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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM10880 Resource Report Resource Website |
RRID:CVCL_1S06 | Homo sapiens (Human) | Group: Human/rodent somatic cell hybrid. | PMID:2535035 | Hybrid cell line | FUS-8:4-BE1 | CLO:CLO_0024118, Coriell:GM10880, Wikidata:Q54844714 |
cvcl_1n79 | CVCL_1S06 | 2026-09-12 05:34:07 | 0 | |||||
|
GM10915 Resource Report Resource Website |
RRID:CVCL_0R39 | Homo sapiens (Human) | Gaucher disease | Population: Caucasian; Italian. |
PMID:30497978 PMID:36130205 |
Finite cell line | Male | CLO:CLO_0023326, BioSample:SAMN00800338, Coriell:GM10915, Wikidata:Q54844733 |
CVCL_0R39 | 2026-09-12 05:34:07 | 0 | |||||
|
GM10954 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_5P31 | Homo sapiens (Human) | PMID:23665875 | Finite cell line | Female | CLO:CLO_0023357, BioSample:SAMN00800373, Coriell:GM10954, Wikidata:Q54844760 |
CVCL_5P31 | 2026-09-12 05:34:08 | 0 | |||||||
|
GM10949 Resource Report Resource Website |
RRID:CVCL_0Q27 | Homo sapiens (Human) | Thanatophoric dysplasia | Population: Caucasian. | Finite cell line | Female | CLO:CLO_0023352, BioSample:SAMN00800369, Coriell:GM10949, Wikidata:Q54844757 |
CVCL_0Q27 | 2026-09-12 05:34:08 | 0 | ||||||
|
GM10958 Resource Report Resource Website |
RRID:CVCL_2T95 | Homo sapiens (Human) | Population: Caucasian. | Transformed cell line | Female | CLO:CLO_0023372, BioSample:SAMN00800375, Coriell:GM10958, Wikidata:Q54844761 |
CVCL_2T95 | 2026-09-12 05:34:08 | 0 | |||||||
|
GM10889 Resource Report Resource Website |
Coriell Cat# GM10889, RRID:CVCL_1S08 | Homo sapiens (Human) | Characteristics: Hybrid for chromosome 17 mapping (PubMed=9441767)., Group: Human/rodent somatic cell hybrid. | PMID:9441767 | Hybrid cell line | DHA4 | Coriell | GM10889 | CLO:CLO_0023415, Coriell:GM10889, Wikidata:Q54844717 |
cvcl_f739 | CVCL_1S08 | 2026-09-12 05:34:07 | 0 | |||
|
GM10866 Resource Report Resource Website |
RRID:CVCL_W606 | Homo sapiens (Human) | Hunter syndrome | Transformed cell line | Male | CLO:CLO_0024137, BioSample:SAMN00800296, Coriell:GM10866, Wikidata:Q54844706 |
CVCL_W606 | 2026-09-12 05:34:07 | 0 | |||||||
|
GM10862 Resource Report Resource Website |
Coriell Cat# GM10862, RRID:CVCL_5B92 | Homo sapiens (Human) | Part of: CEPH/Utah pedigree cell line collection. |
PMID:15514893 PMID:20856902 |
Transformed cell line | Male | Coriell | GM10862 | CLO:CLO_0024087, BioSample:SAMN00800288, Coriell:GM10862, GEO:GSM30096, GEO:GSM420643, Wikidata:Q54844702 |
CVCL_5B92 | 2026-09-12 05:34:07 | 0 | ||||
|
GM10932 Resource Report Resource Website |
RRID:CVCL_5P28 | Homo sapiens (Human) | Population: Caucasian. | PMID:23665875 | Finite cell line | Male | CLO:CLO_0023315, BioSample:SAMN00800359, Coriell:GM10932, Wikidata:Q54844751 |
CVCL_5P28 | 2026-09-12 05:34:08 | 0 | ||||||
|
GM10960 Resource Report Resource Website |
Coriell Cat# GM10960, RRID:CVCL_2T96 | Homo sapiens (Human) | Karyotypic information: 46,XY,t(1;11)(1pter->1q31.2::11q25->11qter;11pter->11q25::1q31.2->1qter) (Coriell=GM10960)., Population: Caucasian. | Transformed cell line | Male | Coriell | GM10960 | CLO:CLO_0023370, BioSample:SAMN00800379, Coriell:GM10960, Wikidata:Q54844763 |
CVCL_2T96 | 2026-09-12 05:34:08 | 0 | |||||
|
GM10918 Resource Report Resource Website |
Coriell Cat# GM10918, RRID:CVCL_5P26 | Homo sapiens (Human) | PMID:23665875 | Transformed cell line | Female | Coriell | GM10918 | CLO:CLO_0023325, BioSample:SAMN00800340, Coriell:GM10918, Wikidata:Q54844734 |
CVCL_5P26 | 2026-09-12 05:34:07 | 0 | |||||
|
