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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
HAP1 ACACA (-) 2 Resource Report Resource Website Discontinued |
RRID:CVCL_SB14 | Homo sapiens (Human) | Chronic myelogenous leukemia, BCR-ABL1 positive | Group: Haploid karyotype cell line. | Cancer cell line | Male | HZGHC004903c012, ACACA knockout cell line 16bp deletion | Horizon_Discovery:HZGHC004903c012, Wikidata:Q54872460 |
cvcl_y019 | CVCL_SB14 | 2026-08-15 04:35:18 | 0 | ||||
|
GM17731 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_H530 | Homo sapiens (Human) | Facioscapulohumeral muscular dystrophy 1 | Senescence: Capable of at least 32 PDL (Coriell=GM17731). | Finite cell line | Male | CLO:CLO_0016993, Coriell:GM17731, Wikidata:Q54849126 |
CVCL_H530 | 2026-08-15 04:32:50 | 0 | ||||||
|
GM17957 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM17957, RRID:CVCL_4D72 | Homo sapiens (Human) | Population: Caucasian; Amish. | Finite cell line | Male | Coriell | GM17957 | Coriell:GM17957, Wikidata:Q54849356 |
CVCL_4D72 | 2026-08-15 04:32:54 | 0 | |||||
|
GM17940 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_F206 | Homo sapiens (Human) | Facioscapulohumeral muscular dystrophy 1 | Finite cell line | Male | CLO:CLO_0016286, Coriell:GM17940, Wikidata:Q54849340 |
CVCL_F206 | 2026-08-15 04:32:54 | 0 | |||||||
|
GM17957 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_4D72 | Homo sapiens (Human) | Population: Caucasian; Amish. | Finite cell line | Male | Coriell:GM17957, Wikidata:Q54849356 |
CVCL_4D72 | 2026-08-15 04:32:54 | 0 | |||||||
|
GM17922 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_DA57 | Homo sapiens (Human) | Niemann-Pick disease, type C1 | PMID:12955717 | Finite cell line | Male | CLO:CLO_0016277, Coriell:GM17922, Wikidata:Q54849324 |
CVCL_DA57 | 2026-08-15 04:32:54 | 0 | ||||||
|
GM23340 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_F184 | Homo sapiens (Human) | Population: Caucasian., Part of: Personal Genome Project (PGP) cell line collection. | Induced pluripotent stem cell | Male | GM23340*A | Coriell:GM23340, SKIP:SKIP000179, SKIP:SKIP004356, Wikidata:Q54853012 |
cvcl_f185 | CVCL_F184 | 2026-08-15 04:34:15 | 0 | |||||
|
GM23280 Resource Report Resource Website 1+ mentions Possibly Discontinued |
Coriell Cat# GM23280, RRID:CVCL_F179 | Homo sapiens (Human) | Caution: May be identical to one of the many iPSC cell lines produced from HDF1388 by the Center for iPS Cell Research and Application (CiRA)., Population: Caucasian. | PMID:27264186 | Induced pluripotent stem cell | Female | GM23280A, GM23280*A | Coriell | GM23280 | Coriell:GM23280, SKIP:SKIP000387, SKIP:SKIP004353, Wikidata:Q54852964 |
cvcl_dp59 | CVCL_F179 | 2026-08-15 04:34:14 | 1 | ||
|
GM23394 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_F166 | Homo sapiens (Human) | Population: African American. | Induced pluripotent stem cell | Male | GM23394*B | Coriell:GM23394, SKIP:SKIP000180, SKIP:SKIP004359, Wikidata:Q54853048 |
cvcl_7477 | CVCL_F166 | 2026-08-15 04:34:15 | 0 | |||||
|
GM23394 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM23394, RRID:CVCL_F166 | Homo sapiens (Human) | Population: African American. | Induced pluripotent stem cell | Male | GM23394*B | Coriell | GM23394 | Coriell:GM23394, SKIP:SKIP000180, SKIP:SKIP004359, Wikidata:Q54853048 |
cvcl_7477 | CVCL_F166 | 2026-08-15 04:34:15 | 0 | |||
|
GM23778 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_4T52 | Homo sapiens (Human) | Ullrich congenital muscular dystrophy | Finite cell line | Male | Coriell:GM23778, Wikidata:Q54853303 |
CVCL_4T52 | 2026-08-15 04:34:21 | 0 | |||||||
|
GM23906 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_5T33 | Homo sapiens (Human) | Hyperglycerolemia | PMID:23665875 | Transformed cell line | Male | Coriell:GM23906, Wikidata:Q54853432 |
CVCL_5T33 | 2026-08-15 04:34:23 | 0 | ||||||
|
GM24224 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_4T59 | Homo sapiens (Human) | Ullrich congenital muscular dystrophy | Finite cell line | Male | Coriell:GM24224, Wikidata:Q54853641 |
CVCL_4T59 | 2026-08-15 04:34:28 | 0 | |||||||
|
GM24581 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM24581, RRID:CVCL_1N90 | Homo sapiens (Human) | Population: Caucasian. | Induced pluripotent stem cell | Female | GM24581*B | Coriell | GM24581 | Coriell:GM24581, SKIP:SKIP000664, Wikidata:Q54853785 |
cvcl_7348 | CVCL_1N90 | 2026-08-15 04:34:32 | 0 | |||
|
GM22232 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM22232, RRID:CVCL_1U26 | Homo sapiens (Human) | Population: Jewish; Ashkenazi., Part of: National Laboratory for the Genetics of Israeli Populations (NLGIP) collection. | Transformed cell line | Male | NLGIP-6630, NLGIP6630 | Coriell | GM22232 | CLO:CLO_0014821, Coriell:GM22232, Wikidata:Q54852442 |
CVCL_1U26 | 2026-08-15 04:34:03 | 0 | ||||
|
GM22931 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_5S34 | Homo sapiens (Human) | 1p36 deletion syndrome | PMID:23665875 | Transformed cell line | Male | Coriell:GM22931, Wikidata:Q54852836 |
CVCL_5S34 | 2026-08-15 04:34:11 | 0 | ||||||
|
GM18797 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_0X09 | Homo sapiens (Human) | Population: Chinese; Han in Beijing (CHB). | Transformed cell line | Male | Coriell:GM18797, Wikidata:Q54849852 |
CVCL_0X09 | 2026-08-15 04:33:08 | 0 | |||||||
|
GM18797 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM18797, RRID:CVCL_0X09 | Homo sapiens (Human) | Population: Chinese; Han in Beijing (CHB). | Transformed cell line | Male | Coriell | GM18797 | Coriell:GM18797, Wikidata:Q54849852 |
CVCL_0X09 | 2026-08-15 04:33:08 | 0 | |||||
|
HEK293/PTHR1/CRE/beta-lactamase Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_KA75 | Homo sapiens (Human) | Characteristics: Expresses beta-lactamase under the control of a CRE element (GenScript=M00148). | Transformed cell line | Female | HEK293/PTHR1/CRE/beta-Lac | GenScript:M00148, Wikidata:Q54882477 |
cvcl_0045 | CVCL_KA75 | 2026-08-15 04:37:24 | 0 | |||||
|
HEK293/NFAT/beta-lactamase Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_KA65 | Homo sapiens (Human) | Characteristics: Transfected with the 3xNFAT-beta-lactamase-Zeo plasmid containing a beta-lactamase reporter gene under control of the NFAT response element (GenScript=M00146). | Transformed cell line | Female | GenScript:M00146, Wikidata:Q54882474 |
cvcl_0045 | CVCL_KA65 | 2026-08-15 04:37:24 | 0 |
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