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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 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
GM16286 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A5WC | Homo sapiens (Human) | Facioscapulohumeral muscular dystrophy 1 | PMID:28161093 | Transformed cell line | Female | Coriell:GM16286, Wikidata:Q107115138 |
CVCL_A5WC | 2026-07-25 04:35:56 | 0 | ||||||
|
GM16287 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A5WD | Homo sapiens (Human) | Facioscapulohumeral muscular dystrophy 1 | PMID:28161093 | Transformed cell line | Male | Coriell:GM16287, Wikidata:Q107115140 |
CVCL_A5WD | 2026-07-25 04:35:56 | 0 | ||||||
|
GM16291 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A5WH | Homo sapiens (Human) | Facioscapulohumeral muscular dystrophy 1 | PMID:28161093 | Transformed cell line | Female | Coriell:GM16291, Wikidata:Q107115150 |
CVCL_A5WH | 2026-07-25 04:35:56 | 0 | ||||||
|
GM16295 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A5WL | Homo sapiens (Human) | PMID:28161093 | Transformed cell line | Male | Coriell:GM16295, Wikidata:Q107115158 |
CVCL_A5WL | 2026-07-25 04:35:56 | 0 | |||||||
|
GM16333 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_A5WM | Homo sapiens (Human) | Facioscapulohumeral muscular dystrophy 1 | PMID:28161093 | Transformed cell line | Female | Coriell:GM16333, Wikidata:Q107115161 |
CVCL_A5WM | 2026-07-25 04:35:57 | 0 | ||||||
|
GM16330 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM16330, RRID:CVCL_A5WR | Homo sapiens (Human) | PMID:28161093 | Transformed cell line | Sex unspecified | Coriell | GM16330 | Coriell:GM16330, Wikidata:Q107115159 |
CVCL_A5WR | 2026-07-25 04:35:57 | 0 | |||||
|
GM16436 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_0H58 | Homo sapiens (Human) | Tourette syndrome | Transformed cell line | Male | JL281 | Coriell:GM16436, Wikidata:Q54848558 |
CVCL_0H58 | 2026-07-25 04:35:59 | 0 | ||||||
|
GM16434 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM16434, RRID:CVCL_0H57 | Homo sapiens (Human) | Transformed cell line | Male | JL203 | Coriell | GM16434 | Coriell:GM16434, Wikidata:Q54848556 |
CVCL_0H57 | 2026-07-25 04:35:59 | 0 | |||||
|
GM16436 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM16436, RRID:CVCL_0H58 | Homo sapiens (Human) | Tourette syndrome | Transformed cell line | Male | JL281 | Coriell | GM16436 | Coriell:GM16436, Wikidata:Q54848558 |
CVCL_0H58 | 2026-07-25 04:35:59 | 0 | ||||
|
GM12059 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_4Z86 | Homo sapiens (Human) | X-linked ichthyosis | Finite cell line | Male | CLO:CLO_0020646, Coriell:GM12059, Wikidata:Q54845494 |
CVCL_4Z86 | 2026-07-25 04:34:47 | 0 | |||||||
|
GM12269 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_5D42 | Homo sapiens (Human) | Part of: CEPH/Utah pedigree cell line collection. | PMID:15514893 | Transformed cell line | Male | CLO:CLO_0019427, Coriell:GM12269, GEO:GSM25592, GEO:GSM30186, Wikidata:Q54845648 |
CVCL_5D42 | 2026-07-25 04:34:51 | 0 | ||||||
|
GM12236 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM12236, RRID:CVCL_9611 | Homo sapiens (Human) | Population: Caucasian; Utah residents with ancestry from Northern and Western Europe., Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. |