GM10930 Resource Report Resource Website |
Coriell Cat# GM10930, RRID:CVCL_AD75 | Homo sapiens (Human) | Population: Caucasian. | Transformed cell line | Female | Coriell | GM10930 | CLO:CLO_0023313, BioSample:SAMN00800354, Coriell:GM10930, Wikidata:Q54844749 |
CVCL_AD75 | 2026-09-12 05:34:08 | 0 | |||||
|
GM10876 Resource Report Resource Website |
Coriell Cat# GM10876, RRID:CVCL_F616 | Homo sapiens (Human) | Wolman disease | Transformed cell line | Sex unspecified | Coriell | GM10876 | CLO:CLO_0024122, Coriell:GM10876, Wikidata:Q54844712 |
CVCL_F616 | 2026-09-12 05:34:07 | 0 | |||||
|
GM10892 Resource Report Resource Website |
RRID:CVCL_0Q24 | Homo sapiens (Human) | Thanatophoric dysplasia | Population: Caucasian. | Finite cell line | Male | CLO:CLO_0023417, BioSample:SAMN00800312, Coriell:GM10892, Wikidata:Q54844719 |
CVCL_0Q24 | 2026-09-12 05:34:07 | 0 | ||||||
|
GM10888 Resource Report Resource Website |
RRID:CVCL_1S07 | Cricetulus griseus (Chinese hamster) | Characteristics: Hybrid for chromosome 22 mapping. Contains a complete copy of chromosome 22., Group: Human/rodent somatic cell hybrid. |
PMID:2276735 PMID:2395866 PMID:8314568 PMID:8661140 |
Hybrid cell line | KG-1, K1 | CLO:CLO_0023414, Coriell:GM10888, Wikidata:Q54844716 |
cvcl_v244 | CVCL_1S07 | 2026-09-12 05:34:07 | 0 | |||||
|
GM10903 Resource Report Resource Website |
RRID:CVCL_F146 | Homo sapiens (Human) | De Sanctis-Cacchione syndrome | Population: Mexican. |
PMID:10767341 PMID:22661500 |
Finite cell line | Female | CLO:CLO_0023395, BioSample:SAMN00800324, Coriell:GM10903, Wikidata:Q54844725 |
CVCL_F146 | 2026-09-12 05:34:07 | 0 | |||||
|
GM10923 Resource Report Resource Website |
Coriell Cat# GM17003, RRID:CVCL_7505 | Homo sapiens (Human) | Population: Caucasian; Northern European., Part of: Human variation panel. | Transformed cell line | Male | GM17003 | Coriell | GM17003 | CLO:CLO_0018042, CLO:CLO_0023329, BioSample:SAMN00800346, Coriell:GM10923, Coriell:GM17003, Wikidata:Q54844737 |
CVCL_7505 | 2026-09-12 05:34:08 | 0 | ||||
|
GM10861 Resource Report Resource Website |
Coriell Cat# GM10861, RRID:CVCL_R614 | Homo sapiens (Human) | Population: Caucasian; Utah residents with ancestry from Northern and Western Europe., Part of: International Histocompatibility Workshop cell lines., Part of: International Genome Sample Resource (1000 genomes project) cell lines., Part of: CEPH/Utah pedigree cell line collection. |
PMID:15514893 PMID:17122850 PMID:19043577 PMID:20856902 PMID:23676674 PMID:24924344 |
Transformed cell line | Female | CEPH-1362-NA10861, 1362-8574 | Coriell | GM10861 | CLO:CLO_0024094, BioSample:SAMN00800286, Coriell:GM10861, dbMHC:48654, GEO:GSM25464, GEO:GSM25465, GEO:GSM30076, GEO:GSM112508, GEO:GSM112788, GEO:GSM188785, GEO:GSM207766, GEO:GSM291619, GEO:GSM316438, GEO:GSM316439, GEO:GSM316440, GEO:GSM420641, GEO:GSM420642, GEO:GSM957418, IGSR:NA10861, IHW:IHW01135, IPD-IMGT/HLA:25932, Wikidata:Q54844701 |
CVCL_R614 | 2026-09-12 05:34:07 | 0 | |||
|
GM10876 Resource Report Resource Website |
RRID:CVCL_F616 | Homo sapiens (Human) | Wolman disease | Transformed cell line | Sex unspecified | CLO:CLO_0024122, Coriell:GM10876, Wikidata:Q54844712 |
CVCL_F616 | 2026-09-12 05:34:07 | 0 | |||||||
|
GM10871 Resource Report Resource Website |
RRID:CVCL_0R37 | Homo sapiens (Human) | Gaucher disease | Population: Jewish; Ashkenazi. | Transformed cell line | Female | CLO:CLO_0024127, BioSample:SAMN00800302, Coriell:GM10871, Wikidata:Q54844709 |
CVCL_0R37 | 2026-09-12 05:34:07 | 0 |
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