||||
|
GM09771 Resource Report Resource Website |
Coriell Cat# GM17289, RRID:CVCL_N119 | Homo sapiens (Human) | Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection., Part of: Human variation panel., Part of: Genetic Testing Reference Material (GeT-RM) samples. |
PMID:20889555 PMID:29959025 |
Transformed cell line | Female | GM17289 | Coriell | GM17289 | CLO:CLO_0013077, CLO:CLO_0030524, Coriell:GM09771, Coriell:GM17289, GEO:GSM569759, GEO:GSM596353, GEO:GSM596771, GEO:GSM924891, Wikidata:Q54844038 |
CVCL_N119 | 2026-09-05 10:56:13 | 0 | |||
|
GM09764 Resource Report Resource Website |
RRID:CVCL_N118 | Homo sapiens (Human) | Population: Jewish; Ashkenazi., Part of: Human variation panel. | Transformed cell line | Female | GM09764A, GM17366 | CLO:CLO_0013709, CLO:CLO_0030543, Coriell:GM09764, Coriell:GM17366, Wikidata:Q54844030 |
CVCL_N118 | 2026-09-05 10:56:13 | 0 | ||||||
|
GM09783 Resource Report Resource Website |
Coriell Cat# GM09783, RRID:CVCL_AM08 | Homo sapiens (Human) | Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. | Transformed cell line | Female | Coriell | GM09783 | CLO:CLO_0030497, Coriell:GM09783, Wikidata:Q54844051 |
CVCL_AM08 | 2026-09-05 10:56:13 | 0 | |||||
|
GM09775 Resource Report Resource Website |
RRID:CVCL_AM00 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. | Transformed cell line | Female | CLO:CLO_0030520, Coriell:GM09775, Wikidata:Q54844042 |
CVCL_AM00 | 2026-09-05 10:56:13 | 0 | ||||||
|
GM09792 Resource Report Resource Website |
RRID:CVCL_AA97 | Homo sapiens (Human) | Familial dysautonomia | Population: Jewish; Ashkenazi. | Transformed cell line | Female | CLO:CLO_0030463, Coriell:GM09792, Wikidata:Q54844061 |
CVCL_AA97 | 2026-09-05 10:56:14 | 0 | ||||||
|
GM09774 Resource Report Resource Website |
RRID:CVCL_AL99 | Homo sapiens (Human) | Retinitis pigmentosa | Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. | Transformed cell line | Female | CLO:CLO_0030525, Coriell:GM09774, Wikidata:Q54844041 |
CVCL_AL99 | 2026-09-05 10:56:13 | 0 | ||||||
|
GM09834 Resource Report Resource Website |
Coriell Cat# GM09834, RRID:CVCL_2Z78 | Homo sapiens (Human) | Nevoid basal cell carcinoma syndrome | Population: Caucasian; Irish. | PMID:23665875 | Finite cell line | Female | GM09834A | Coriell | GM09834 | CLO:CLO_0030634, Coriell:GM09834, Wikidata:Q54844087 |
CVCL_2Z78 | 2026-09-05 10:56:14 | 0 | ||
|
GM09772 Resource Report Resource Website |
Coriell Cat# GM09772, RRID:CVCL_AL97 | Homo sapiens (Human) | Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. | Transformed cell line | Female | GM09772A | Coriell | GM09772 | CLO:CLO_0030523, Coriell:GM09772, Wikidata:Q54844039 |
CVCL_AL97 | 2026-09-05 10:56:13 | 0 | ||||
|
GM09794 Resource Report Resource Website |
Coriell Cat# GM09794, RRID:CVCL_AA99 | Homo sapiens (Human) | Population: Jewish; Ashkenazi. | Transformed cell line | Female | Coriell | GM09794 | CLO:CLO_0030465, Coriell:GM09794, Wikidata:Q54844063 |
CVCL_AA99 | 2026-09-05 10:56:14 | 0 | |||||
|
GM09776 Resource Report Resource Website |
Coriell Cat# GM09776, RRID:CVCL_AM01 | Homo sapiens (Human) | Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. | Transformed cell line | Female | Coriell | GM09776 | CLO:CLO_0030519, Coriell:GM09776, Wikidata:Q54844043 |
CVCL_AM01 | 2026-09-05 10:56:13 | 0 | |||||
|
GM09776 Resource Report Resource Website |
RRID:CVCL_AM01 | Homo sapiens (Human) | Population: Caucasian., Part of: Retinitis Pigmentosa Foundation Collection. | Transformed cell line | Female | CLO:CLO_0030519, Coriell:GM09776, Wikidata:Q54844043 |
CVCL_AM01 | 2026-09-05 10:56:13 | 0 | |||||||
|
GM09825 Resource Report Resource Website |
Coriell Cat# GM09825, RRID:CVCL_2N14 | Homo sapiens (Human) | Karyotypic information: 46,X,der(X)(Xpter->Xq21::Yq12->Yqter) (Coriell=GM09825). | Finite cell line | Female | Coriell | GM09825 | CLO:CLO_0030661, Coriell:GM09825, Wikidata:Q54844079 |
CVCL_2N14 | 2026-09-05 10:56:14 | 0 | |||||
|
GM09815 Resource Report Resource Website |
Coriell Cat# GM09815, RRID:CVCL_N120 | Homo sapiens (Human) | Population: Caucasian., Part of: Human variation panel. | Transformed cell line | Female | GM18045 | Coriell | GM09815 | CLO:CLO_0015623, CLO:CLO_0030663, Coriell:GM09815, Coriell:GM18045, Wikidata:Q54844073 |
CVCL_N120 | 2026-09-05 10:56:14 | 0 | ||||
|
GM09792 Resource Report Resource Website |
Coriell Cat# GM09792, RRID:CVCL_AA97 | Homo sapiens (Human) | Familial dysautonomia | Population: Jewish; Ashkenazi. | Transformed cell line | Female | Coriell | GM09792 | CLO:CLO_0030463, Coriell:GM09792, Wikidata:Q54844061 |
CVCL_AA97 | 2026-09-05 10:56:14 | 0 |
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