PMID:17122850 PMID:19797678 PMID:20398888 PMID:20856902 PMID:21397061 PMID:26621101 PMID:29474986 |
Transformed cell line | Female | CEPH-1408-NA12236, 1408-1019 | Coriell | GM12236 | CLO:CLO_0019202, EFO:EFO_0001143, Coriell:GM12236, dbMHC:48683, GEO:GSM25568, GEO:GSM25569, GEO:GSM112537, GEO:GSM112842, GEO:GSM273331, GEO:GSM273332, GEO:GSM314930, GEO:GSM314931, GEO:GSM420819, GEO:GSM420820, GEO:GSM486809, GEO:GSM486810, GEO:GSM648891, GEO:GSM659966, GEO:GSM660153, GEO:GSM660360, GEO:GSM905873, GEO:GSM905968, GEO:GSM906063, IHW:IHW01148, IPD-IMGT/HLA:25943, Wikidata:Q54845620 |
CVCL_9611 | 2026-07-25 04:34:50 | 0 | |||
|
GM12236 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_9611 | Homo sapiens (Human) | Population: Caucasian; Utah residents with ancestry from Northern and Western Europe., Part of: International Histocompatibility Workshop cell lines., Part of: CEPH/Utah pedigree cell line collection. |
PMID:17122850 PMID:19797678 PMID:20398888 PMID:20856902 PMID:21397061 PMID:26621101 PMID:29474986 |
Transformed cell line | Female | CEPH-1408-NA12236, 1408-1019 | CLO:CLO_0019202, EFO:EFO_0001143, Coriell:GM12236, dbMHC:48683, GEO:GSM25568, GEO:GSM25569, GEO:GSM112537, GEO:GSM112842, GEO:GSM273331, GEO:GSM273332, GEO:GSM314930, GEO:GSM314931, GEO:GSM420819, GEO:GSM420820, GEO:GSM486809, GEO:GSM486810, GEO:GSM648891, GEO:GSM659966, GEO:GSM660153, GEO:GSM660360, GEO:GSM905873, GEO:GSM905968, GEO:GSM906063, IHW:IHW01148, IPD-IMGT/HLA:25943, Wikidata:Q54845620 |
CVCL_9611 | 2026-07-25 04:34:50 | 0 | |||||
|
GM12408 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM12408, RRID:CVCL_5D91 | Homo sapiens (Human) | Part of: CEPH/Utah pedigree cell line collection. | Transformed cell line | Male | Coriell | GM12408 | CLO:CLO_0019806, BioSample:SAMN00801499, Coriell:GM12408, Wikidata:Q54845751 |
CVCL_5D91 | 2026-07-25 04:34:54 | 0 | |||||
|
GM12507 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM12507, RRID:CVCL_5U25 | Homo sapiens (Human) | Miller-Dieker syndrome | Finite cell line | Male | Coriell | GM12507 | CLO:CLO_0017439, Coriell:GM12507, Wikidata:Q54845814 |
CVCL_5U25 | 2026-07-25 04:34:56 | 0 | |||||
|
GM16733 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_YP91 | Homo sapiens (Human) | Population: Caucasian. | PMID:23661601 | Finite cell line | Female | Coriell:GM16733, Wikidata:Q93847995 |
CVCL_YP91 | 2026-07-25 04:36:01 | 0 | ||||||
|
GM16733 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM16733, RRID:CVCL_YP91 | Homo sapiens (Human) | Population: Caucasian. | PMID:23661601 | Finite cell line | Female | Coriell | GM16733 | Coriell:GM16733, Wikidata:Q93847995 |
CVCL_YP91 | 2026-07-25 04:36:01 | 0 | ||||
|
GM16735 Resource Report Resource Website Possibly Discontinued |
Coriell Cat# GM16735, RRID:CVCL_YP92 | Homo sapiens (Human) | Population: Caucasian. | PMID:23661601 | Finite cell line | Male | Coriell | GM16735 | Coriell:GM16735, Wikidata:Q93848015 |
CVCL_YP92 | 2026-07-25 04:36:01 | 0 | ||||
|
GM17397 Resource Report Resource Website Possibly Discontinued |
RRID:CVCL_9Z53 | Homo sapiens (Human) | Peroxisome biogenesis disorder 7B | PMID:16257970 | Finite cell line | Female | Coriell:GM17397, Wikidata:Q54848828 |
CVCL_9Z53 | 2026-07-25 04:36:03 | 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 | 2026-07-25 04:36:08 | 0 |
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